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Review

Immune Checkpoint Blockade in Advanced Cutaneous Squamous Cell Carcinoma: What Do We Currently Know in 2020?

by
Anja Wessely
1,2,
Theresa Steeb
1,2,
Ulrike Leiter
3,
Claus Garbe
3,
Carola Berking
1,2,† and
Markus Vincent Heppt
1,2,*,†
1
Department of Dermatology, Deutsches Zentrum Immuntherapie (DZI), Universitätsklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany
2
Comprehensive Cancer Center Erlangen-European Metropolitan Area of Nuremberg (CCC ER-EMN), 91054 Erlangen, Germany
3
Department of Dermatology, Eberhard Karls University of Tübingen, 72074 Tübingen, Germany
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Int. J. Mol. Sci. 2020, 21(23), 9300; https://doi.org/10.3390/ijms21239300
Submission received: 31 October 2020 / Revised: 30 November 2020 / Accepted: 3 December 2020 / Published: 6 December 2020
(This article belongs to the Special Issue Cancer Immunotherapy Using Checkpoint Inhibitors: Future Directions 2.0)
Versions Notes

Abstract

:
Cutaneous squamous cell carcinoma (cSCC) is the second most common skin cancer that predominantly arises in chronically sun-damaged skin. Immunosuppression, genetic disorders such as xeroderma pigmentosum (XP), exposure to certain drugs and environmental noxae have been identified as major risk factors. Surgical removal of cSCC is the therapy of choice and mostly curative in early stages. However, a minority of patients develop locally advanced tumors or distant metastases that are still challenging to treat. Immune checkpoint blockade (ICB) targeting CTLA-4, PD-L1 and PD-1 has tremendously changed the field of oncological therapy and especially the treatment of skin cancers as tumors with a high mutational burden. In this review, we focus on the differences between cSCC and cutaneous melanoma (CM) and their implications on therapy, summarize the current evidence on ICB for the treatment of advanced cSCC and discuss the chances and pitfalls of this therapy option for this cancer entity. Furthermore, we focus on special subgroups of interest such as organ transplant recipients, patients with hematologic malignancies, XP and field cancerization.

1. Introduction

Cutaneous squamous cell carcinoma (cSCC) represents globally the second most common skin cancer after basal cell carcinoma (BCC) [1]. It derives from atypic keratinocytes located in the stratified squamous epithelium in the upper layers of the skin. The accumulation of genetic aberrations is thought to occur in a multistep process leading to the development of actinic keratoses (AK), which eventually progress to cSCC [2], although the risk is presumably low for single lesions. The presence of multiple AK and additional signs of chronic UV damage in the adjacent skin increases the risk for progression considerably [3,4,5]. Reported cSCC incidence rates range from 20 per 100,000 person-years (PYs) in Norway to 387 per 100,000 PYs in Australia [6], and over the last 40 years, the incidence has steadily increased in most countries [7,8]. Although this trend seems to have plateaued in Australia and the US as recently shown by Stang et al., incidence rates still increase strongly with age in all countries [8].
cSCC is most commonly present in elderly people with fair skin and arises particularly at sites that were long-term exposed to UV light, such as the scalp, face, ears and upper extremities [9,10,11]. Immunocompromised patients including solid organ transplant recipients (OTRs) [12], HIV-positive patients [13] and patients with chronic lymphatic leukemia [14,15] also have an increased risk for developing cSCC, indicating that an impaired immune system can promote cSCC development. UV light mediates beneficial effects such as vitamin D production, regulation of the central hypothalamic-pituitary-adrenal axis and increase in β-endorphin levels [16]. However, it contributes to skin carcinogenesis in two different ways. On the one hand, UV-B light causes characteristic transitions of cytosine to thymine in UV-damaged DNA. This mutational pattern is found for instance in TP53, the most commonly mutated gene in cSCC, which codes for the tumor suppressor p53 [17]. On the other hand, the immunosuppressive effect of UV-A can also contribute to cSCC formation [18]. Patients with impaired DNA repair caused by rare familial syndromes such as xeroderma pigmentosum (XP) also commonly develop cSCC [19]. Interestingly, a higher number of cSCC has been observed in patients who had received the hedgehog inhibitor vismodegib for BCC therapy or single agent BRAF inhibitors such as vemurafenib for melanoma therapy [20,21]. Moreover, in recent studies, it was observed that AK patients treated with ingenol mebutate developed more cSCC compared to other treatment options and consequently, the European Medicines Agency (EMA) withdrew the marketing authorization of this substance [22,23,24]. Additionally, environmental noxae as arsenic, nitrosamines, alkylating agents and polycyclic aromatic hydrocarbons have been identified as risk factors for developing cSCC [25]. Notably, cSCC arising in previously irradiated or burned skin are usually more aggressive than those arising in sun-damaged skin [26].
Surgical removal of cSCC is the therapy of choice and mostly curative in early stages [27]. However, a subset of patients develops locally advanced tumors or distant metastases that are challenging to treat. Larger high-quality studies and treatment recommendations especially for systemic therapy of advanced cSCC stages are scarce as lymphogenic or haematogenic metastasis only occurs in a minority of patients. Chemotherapy and epidermal growth factor receptor (EGFR) inhibitors have shown limited response as reported in the few available trials [28]. Most of the affected patients are also relatively old and suffer from multiple comorbidities. Hence, patients with locally advanced cSCC and distant metastases still have a very poor prognosis [29,30].
Immune checkpoint blockade (ICB) targeting CTLA-4, PD-L1 and PD-1 have tremendously changed the field of oncological therapy including particularly skin cancers as tumors with a high mutational burden. ICB has not only been successfully applied in melanoma [31] but also in non-small cell lung cancer (NSCLC) [32] and head and neck squamous cell carcinoma (HNSCC) [33]. Thus, the expectations were sufficiently high for a similar efficacy to be achieved in advanced cSCC as well.
In this review, we focus on the differences between cSCC and cutaneous melanoma (CM) and the resulting implications for prognosis, summarize the current evidence on ICB for the treatment of advanced cSCC and discuss the advantages and pitfalls of this therapy option for this cancer entity.

2. cSCC vs. CM: Genetic Differences and Implications for Prognosis

The cells of origin of both cSCC and CM reside in the epidermis, the top layer of the skin. Although being located within the same organ, these cells have distinct physiologic functions and are derived from precursor cells of different embryonic origin. cSCC arises from epidermal keratinocytes which are the main cell type building the skin barrier that protects underlying tissues against mechanical stress, chemicals, water loss and infections with viruses, bacteria, fungi and parasites [34]. They terminally differentiate into corneocytes that lack cell organelles and the nucleus and are, therefore, unable to proliferate [34]. Due to their localization, these cells are exposed to a variety of physical and chemical noxae including UV radiation. Melanocytes are pigment-producing cells residing near the basal layer of the epidermis, and they are the cells of origin of melanoma [35]. They are characterized by their typical shape with long protrusions (dendrites) and the presence of melanosomes [36]. These cell organelles contain a brownish pigment composed of one of two types of melanin, eumelanin (brown to black) or pheomelanin (yellow to red), and the ratio of eumelanin:pheomelanin determines the pigmentation of the skin [37,38]. Both melanin pigments are synthesized in a multistep cascade involving several enzymes based on the common precursor dopaquinone that is generated from the amino acid tyrosine [37]. Melanin is distributed by one melanocyte to about 30 surrounding keratinocytes [39], which take up this pigment and drape it around their nuclei as “sunscreen” to protect the DNA from UV-induced damage [35]. Eumelanin mediates the photoprotective effects, whereas degradation of the photolabile pheomelanin leads to the generation of reactive oxygen species including superoxide, hydrogen peroxide and hydroxyl radicals, which can result in additional DNA damage [40,41,42]. Fair-skinned individuals with red hair have a higher proportion of pheomelanin compared to individuals with darker skin and they have a higher risk for developing melanoma and non-melanoma skin cancer (NMSC) [40,43].
UV light stimulates melanin formation (melanogenesis) in a para-, auto- and even intracrine fashion, resulting in tanning of the skin [16]. In particular, exposure to UV-B light increases the expression of several proteins that are involved in pigmentation regulation including the G-protein-coupled melanocortin 1 receptor (MC1R), corticotropin-releasing hormone, urocortin and proopiomelanocortin (POMC) as well as the production of alpha melanocyte-stimulating hormone (α-MSH), adrenocorticotropic hormone (ACTH) and β-endorphin, which are generated by cleavage of their common precursor POMC [16,44]. POMC is mostly produced in the pituitary gland, but also directly in the skin by both keratinocytes and melanocytes and in other peripheral tissues [45,46].
Eumelanin production is stimulated by the binding of α-MSH and ACTH to their receptor MC1R, whereas agouti signaling protein (ASIP) favors the production of pheomelanin by affecting the binding of α-MSH to MC1R [38,40,47]. MC1R activation leads to increased intracellular cAMP levels as well as an increased phosphorylation and activation of CREB transcription factors [38,40]. Together with other transcription factors such as SOX10 and PAX3, they activate the transcription of genes that are involved in melanin synthesis—e.g., MITF, the master regulator of pigmentation [38,40]. Transcription factors such as MITF and SOX10 control the expression of enzymes involved in melanogenesis and also play a role in melanoma formation and progression [38]. Apart from POMC and its derivatives, which can also act in melanocytes in an intracrine manner, keratinocytes secrete a variety of factors including prostaglandin E2 and growth factors such as hepatocyte growth factor (HGF), stem cell factor (SCF), fibroblast growth factor (FGF), endothelin-1 in response to UV exposition to stimulate cell proliferation, differentiation and melanogenesis of adjacent melanocytes [41,47]. In addition, melanogenesis can be further influenced via estrogen, adrenergic and muscarinic receptors that are also able to increase intracellular cAMP levels in melanocytes [38,41,48]. Interestingly, keratinocytes and melanocytes are derived from precursor cells of different embryonic origin. Both keratinocytes and melanocytes are cells of ectodermal origin; however, the melanocyte precursors are originally located in the neural crest next to the neural tube. These cells migrate actively into the epidermis of the fetus at 12 weeks of gestation, where they develop into mature melanocytes [49]. The different embryonic origin at least partly explains the distinct aggressiveness and tendency to develop metastases. Cancer cells can re-express proteins that are exclusively expressed during embryogenesis [50]. In the case of melanoma, the tumor cells can acquire a migratory, invading phenotype suitable for forming metastasis by re-expressing proteins which are usually expressed exclusively during skin development. This phenomenon has been demonstrated for instance for the neural crest transcription factors Brn3a and recently for MSX1 [51,52], which both contribute to melanoma progression.
Although keratinocytes and melanocytes are exposed to UV light and environmental noxae in a similar manner, the impact on cSCC and melanoma formation is slightly different. cSCC mostly arises in chronically sun-damaged skin areas after long-term UV exposure over decades, while carcinogenic agents such as polycyclic aromatic hydrocarbons and arsenic can also contribute [6,53]. In contrast, melanoma arises both in sites with intermittent sun exposure [53,54] and in chronically sun-damaged areas. In comparison to cSCC, environmental noxae as well as UV light play a minor role in melanoma pathogenesis. Despite all these differences, both skin cancer entities comprise tumors with a high mutational burden which seems to be a major reason for a good response to ICB [55].

3. ICB in cSCC: What Is the Current Evidence?

ICB intends to boost the intrinsic anti-tumor immune response by blocking mechanisms that counteract overwhelming immune responses. The pioneering results in difficult-to-treat cancers such as melanoma and other squamous cell carcinoma including NSCLC and HNSCC have brought ICB into the focus of cSCC research. Over the last couple of years, immune checkpoint-blocking antibodies have been investigated in several trials. The first hints for a probable success of ICB in cSCC were initially described in case reports of melanoma patients coincidentally diagnosed with cSCC, who had received ICB and subsequently responded [56]. Today, most evidence for the efficacy of ICB in advanced cSCC is available for anti-PD-1 antibodies.

3.1. Anti-CTLA-4 Antibody: Ipilimumab

Day et al. reported the case of a metastatic cSCC patient who had been diagnosed coincidentally with metastatic BRAFG469E-mutated melanoma and, therefore, received ipilimumab every 3 weeks (Q3W, no dosage reported) for 4 cycles [56]. The patient showed a decrease in the cSCC metastases after three cycles of ipilimumab and achieved a partial response (PR) (Table 1). At the time of publication, the progression-free survival (PFS) was 8 months. No adverse events (AEs) ≥ grade 3 were reported. The authors described the quality of life to be excellent.

3.2. Anti-PD-1-Blocking Antibodies

3.2.1. Nivolumab

One case series and some case reports represent the only available evidence for the efficacy of nivolumab in cSCC. The retrospective case series described five advanced NMSC patients who were treated with PD-1 blocking antibodies [57]. Four patients had an advanced cSCC and one patient an advanced BCC. Two of the cSCC patients received pembrolizumab 2 mg/kg Q3W and the other two cSCC patients received nivolumab 3 mg/kg every 2 weeks (Q2W). One of the cSCC patients had a stereotactic radiation of a brain lesion while receiving pembrolizumab. PRs were observed in two cSCC patients who had been treated with pembrolizumab and nivolumab, respectively. Stable disease (SD) was observed in all remaining cSCC patients. PFS with pembrolizumab was reported to be ≥4 months and ≥7 months for the two patients and between 6 and at least 7 months for the nivolumab group. No median overall survival (OS), 1-year survival rates or serious AEs were reported. One patient receiving nivolumab died suddenly after 6 months most likely due to arrhythmia; however, the authors did not report whether his death was treatment-related.
Goldman et al. described the case of a kidney transplant recipient who developed multiple cSCC and metastases. Treatment with nivolumab 3 mg/kg led to a PR and a PFS of at least 18 months; however, the patient developed symptoms of an acute kidney injury and allograft rejection, which eventually resulted in the removal of the transplant [58]. The patient described by Oliveira et al. was diagnosed with lymph node and lung metastases from cSCC. Nivolumab also led to a PR, which lasted for at least 12 months [59]. Interestingly, a bone pseudo-progression was observed in several thoracic vertebrae by 18F-FDG PET/CT. No AEs ≥ grade 3 were reported.
Fujimura et al. reported the case of a patient with unresectable recurrent cSCC of the scalp with meningeal invasion and cervical lymph node metastases [60]. The patient was pretreated with cetuximab and cisplatin or 5-fluorouracil combination therapy and finally received nivolumab 240 mg Q2W, which led to a complete response (CR) with no signs of recurrence after 1 year at the time of the publication. No AEs were reported.
Oro-Ayude et al. described the case of a metastatic cSCC patient who was pretreated with cisplatin, cervical radiation and methotrexate [61]. He received nivolumab 3 mg/kg Q2W and achieved a CR ten months after the first dose. No AEs ≥ grade 3 were reported.
Two other publications summarized the efficacy of nivolumab and pembrolizumab for advanced cSCC. However, the authors did not distinguish clearly between both treatment regimens when reporting the results. Beasley et al. evaluated the efficacy of nivolumab and pembrolizumab for the treatment of unresectable cSCC in a retrospective study (n = 18) [62]. Seventeen patients received nivolumab 3 mg/kg Q2W or every 4 weeks (Q4W) in case a CR or PR were achieved with adverse effects such as fatigue; the remaining patient received pembrolizumab (2 mg/kg) Q3W. Four patients had a CR (22%) and 10 patients a PR (56%), resulting in an objective response rate (ORR) of 78%. Three patients showed SD and one patient progressive disease (PD). The median duration of response (DoR) was 12 months; median PFS and OS as well as 1-year survival rates and AEs ≥ grade 3 were not reported. Another case series from Blum et al. described three cSCC patients who received nivolumab (3 mg/kg) Q2W (n = 2) or 200 mg nivolumab Q2W (n = 1) [63]. All patients had a PR, and no AEs ≥ grade 3 were observed. Median PFS and OS as well as 1-year survival rates were not reported.

3.2.2. Pembrolizumab

In the prospective phase II study published by Ferrarotto et al., the efficacy of pembrolizumab (200 mg Q3W) in rare unresectable or metastatic cancers including cSCC (NCT02721732) was investigated [64]. Eleven patients with advanced cSCC were enrolled. PR was observed in four patients (36%), SD in one patient (9%) and PD in five patients (45%) within 27 weeks after initiation of the study. One patient had not been evaluated at the time of the publication. No AEs ≥ grade 3 were observed, and no median PFS and OS were reported.
The open-label, single arm, prospective phase II study KEYNOTE-629 (NCT03284424) investigated the efficacy of pembrolizumab (200 mg Q3W) in two cohorts of locally advanced and metastatic or recurrent cSCC. Grob et al. present the data of the first interim analysis of the cohort of recurrent or metastatic cSCC patients [65]. In total, 105 patients received at least one dose of pembrolizumab. CR was observed in 4 patients (3.8%), PR in 32 patients (30.5%), SD in 31 patients (29.5%) with 19 patients lasting for at least 12 weeks. Two patients were not evaluable and 8 patients were not assessed. Six patients (5.7%) developed treatment-related AEs of grade 3–5 and one patient died due to cranial nerve neuropathy which was considered treatment-related. In total, 28 patients (26.7%) interrupted and 13 patients (12.4%) discontinued the therapy due to AEs.
An open-label, prospective, single group, phase II study (NCT02964559) investigated pembrolizumab (200 mg Q3W) for up to 2 years in 11 patients with advanced cSCC [66]. CR was observed in two patients (18%) and PR in four patients (36%), resulting in an ORR of 54%. One patient (9%) had an SD and four patients (36%) a PD. The authors reported a 6-month PFS of 72% for evaluable patients and 50% of the patients that responded had a durable response of 18 months or greater at the time of data cut-off. Three AEs ≥ grade 3 were documented (hepatitis and pneumonitis).
The CARSKIN trial (NCT02883556), an open-label, single group, prospective phase II study, evaluated pembrolizumab (200 mg Q3W) in treatment-naive patients with advanced cSCC for up to 2 years [67]. Initially, 39 patients were enrolled in the study (primary cohort) and due to the promising interim results, 18 additional patients were recruited (expansion cohort). After 15 weeks, 3 CR (8%) and 13 PR (33%) were achieved in the primary cohort and 1 CR (8%) and 7 PR (39%) were observed in the expansion cohort. Survival data were only provided for the primary cohort. Median PFS was 6.7 months, median OS was 25.3 months and 1-year OS was 75.5%. Treatment-related AEs occurred in 71% of patients. Four patients (7%) had treatment-related AEs of grade ≥3 (colitis, diarrhea, cutaneous vasculitis and cholestasis).
Hermel et al. reported the results of an expanded access program (EAP) investigating pembrolizumab 2 mg/kg Q3W in 8 patients [68]. Half of the patients had a PR and no AEs ≥ grade 3 were observed. Other outcomes were not reported.
Lavaud et al. retrospectively evaluated the response of 4 patients with locally advanced cSCC [69]. They had received pembrolizumab 2 mg/kg Q3W until disease progression, unacceptable toxicity or the physician’s choice to discontinue treatment. Two patients achieved a CR and two patients PD. The median PFS was 14.4 months and the median OS was 15.6 months. No AEs were reported.
Several publications present the cases of patients with advanced cSCC who were successfully treated with pembrolizumab. Lipson et al. presented the case of a kidney-transplanted metastatic cSCC patient who was treated with pembrolizumab (2 mg/kg Q3W) [70,71]. The patient completely responded but developed an acute allograft rejection after 2 months of therapy with pembrolizumab and the kidney had subsequently to be removed. More than 4 years after the removal of the allograft, the patient was still tumor-free and underwent a second kidney transplantation and modified immunosuppression. At the time of the publication, the patient was relapse-free and the allograft had not been rejected for more than 10 months. In another patient with unresectable cSCC, a CR was observed with pembrolizumab 2 mg/kg Q3W [72]. The patient did not develop any AEs ≥ grade 3. Interestingly, the tumor harbored a mutation in the MLH1 gene, leading to an impaired DNA mismatch repair. Chang et al. described the case of a patient with unresectable cSCC [73]. The patient received pembrolizumab (2 mg/kg) Q3W, which led to a CR. No AEs ≥ grade 3 were reported in this publication; however, in the follow-up report of this case, the authors reported the occurrence of AEs ≥ grade 3, namely fatigue caused by endocrine hypofunction [74]. The duration of response of this patient was 21 months at the time of publication and still ongoing as described by Tran et al., who—in addition to this case—reported on the results of another five patients with advanced cSCC receiving pembrolizumab (2 mg/kg, Q3W, n = 4) or nivolumab (3 mg/m2, Q2W) [74]. One of the five patients had a CR (20%), three patients a PR and one patient receiving pembrolizumab a PD. PFS was 12 months for the patient treated with nivolumab and ranged from 3 to 10.5 months for pembrolizumab—median OS was not reported. One patient suffered from severe AEs; however, the authors did not mention the grade of severity. Deinlein et al. [75], Stevenson et al. [76], Degache et al. [77], Steineck et al. [78] and Ma et al. [79] reported the cases of six patients with advanced cSCC who received pembrolizumab (2 mg/kg, Q3W). The XP patient described by Deinlein et al. had a PR, which was still ongoing at the time of publication [75]. Similarly, a durable CR was also observed in the patient reported by Stevenson et al., which was still ongoing after 11 months of maintenance therapy. Both patients mentioned in Degache et al. had a PR [77]. Another XP patient successfully treated with pembrolizumab was presented by Steineck et al. [78]. The 7-year-old girl with metastatic cSCC received pembrolizumab and achieved a long-term PR. Ma et al. described the case of a metastatic cSCC patient successfully treated with pembrolizumab [79]. The patient completely responded and was disease-free for 17 months at the time of publication. No publications reported any AEs ≥ grade 3, and all patients were still alive at the time of publication.
Pembrolizumab also seems to be effective for the treatment of locally advanced cSCC as demonstrated by the following three case reports. Cristancho et al. reported the case of a patient with unresectable, locally advanced cSCC who received pembrolizumab 200 mg Q3W and achieved a CR for at least 1 year [80]. No AEs were observed. Delaitre et al. described the case of a patient with locally advanced cSCC on the scalp and BCC on the nose who received pembrolizumab 2 mg/kg Q3W [81]. A CR of the cSCC and BCC was observed after 11 cycles and 7 cycles, respectively. No AEs ≥ grade 3 were reported. Khaddour et al. reported the case of a patient with cutaneous T-cell lymphoma (CTCL) who received allogeneic hematopoietic stem cell transplantation (allo-HCT) and subsequently developed locally advanced cSCC and lymph node metastases [82]. Pembrolizumab 200 mg Q3W was administered, and the patient achieved a CR of cSCC and CTCL for at least 24 months. Pruritus and erythema caused by the CTCL significantly improved and graft-versus-host disease was not worsened. Only grade 1 AEs were reported (macular rash).

3.2.3. Cemiplimab

Migden et al. presented the results of a prospective open-label, multicenter phase I (NCT02383212) and a phase II trial (NCT02760498) evaluating cemiplimab for the treatment of advanced cSCC in 85 patients [83]. Twenty-six patients with locally advanced or metastatic cSCC were enrolled in the expansion cohorts of the phase I study and 59 patients with regional or distant cSCC metastases in the metastatic-disease cohort of the phase II study. The primary outcomes of the phase I study were the safety and AE profile, while the response rate assessed by independent central review was the primary outcome of the phase II study. The secondary outcomes in both studies included PFS, OS, DOR and toxic effects of cemiplimab. In both studies, cemiplimab (3mg/kg Q2W) was applied for up to 48 weeks (phase I) or 96 weeks (phase II) unless stopped due to disease progression or non-tolerable toxic effects.
In the phase I study, 13 patients (50%) had a PR, six patients showed a SD (23%) and three patients progressed (12%), resulting in an ORR of 50% (95% confidence interval (CI) 30–70). No CR was observed and three patients were not evaluable. Seven patients had a duration of response of more than 6 months. Six patients (23.1%) developed AEs of ≥ grade 3, but only two of them (7.7%) were considered to be treatment-related. During the phase I study, one patient died due to renal failure that was considered unrelated to the study treatment, and 3 patients died due to PD. Another patient who discontinued the treatment was lost to follow-up and died due to an unknown cause.
In the phase II study, the ORR was 47% (95% CI 34- 61). Four CR (7%) and 24 PR (41%) were achieved; nine patients (15%) had a SD and eleven patients (19%) a PD. Seven patients could not be evaluated. The median PFS and OS were not reached at the time of the data cut-off. The estimated probabilities of 1-year PFS and 1-year OS were 53% (95% CI 37–66) and 81% (95% CI 68–89), respectively. AEs of ≥ grade 3 were observed in 17 patients (29%) and were considered as treatment-related in five patients (8.5%). Altogether, eleven patients died during the study—eight patients due to the progression of the disease and three patients due to AEs. However, they were not classified as cemiplimab-related by the authors.
In a second cohort of the phase II study (NCT02760498), 78 patients with locally advanced cSCC were enrolled and received cemiplimab (3 mg/kg Q2W) [84]. The ORR by central review was 43.6% (95% CI 32.4–55.3) with 10 CR (13%) and 24 PR (31%). The median PFS and OS were not reached. Treatment-related AEs of ≥ grade 3 were observed in 10.3% of patients (8/78) and the death of one patient was considered as treatment-related. Recently, Rischin et al. published outcomes of another subgroup of this phase II study (NCT02760498) including 56 patients with metastatic cSCC who received fixed dose cemiplimab 350 mg Q3W [85]. The ORR was 41.1% (95% CI 28.1–55.0), and 3 CR (5%), 20 PR (36%), 8 SD (14%) and 14 PD (25%) were observed. The median PFS and OS had not been reached at the time of the publication. The estimated median PFS was 10.4 months, and the estimated 1-year OS was 76.1% (95% CI 56.9–87.6%). In total, 22 patients (39%) developed AEs ≥ grade 3, and 7 of them (12.5%) were considered treatment-related.
Escobar et al. described the case of a patient with both advanced cSCC and metastatic NSCLC who received cemiplimab 3 mg/kg Q2W and radiotherapy of the scalp and cervical region to control local bleeding [86]. The patient responded partially and the only remaining lesion was later excised. Secondary adrenal insufficiency was mentioned as AE, but the severity was not clearly reported. At the time of publication, there had been no tumor progression evident for 8 months.

3.3. Combined CTLA-4 and PD-1 Blockade

CTLA-4 and PD-1 blockade have been successfully combined in the past—e.g., for the treatment of advanced melanoma, achieving better results than the corresponding monotherapies [87,88,89]. However, dual ICB also increases the frequency of severe AEs [90].
Evidence for combined ICB in cSCC is sparse. Miller et al. reported the case of a kidney transplant recipient who developed metastatic cSCC 3 years after transplantation [91]. The patient had received a combination of ipilimumab and nivolumab after unsuccessful pretreatment with multiple other therapies. The precise dosage scheme was not indicated. The treatment led to a PR; however, the patient developed signs of an acute kidney injury, which led to the removal of the transplant less than 2 weeks after ICB initiation. The patient died 5 months after starting the immunotherapy during dialysis due to a sudden cardiac arrest that was not considered to be treatment-related and instead more likely to be a secondary complication of his long-term diabetes.
The case of another kidney transplant recipient was described by Trager et al. [92]. The patient developed metastatic cSCC after previous diagnoses of melanoma and multiple NMSC. After unsuccessful pretreatment with cetuximab and cisplatin, the patient was included in a single-arm, open-label, phase I study (NCT03816332) and received cemiplimab (350 mg Q3W) but showed disease progression and therapy was switched to combined ICB. Ipilimumab (3 mg/kg) and nivolumab (1 mg/kg) were administered and the patient partially responded. He developed a rash but otherwise tolerated the therapy well. No signs of allograft rejection were observed.

4. ICB in cSCC: The New Standard of Care?

The currently available evidence is still limited, but the results indicate that ICB also seems to be effective in cSCC. ICB generally achieves the highest response rates in tumors with high mutational burdens [55,93]. These tumors are more likely to express neoantigens that can be recognized by cytotoxic T lymphocytes (CTLs) as “foreign”, eventually leading to the lymphocyte-mediated killing of the tumor cells [94]. cSCC has one of the highest mutational burdens among all cancer entities and, therefore, might be a promising candidate for ICB [55,95,96]. However, predicting the success of ICB in cancer is challenging and even in cancer entities harboring an extremely high number of mutations, ICB fails in a subset of patients.
Furthermore, PD-L1 expression levels have been investigated in the past as potential biomarkers for predicting the outcome of ICB [97]. PD-L1-expressing tumors were associated with a better response in several trials investigating anti-PD-1 and anti-PD-L1 antibodies [98]. However, PD-L1 is not an ideal biomarker for predicting response to ICB. Determining tumor positivity by immunohistochemical staining is challenging as both tumor cells and infiltrating immune cells can express PD-L1, which seems to have a different impact on the prognosis [97,98]. Furthermore, expression can vary over time and is often heterogeneously distributed in the tumor tissue; thus, small biopsies may miss PD-L1 expressing cells [97,99]. These uncertainties have led to distinct cut-off values in clinical trials for defining PD-L1 positive tumors which are eligible for ICB, ranging from 1% up to 50% PD-L1 expressing tumor cells [100,101]. PD-L1 expression in cSCC has been evaluated in several retrospective analyses. Varki et al. observed that 26% of the investigated cSCC patients in their study had PD-L1-expressing tumors [102], and 20% of high-risk cSCC and 41% of metastatic cSCC evaluated by Slater and Googe had PD-L1-positive tumor cells [103]. Similarly, García-Díez et al. observed that 26% of non-metastatic cSCC and 50% of metastatic cSCC had at least 1% PD-L1- expressing cells, indicating that advanced cSCC are more likely to express PD-L1 [104]. These data are in line with a recent case series published by Wu et al. who detected PD-L1 expression in 85% of locally advanced and 100% of metastatic cSCC [105].
In addition to PD-L1 expression, the number of tumor-infiltrating immune cells is an important factor that influences response to ICB. Modulating T cells, which have already entered the tumor stroma, will more likely provoke an effective anti-tumor immune response. Immunologically “hot” tumors with a high number of CD3+ and CD8+ T cells at the tumor center are more susceptible to agents targeting CTLA-4, PD-L1 and PD-1 that modulate T cell function [106,107]. T cell infiltration in cSCC has not been extensively studied yet. However, Wu et al. detected tumor-infiltrating lymphocytes in all investigated samples, suggesting that cSCC may be a “hot” tumor suitable for successful ICB [105].
Based on the results of several phase II trials, the U.S. Food and Drug Administration (FDA) has recently approved cemiplimab and pembrolizumab for the treatment of locally advanced and metastatic cSCC [108,109]. In Europe, only cemiplimab is currently approved [110]. Cemiplimab and pembrolizumab appear to be the most evidence-based substances in this setting, as they were investigated in studies of better quality compared to the remaining publications. They achieved ORR ranging from 36 to 54% for pembrolizumab [65,66] and 41 to 50% for cemiplimab [83,84,85]. At the time of publication, the median PFS reported for pembrolizumab ranged from 6.7 to 6.9 months, and the median OS was 25.3 months in one study and was not reached in another trial [65,67]. Both median PFS and OS were not reached in the studies investigating cemiplimab [83,84,85]. Reported 1-year OS rates ranged from 60 to 76% with pembrolizumab [65,67] and from 76 to 93% with cemiplimab [83,84,85]. In addition to cemiplimab and pembrolizumab, other immune checkpoint-blocking antibodies also showed promising clinical results with objective and durable responses of at least 18 months [58]. However, most of the publications were selected case reports, being at high risk of publication bias. Furthermore, the quality of evidence is limited as ICB in cSCC patients has not been investigated in randomized controlled trials (RCTs) yet. Hence, the evidence for the use of ICB in cSCC is still limited compared to other entities such as melanoma. However, 27 trials investigating ICB in cSCC are currently ongoing (Table 2).
This lack of RCTs must be considered in future treatment guidelines which currently fall short of providing specific recommendation for ICB in advanced cSCC [111]. Nevertheless, due to the durable nature of the responses and the lack of treatment alternatives, ICB should receive a high grade of recommendation and should be discussed in the first treatment line in unresectable or metastatic disease.

5. ICB for Special cSCC Subgroups: Organ Transplant Recipients, Patients with Hematologic Malignancies, Xeroderma Pigmentosum, AK with Field Cancerization

In recent decades, the number of solid OTRs has been steadily rising. In 2018, 3595 transplantations were conducted in Germany, and there were 146,751 transplantations globally [112]. OTRs require immunosuppressing medication in order to prevent allograft rejection. However, constant immunosuppression not only dampens the immune response against the transplant but also impairs the response against precancerous cells. OTRs are at a 2- to 6-fold increased risk for developing tumors compared to the overall population [113] and a more than 100-fold increased risk for developing cSCC [114]. Unlike immunocompetent cSCC patients, OTRs more often develop multiple primary tumors as well as locally advanced and metastatic disease [115]. Treating advanced cSCC is challenging and the immune checkpoint-blocking agent cemiplimab can cause allograft rejection as it causes an activation of the immune system. However, patients may be willing to choose the lesser of two evils in certain circumstances. In the case of kidney transplant recipients, the loss of the transplanted organ will significantly diminish their quality of life, but it may be successfully compensated by hemodialysis. However, allograft rejection will certainly be life-threatening for patients who have received other organs such as heart and lung whose function cannot be permanently compensated by medical devices currently. On the other hand, effective alternative options for treating advanced cSCC are not available, highlighting the difficulties of choosing an appropriate therapy. Nevertheless, cemiplimab has been successfully used in OTRs in the past, as demonstrated by several case reports (Table 1). The results indicate that ICB is effective in these patients and the anti-tumor response does not seem to be compromised by previous immunosuppression or prednisone medication during ICB [58,71,92]. However, high-quality evidence is also lacking for this group of patients, and evidence on the efficacy is restricted to anecdotal reports. RCTs would also be desirable in this setting but most likely will not be conducted due to the limited number of affected patients. Thus, its use in OTRs remains controversial.
Nucleotide excision repair (NER) is a mechanism essentially required for the repair of bulky DNA alterations caused by UV light and other mutagens [116]. Mutations affecting the seven XP genes XPA to XPG or POLH which are part of the NER mechanism lead to XP, a rare genetic disorder that leads to the accumulation of mutations over time due to a permanently impaired NER. As a result, XP patients are at high risk for developing multiple melanoma and NMSC lesions including cSCC in sun-exposed body sites already at an early age [117]. No therapy for restoring NER function is available at the moment; thus, XP therapy focuses on the treatment of existing skin cancer lesions and their prevention. Surgical excision of multiple skin tumors and advanced disease may not always be the most suitable option. The case reports described above have demonstrated that ICB may be a suitable systemic therapy option for XP patients affected by advanced, unresectable cSCC [75,78]. In addition, other case reports which did not clearly distinguish between cSCC and other skin tumors and, therefore, were not included in the list above, underline the efficacy of ICB against melanoma and NMSC [118,119,120,121].
While ICB has been used for the treatment of cSCC, little is known of the efficacy against precancerous lesions such as AK. AK are keratinocytic lesions arising in chronically sun-damaged areas that eventually progress to invasive cSCC [3,122]. Orloff et al. presented the impact on NMSC and AK in a case series of three patients who received ICB for other indications [123]. One of the cases described in this series was a patient with metastatic melanoma and extended AK. After receiving two doses of ipilimumab followed by two doses of pembrolizumab, all AK lesions disappeared. The authors did not comment on the efficacy of ICB against the metastatic disease in this patient. Although this report suggests that ICB can clear AK lesions, other physicians (personal communication) and we could not observe such effects in our patients. Anyhow, ICB will hardly ever be used as a treatment against AK as several other efficient and more favorable options in terms of safety profile exist. Thus, AK may be cleared by ICB only as a side effect, if at all.
Recently, Leiter et al. reported the results of a retrospective analysis evaluating the efficacy of ICB in non-resectable melanoma, cSCC and Merkel cell carcinoma with and without concomitant hematological malignancies [124]. Seventy-five of the included patients had unresectable, advanced cSCC and received either nivolumab or pembrolizumab. Fifteen cSCC patients had a concomitant hematological malignancy, most of them chronic lymphatic leukemia (n = 8) and other types of non-Hodgkin lymphoma (n = 5). In this subgroup, one patient achieved a CR and three patients a PR, resulting in an ORR of 26.7%. The median PFS and OS were 4.0 months (95% CI 0.3 to 7.9) and 14.9 months (95% CI 0.1 to 31.2), respectively. In the subgroup of cSCC patients without hematological malignancies, the ORR was 33.8% with eight patients achieving a CR and twelve a PR. Here, the median PFS and OS were not reached at the time of publication. There were no statistically significant differences between both cSCC subgroups except for the PFS (p = 0.002). AEs were not reported in this publication.

6. Conclusions

Advanced cSCC is a major therapeutic challenge and still difficult to treat. In the past, several treatment variations have failed to demonstrate their anti-tumor efficacy. This has now at least partly changed. Although the evidence is still limited, ICB has achieved very promising results in this cancer entity, finally leading to the recent approval of the anti-PD-1 antibodies cemiplimab in Europe and the U.S. and pembrolizumab in the U.S. With these antibodies, we have important tools now to treat advanced cSCC also in difficult-to-treat patients. Promising results have also been observed in special patient groups such as OTRs and XP patients. Nevertheless, future high-quality RCTs will be required to underline the efficacy of ICB in this cancer entity.

Author Contributions

Conceptualization, A.W., T.S., C.B. and M.V.H.; methodology, A.W. and T.S.; validation, A.W., T.S., U.L., C.G., C.B. and M.V.H.; formal analysis, A.W. and T.S.; investigation, A.W., T.S., C.B. and M.V.H.; resources, C.B. and M.V.H.; data curation, A.W., T.S., U.L., C.G., C.B. and M.V.H.; writing—original draft preparation, A.W. and T.S.; writing—review and editing, U.L., C.G., C.B. and M.V.H.; visualization, A.W. and T.S.; supervision, U.L., C.G., C.B. and M.V.H.; project administration, C.B. and M.V.H. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

C.B. has been member of advisory boards for and/or has received speaker honoraria by Almirall Hermal, Bristol-Myers Squibb, Immunocore, Leo Pharma, Merck, MSD, Novartis, Pierre Fabre, Regeneron, Roche and Sanofi-Aventis. M.V.H. has been a member of advisory boards for Almirall Hermal, Sanofi-Aventis and received speaker honoraria by Galderma. C.G. reports personal fees from Amgen, grants and personal fees from BMS, personal fees from MSD, grants and personal fees from Novartis, personal fees from Philogen, personal fees from Pierre Fabre, grants and personal fees from Roche, grants and personal fees from Sanofi, Jansen outside the submitted work. All other authors report no conflicts of interest.

Abbreviations

α-MSHalpha-melanocyte-stimulating hormone
ACTHadrenocorticotropic hormone
Ad-MAGEA3adenovirus vaccine expressing melanoma-associated antigen 3
AEsadverse events
AKactinic keratoses
allo-HCTallogeneic hematopoietic stem cell transplantation
ASIPagouti signaling protein
BCCbasal cell carcinoma
BIDtwice daily
CIconfidence interval
CMcutaneous melanoma
CRcomplete response
cSCCcutaneous squamous cell carcinoma
CTCLcutaneous T cell lymphoma
CTLcytotoxic T lymphocyte
DCRdisease control rate
DoRduration of response
EAPexpanded access program
EGFRepidermal growth factor receptor
EMAEuropean Medicines Agency
FDAU.S. Food and Drug Administration
FGFfibroblast growth factor
GVHDgraft-versus-host disease
GyGray
HGFhepatocyte growth factor
HNSCChead and neck squamous cell carcinoma
i.m.intramuscular
i.t.intratumoral
i.v.intravenous
ICBimmune checkpoint blockade
laSCClocally advanced cSCC
MC1Rmelanocortin 1 receptor
MG1-MAGEA3MG1 Maraba oncolytic virus expressing melanoma-associated antigen 3
mSCCmetastatic cSCC
NERnucleotide excision repair
NMSCnon-melanoma skin cancer
NSCLCnon-small cell lung cancer
ORRobjective response rate
OSoverall survival
OTRorgan transplant recipient
PDprogressive disease
PFSprogression-free survival
PRpartial response
POMCproopiomelanocortin
PYsperson-years
Q2Wevery 2 weeks
Q3Wevery 3 weeks
Q4Wevery 4 weeks
Q6Wevery 6 weeks
QDdaily
QoLquality of life
QWevery week
RCTrandomized-controlled trial
RFSrecurrence free survival
rhIL-7-hyFcrecombinant human interleukin-7 and hybrid Fc fusion protein
RP1genetically modified herpes simplex virus 1
RRresponse rate
SCFstem cell factor
SDstable disease
T-VECtalimogene laherparepvec
XPxeroderma pigmentosum

References

  1. Lomas, A.; Leonardi-Bee, J.; Bath-Hextall, F. A systematic review of worldwide incidence of nonmelanoma skin cancer. Br. J. Dermatol. 2012, 166, 1069–1080. [Google Scholar] [CrossRef] [PubMed]
  2. Sanchez-Danes, A.; Blanpain, C. Deciphering the cells of origin of squamous cell carcinomas. Nat. Rev. Cancer 2018, 18, 549–561. [Google Scholar] [CrossRef] [PubMed]
  3. Criscione, V.D.; Weinstock, M.A.; Naylor, M.F.; Luque, C.; Eide, M.J.; Bingham, S.F.; Department of Veteran Affairs Topical Tretinoin Chemoprevention Trial Group. Actinic keratoses: Natural history and risk of malignant transformation in the Veterans Affairs Topical Tretinoin Chemoprevention Trial. Cancer 2009, 115, 2523–2530. [Google Scholar] [CrossRef] [PubMed]
  4. Werner, R.N.; Sammain, A.; Erdmann, R.; Hartmann, V.; Stockfleth, E.; Nast, A. The natural history of actinic keratosis: A systematic review. Br. J. Dermatol. 2013, 169, 502–518. [Google Scholar] [CrossRef] [PubMed]
  5. Cerio, R.; Dirschka, T.; Dreno, B.; Figueras Nart, I.; Lear, J.T.; Pellacani, G.; Peris, K.; de Casas, A.R. Actinic Keratosis, a Chronic, Progressive Disease: Understanding Clinical Gaps to Optimise Patient Management. Acta Derm. Venereol. 2017, 97, 997–998. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Green, A.C.; Olsen, C.M. Cutaneous squamous cell carcinoma: An epidemiological review. Br. J. Dermatol. 2017, 177, 373–381. [Google Scholar] [CrossRef]
  7. Muzic, J.G.; Schmitt, A.R.; Wright, A.C.; Alniemi, D.T.; Zubair, A.S.; Olazagasti Lourido, J.M.; Sosa Seda, I.M.; Weaver, A.L.; Baum, C.L. Incidence and Trends of Basal Cell Carcinoma and Cutaneous Squamous Cell Carcinoma: A Population-Based Study in Olmsted County, Minnesota, 2000 to 2010. Mayo Clin. Proc. 2017, 92, 890–898. [Google Scholar] [CrossRef] [PubMed]
  8. Stang, A.; Khil, L.; Kajuter, H.; Pandeya, N.; Schmults, C.D.; Ruiz, E.S.; Karia, P.S.; Green, A.C. Incidence and mortality for cutaneous squamous cell carcinoma: Comparison across three continents. J. Eur. Acad. Dermatol. Venereol. 2019, 33, 6–10. [Google Scholar] [CrossRef] [Green Version]
  9. Xiang, F.; Lucas, R.; Hales, S.; Neale, R. Incidence of nonmelanoma skin cancer in relation to ambient UV radiation in white populations, 1978–2012: Empirical relationships. JAMA Dermatol. 2014, 150, 1063–1071. [Google Scholar] [CrossRef] [Green Version]
  10. Leiter, U.; Garbe, C. Epidemiology of melanoma and nonmelanoma skin cancer—The role of sunlight. Adv. Exp. Med. Biol. 2008, 624, 89–103. [Google Scholar] [CrossRef]
  11. Subramaniam, P.; Olsen, C.M.; Thompson, B.S.; Whiteman, D.C.; Neale, R.E.; Sun, Q.S.; Health Study, I. Anatomical Distributions of Basal Cell Carcinoma and Squamous Cell Carcinoma in a Population-Based Study in Queensland, Australia. JAMA Dermatol. 2017, 153, 175–182. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Mittal, A.; Colegio, O.R. Skin Cancers in Organ Transplant Recipients. Am. J. Transpl. 2017, 17, 2509–2530. [Google Scholar] [CrossRef] [PubMed]
  13. Silverberg, M.J.; Leyden, W.; Warton, E.M.; Quesenberry, C.P., Jr.; Engels, E.A.; Asgari, M.M. HIV infection status, immunodeficiency, and the incidence of non-melanoma skin cancer. J. Natl. Cancer Inst. 2013, 105, 350–360. [Google Scholar] [CrossRef] [PubMed]
  14. Velez, N.F.; Karia, P.S.; Vartanov, A.R.; Davids, M.S.; Brown, J.R.; Schmults, C.D. Association of advanced leukemic stage and skin cancer tumor stage with poor skin cancer outcomes in patients with chronic lymphocytic leukemia. JAMA Dermatol. 2014, 150, 280–287. [Google Scholar] [CrossRef]
  15. Brewer, J.D.; Shanafelt, T.D.; Khezri, F.; Sosa Seda, I.M.; Zubair, A.S.; Baum, C.L.; Arpey, C.J.; Cerhan, J.R.; Call, T.G.; Roenigk, R.K.; et al. Increased incidence and recurrence rates of nonmelanoma skin cancer in patients with non-Hodgkin lymphoma: A Rochester Epidemiology Project population-based study in Minnesota. J. Am. Acad. Dermatol. 2015, 72, 302–309. [Google Scholar] [CrossRef] [Green Version]
  16. Slominski, A.T.; Zmijewski, M.A.; Plonka, P.M.; Szaflarski, J.P.; Paus, R. How UV Light Touches the Brain and Endocrine System through Skin, and Why. Endocrinology 2018, 159, 1992–2007. [Google Scholar] [CrossRef] [Green Version]
  17. Wikonkal, N.M.; Brash, D.E. Ultraviolet radiation induced signature mutations in photocarcinogenesis. J. Investig. Dermatol. Symp. Proc. 1999, 4, 6–10. [Google Scholar] [CrossRef] [Green Version]
  18. Halliday, G.M.; Bestak, R.; Yuen, K.S.; Cavanagh, L.L.; Barnetson, R.S. UVA-induced immunosuppression. Mutat. Res. 1998, 422, 139–145. [Google Scholar] [CrossRef]
  19. Schierbeck, J.; Vestergaard, T.; Bygum, A. Skin Cancer Associated Genodermatoses: A Literature Review. Acta Derm. Venereol. 2019, 99, 360–369. [Google Scholar] [CrossRef] [Green Version]
  20. Mohan, S.V.; Chang, J.; Li, S.; Henry, A.S.; Wood, D.J.; Chang, A.L. Increased Risk of Cutaneous Squamous Cell Carcinoma after Vismodegib Therapy for Basal Cell Carcinoma. JAMA Dermatol. 2016, 152, 527–532. [Google Scholar] [CrossRef] [Green Version]
  21. Peng, L.; Wang, Y.; Hong, Y.; Ye, X.; Shi, P.; Zhang, J.; Zhao, Q. Incidence and relative risk of cutaneous squamous cell carcinoma with single-agent BRAF inhibitor and dual BRAF/MEK inhibitors in cancer patients: A meta-analysis. Oncotarget 2017, 8, 83280–83291. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. European Medicines Agency (EMA). EMA Review of Picato Concludes Medicine’s Risks Outweigh Its Benefits. 2020. Available online: https://www.ema.europa.eu/en/news/ema-review-picato-concludes-medicines-risks-outweigh-its-benefits (accessed on 19 October 2020).
  23. Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM). Rote-Hand-Brief zu Picato® (Ingenolmebutat): Vorsicht bei der Behandlung von Patienten mit Hautkrebsanamnese. Available online: https://www.bfarm.de/SharedDocs/Risikoinformationen/Pharmakovigilanz/DE/RHB/2019/rhb-picato.pdf?__blob=publicationFile&v=7 (accessed on 26 October 2020).
  24. Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM). Rote-Hand-Brief zu Picato® (Ingenolmebutat)—Ruhen der Zulassungen aufgrund des Risikos von malignen Hautveränderungen. Available online: https://www.bfarm.de/SharedDocs/Risikoinformationen/Pharmakovigilanz/DE/RHB/2020/rhb-picato.pdf;jsessionid=767355ADF2B76F472CEC011BA27627F5.1_cid319?__blob=publicationFile&v=1 (accessed on 26 October 2020).
  25. Que, S.K.T.; Zwald, F.O.; Schmults, C.D. Cutaneous squamous cell carcinoma: Management of advanced and high-stage tumors. J. Am. Acad. Dermatol. 2018, 78, 249–261. [Google Scholar] [CrossRef] [PubMed]
  26. Edwards, M.J.; Hirsch, R.M.; Broadwater, J.R.; Netscher, D.T.; Ames, F.C. Squamous cell carcinoma arising in previously burned or irradiated skin. Arch. Surg. 1989, 124, 115–117. [Google Scholar] [CrossRef] [PubMed]
  27. Kauvar, A.N.; Arpey, C.J.; Hruza, G.; Olbricht, S.M.; Bennett, R.; Mahmoud, B.H. Consensus for Nonmelanoma Skin Cancer Treatment, Part II: Squamous Cell Carcinoma, Including a Cost Analysis of Treatment Methods. Dermatol. Surg. 2015, 41, 1214–1240. [Google Scholar] [CrossRef]
  28. Gellrich, F.F.; Huning, S.; Beissert, S.; Eigentler, T.; Stockfleth, E.; Gutzmer, R.; Meier, F. Medical treatment of advanced cutaneous squamous-cell carcinoma. J. Eur. Acad. Dermatol. Venereol. 2019, 33, 38–43. [Google Scholar] [CrossRef] [Green Version]
  29. Brunner, M.; Veness, M.J.; Ch’ng, S.; Elliott, M.; Clark, J.R. Distant metastases from cutaneous squamous cell carcinoma—Analysis of AJCC stage IV. Head Neck 2013, 35, 72–75. [Google Scholar] [CrossRef]
  30. Chapalain, M.; Baroudjian, B.; Dupont, A.; Lhote, R.; Lambert, J.; Bagot, M.; Lebbe, C.; Basset-Seguin, N. Stage IV cutaneous squamous cell carcinoma (cSCC): Treatment outcomes in a series of 42 patients. J. Eur. Acad. Dermatol. Venereol. 2019, 34, 1202–1209. [Google Scholar] [CrossRef]
  31. Pasquali, S.; Hadjinicolaou, A.V.; Chiarion Sileni, V.; Rossi, C.R.; Mocellin, S. Systemic treatments for metastatic cutaneous melanoma. Cochrane Database Syst. Rev. 2018, 2, CD011123. [Google Scholar] [CrossRef]
  32. Giroux Leprieur, E.; Dumenil, C.; Julie, C.; Giraud, V.; Dumoulin, J.; Labrune, S.; Chinet, T. Immunotherapy revolutionises non-small-cell lung cancer therapy: Results, perspectives and new challenges. Eur. J. Cancer 2017, 78, 16–23. [Google Scholar] [CrossRef]
  33. Cramer, J.D.; Burtness, B.; Ferris, R.L. Immunotherapy for head and neck cancer: Recent advances and future directions. Oral Oncol. 2019, 99, 104460. [Google Scholar] [CrossRef]
  34. Eckhart, L.; Lippens, S.; Tschachler, E.; Declercq, W. Cell death by cornification. Biochim. Biophys. Acta 2013, 1833, 3471–3480. [Google Scholar] [CrossRef] [PubMed]
  35. Shain, A.H.; Bastian, B.C. From melanocytes to melanomas. Nat. Rev. Cancer 2016, 16, 345–358. [Google Scholar] [CrossRef] [PubMed]
  36. Jimbow, K.; Roth, S.I.; Fitzpatrick, T.B.; Szabo, G. Mitotic activity in non-neoplastic melanocytes in vivo as determined by histochemical, autoradiographic, and electron microscope studies. J. Cell Biol. 1975, 66, 663–670. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Simon, J.D.; Peles, D.; Wakamatsu, K.; Ito, S. Current challenges in understanding melanogenesis: Bridging chemistry, biological control, morphology, and function. Pigment Cell Melanoma Res. 2009, 22, 563–579. [Google Scholar] [CrossRef] [PubMed]
  38. D’Mello, S.A.; Finlay, G.J.; Baguley, B.C.; Askarian-Amiri, M.E. Signaling Pathways in Melanogenesis. Int. J. Mol. Sci. 2016, 17, 1144. [Google Scholar] [CrossRef] [Green Version]
  39. Haass, N.K.; Herlyn, M. Normal human melanocyte homeostasis as a paradigm for understanding melanoma. J. Investig. Dermatol. Symp. Proc. 2005, 10, 153–163. [Google Scholar] [CrossRef] [Green Version]
  40. Lin, J.Y.; Fisher, D.E. Melanocyte biology and skin pigmentation. Nature 2007, 445, 843–850. [Google Scholar] [CrossRef]
  41. Slominski, A.; Tobin, D.J.; Shibahara, S.; Wortsman, J. Melanin pigmentation in mammalian skin and its hormonal regulation. Physiol. Rev. 2004, 84, 1155–1228. [Google Scholar] [CrossRef]
  42. Videira, I.F.; Moura, D.F.; Magina, S. Mechanisms regulating melanogenesis. An. Bras. Dermatol. 2013, 88, 76–83. [Google Scholar] [CrossRef] [Green Version]
  43. Scherer, D.; Kumar, R. Genetics of pigmentation in skin cancer—A review. Mutat. Res. 2010, 705, 141–153. [Google Scholar] [CrossRef]
  44. Slominski, A.T.; Zmijewski, M.A.; Zbytek, B.; Tobin, D.J.; Theoharides, T.C.; Rivier, J. Key role of CRF in the skin stress response system. Endocr. Rev. 2013, 34, 827–884. [Google Scholar] [CrossRef] [PubMed]
  45. Slominski, A.; Wortsman, J.; Luger, T.; Paus, R.; Solomon, S. Corticotropin releasing hormone and proopiomelanocortin involvement in the cutaneous response to stress. Physiol. Rev. 2000, 80, 979–1020. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Slominski, A.; Wortsman, J. Neuroendocrinology of the skin. Endocr. Rev. 2000, 21, 457–487. [Google Scholar] [CrossRef] [PubMed]
  47. Nasti, T.H.; Timares, L. MC1R, eumelanin and pheomelanin: Their role in determining the susceptibility to skin cancer. Photochem. Photobiol. 2015, 91, 188–200. [Google Scholar] [CrossRef] [Green Version]
  48. Wong, R.C.; Ellis, C.N. Physiologic skin changes in pregnancy. J. Am. Acad. Dermatol. 1984, 10, 929–940. [Google Scholar] [CrossRef]
  49. Hu, M.S.; Borrelli, M.R.; Hong, W.X.; Malhotra, S.; Cheung, A.T.M.; Ransom, R.C.; Rennert, R.C.; Morrison, S.D.; Lorenz, H.P.; Longaker, M.T. Embryonic skin development and repair. Organogenesis 2018, 14, 46–63. [Google Scholar] [CrossRef] [Green Version]
  50. Aiello, N.M.; Stanger, B.Z. Echoes of the embryo: Using the developmental biology toolkit to study cancer. Dis. Model Mech. 2016, 9, 105–114. [Google Scholar] [CrossRef] [Green Version]
  51. Hohenauer, T.; Berking, C.; Schmidt, A.; Haferkamp, S.; Senft, D.; Kammerbauer, C.; Fraschka, S.; Graf, S.A.; Irmler, M.; Beckers, J.; et al. The neural crest transcription factor Brn3a is expressed in melanoma and required for cell cycle progression and survival. EMBO Mol. Med. 2013, 5, 919–934. [Google Scholar] [CrossRef]
  52. Heppt, M.V.; Wang, J.X.; Hristova, D.M.; Wei, Z.; Li, L.; Evans, B.; Beqiri, M.; Zaman, S.; Zhang, J.; Irmler, M.; et al. MSX1-Induced Neural Crest-Like Reprogramming Promotes Melanoma Progression. J. Investig. Dermatol. 2018, 138, 141–149. [Google Scholar] [CrossRef] [Green Version]
  53. Leiter, U.; Eigentler, T.; Garbe, C. Epidemiology of skin cancer. Adv. Exp. Med. Biol. 2014, 810, 120–140. [Google Scholar] [CrossRef]
  54. Schadendorf, D.; van Akkooi, A.C.J.; Berking, C.; Griewank, K.G.; Gutzmer, R.; Hauschild, A.; Stang, A.; Roesch, A.; Ugurel, S. Melanoma. Lancet 2018, 392, 971–984. [Google Scholar] [CrossRef]
  55. Yarchoan, M.; Hopkins, A.; Jaffee, E.M. Tumor Mutational Burden and Response Rate to PD-1 Inhibition. N. Engl. J. Med. 2017, 377, 2500–2501. [Google Scholar] [CrossRef] [PubMed]
  56. Day, F.; Kumar, M.; Fenton, L.; Gedye, C. Durable Response of Metastatic Squamous Cell Carcinoma of the Skin to Ipilimumab Immunotherapy. J. Immunother. 2017, 40, 36–38. [Google Scholar] [CrossRef] [PubMed]
  57. Borradori, L.; Sutton, B.; Shayesteh, P.; Daniels, G.A. Rescue therapy with anti-programmed cell death protein 1 inhibitors of advanced cutaneous squamous cell carcinoma and basosquamous carcinoma: Preliminary experience in five cases. Br. J. Dermatol. 2016, 175, 1382–1386. [Google Scholar] [CrossRef]
  58. Goldman, J.W.; Abdalla, B.; Mendenhall, M.A.; Sisk, A.; Hunt, J.; Danovitch, G.M.; Lum, E.L. PD 1 checkpoint inhibition in solid organ transplants: 2 sides of a coin—Case report. BMC Nephrol. 2018, 19, 210. [Google Scholar] [CrossRef]
  59. Oliveira, L.J.C.; Gongora, A.B.L.; Barbosa, F.G.; Dos Anjos, C.H.; Munhoz, R.R. Atypical response with bone pseudoprogression in a patient receiving nivolumab for advanced cutaneous squamous cell carcinoma. J. Immunother. Cancer 2018, 6, 130. [Google Scholar] [CrossRef]
  60. Fujimura, T.; Kambayashi, Y.; Tono, H.; Lyu, C.; Ohuchi, K.; Hashimoto, A.; Aiba, S. Successful treatment of unresectable recurrent cutaneous squamous cell carcinoma of the scalp with meningeal invasion with nivolumab monotherapy. Dermatol. Ther. 2020, e13672. [Google Scholar] [CrossRef]
  61. Oro-Ayude, M.; Suh-Oh, H.J.; Sacristan-Santos, V.; Vazquez-Bartolome, P.; Florez, A. Nivolumab for Metastatic Cutaneous Squamous Cell Carcinoma. Case Rep. Dermatol. 2020, 12, 37–41. [Google Scholar] [CrossRef]
  62. Beasley, G.M.; Kurtz, J.; Vandeusen, J.; Howard, J.H.; Terando, A.; Agnese, D.; Liebner, D.; Jeter, J.; Olencki, T. Immune Checkpoint Inhibitor Therapy as a Novel and Effective Therapy for Aggressive Cutaneous Squamous-cell Carcinoma. Clin. Skin Cancer 2017, 05. [Google Scholar] [CrossRef]
  63. Blum, V.; Muller, B.; Hofer, S.; Pardo, E.; Zeidler, K.; Diebold, J.; Strobel, K.; Brand, C.; Aebi, S.; Gautschi, O. Nivolumab for recurrent cutaneous squamous cell carcinoma: Three cases. Eur. J. Dermatol. 2018, 28, 78–81. [Google Scholar] [CrossRef]
  64. Ferrarotto, R.; Glisson, B.; Blumenschein, G.; Hong, D.; Piha-Paul, S.; Jain, D.; Alshawa, A.; Painter, J.; Hess, K.; Colen, R.; et al. Efficacy of pembrolizumab in patients with cutaneous aquamous cell carcinoma. J. Immunother. Cancer 2017, 5. [Google Scholar] [CrossRef] [Green Version]
  65. Grob, J.J.; Gonzalez, R.; Basset-Seguin, N.; Vornicova, O.; Schachter, J.; Joshi, A.; Meyer, N.; Grange, F.; Piulats, J.M.; Bauman, J.R.; et al. Pembrolizumab Monotherapy for Recurrent or Metastatic Cutaneous Squamous Cell Carcinoma: A Single-Arm Phase II Trial (KEYNOTE-629). J. Clin. Oncol. 2020, 38, 2916–2925. [Google Scholar] [CrossRef] [PubMed]
  66. Yushak, M.L.; Lawson, D.H.; Goings, M.; Mckellar, M.; Maynard, N.; Woodruff, K.S.; Gorgoglione, C.; McBrien, S.; Delman, K.A.; Lowe, M.C.; et al. Phase II trial of pembrolizumab (MK-3475) in metastatic cutaneous squamous cell carcinoma: An updated analysis. J. Clin. Oncol. 2019, 37, e21015. [Google Scholar] [CrossRef]
  67. Maubec, E.; Boubaya, M.; Petrow, P.; Beylot-Barry, M.; Basset-Seguin, N.; Deschamps, L.; Grob, J.J.; Dreno, B.; Scheer-Senyarich, I.; Bloch-Queyrat, C.; et al. Phase II Study of Pembrolizumab As First-Line, Single-Drug Therapy for Patients With Unresectable Cutaneous Squamous Cell Carcinomas. J. Clin. Oncol. 2020, 38, 3051–3061. [Google Scholar] [CrossRef] [PubMed]
  68. Hermel, D.J.; Ragab, O.M.; Higgins, S.; Wysong, A.; Kim In, G. PD-1 inhibition in cutaneous squamous cell carcinoma (cSCC). J. Clin. Oncol. 2018, 36, e15100. [Google Scholar] [CrossRef]
  69. Lavaud, J.; Blom, A.; Longvert, C.; Fort, M.; Funck-Brentano, E.; Saiag, P. Pembrolizumab and concurrent hypo-fractionated radiotherapy for advanced non-resectable cutaneous squamous cell carcinoma. Eur. J. Dermatol. 2019, 29, 636–640. [Google Scholar] [CrossRef] [Green Version]
  70. Lipson, E.J.; Bagnasco, S.M.; Moore, J., Jr.; Jang, S.; Patel, M.J.; Zachary, A.A.; Pardoll, D.M.; Taube, J.M.; Drake, C.G. Tumor Regression and Allograft Rejection after Administration of Anti-PD-1. N. Engl. J. Med. 2016, 374, 896–898. [Google Scholar] [CrossRef] [Green Version]
  71. Lipson, E.J.; Naqvi, F.F.; Loss, M.J.; Schollenberger, M.D.; Pardoll, D.M.; Moore, J., Jr.; Brennan, D.C. Kidney retransplantation after anti-programmed cell death-1 (PD-1)-related allograft rejection. Am. J. Transpl. 2020, 20, 2264–2268. [Google Scholar] [CrossRef]
  72. Assam, J.H.; Powell, S.; Spanos, W.C. Unresectable cutaneous squamous cell carcinoma of the forehead with MLH1 mutation showing dramatic response to Programmed Cell Death Protein 1 Inhibitor Therapy. Clin. Skin. Cancer 2016, 1, 26–29. [Google Scholar] [CrossRef] [Green Version]
  73. Chang, A.L.; Kim, J.; Luciano, R.; Sullivan-Chang, L.; Colevas, A.D. A Case Report of Unresectable Cutaneous Squamous Cell Carcinoma Responsive to Pembrolizumab, a Programmed Cell Death Protein 1 Inhibitor. JAMA Dermatol. 2016, 152, 106–108. [Google Scholar] [CrossRef] [Green Version]
  74. Tran, D.C.; Colevas, A.D.; Chang, A.L.S. Follow-up on programmed cell death 1 inhibitor for cutaneous squamous cell carcinoma. JAMA Dermatol. 2017, 153, 92–94. [Google Scholar] [CrossRef] [PubMed]
  75. Deinlein, T.; Lax, S.F.; Schwarz, T.; Giuffrida, R.; Schmid-Zalaudek, K.; Zalaudek, I. Rapid response of metastatic cutaneous squamous cell carcinoma to pembrolizumab in a patient with xeroderma pigmentosum: Case report and review of the literature. Eur. J. Cancer 2017, 83, 99–102. [Google Scholar] [CrossRef] [PubMed]
  76. Stevenson, M.L.; Wang, C.Q.F.; Abikhair, M.; Roudiani, N.; Felsen, D.; Krueger, J.G.; Pavlick, A.C.; Carucci, J.A. Expression of programmed cell death ligand in cutaneous squamous cell carcinoma and treatment of locally advanced disease with pembrolizumab. JAMA Dermatol. 2017, 153, 299–303. [Google Scholar] [CrossRef] [PubMed]
  77. Degache, E.; Crochet, J.; Simon, N.; Tardieu, M.; Trabelsi, S.; Moncourier, M.; Templier, I.; Foroni, L.; Lemoigne, A.; Pinel, N.; et al. Major response to pembrolizumab in two patients with locally advanced cutaneous squamous cell carcinoma. J. Eur. Acad. Dermatol. Venereol. 2018, 32, e257–e258. [Google Scholar] [CrossRef] [PubMed]
  78. Steineck, A.; Krumm, N.; Sarthy, J.F.; Pritchard, C.C.; Chapman, T.; Stacey, A.W.; Vitanza, N.A.; Cole, B. Response to Pembrolizumab in a Patient with Xeroderma Pigmentosum and Advanced Squamous Cell Carcinoma. JCO Precis. Oncol. 2019, 3. [Google Scholar] [CrossRef]
  79. Ma, W.L.; Chou, C.H.; Chen, J.P.; Kuo, S.H. Efficacy of a programmed death-1 checkpoint inhibitor in a case of cutaneous squamous cell carcinoma harboring mutations of TP53 and BRCA2. Dermatol. Ther. 2020, e14035. [Google Scholar] [CrossRef]
  80. Cristancho, C.; Riano, I.; Guareras-Paredes, D.; Park, R.; Seetharaman, K. Complete Resolution of a Large, Locally-advanced Cutaneous Squamous Cell Carcinoma with the Immune-modulating PD-1 Inhibitor Pembrolizumab. Cureus 2020, 12, e8072. [Google Scholar] [CrossRef]
  81. Delaitre, L.; Martins-Hericher, J.; Truchot, E.; Denis, D.; Prophette, B.; Maillard, H.; Beneton-Benhard, N. Regression of cutaneous basal cell and squamous cell carcinoma under pembrolizumab. Ann. Dermatol. Venereol. 2020, 147, 279–284. [Google Scholar] [CrossRef]
  82. Khaddour, K.; Musiek, A.; Cornelius, L.A.; Dehdashti, F.; Westervelt, P.; Fields, R.; Ansstas, G. Rapid and sustained response to immune checkpoint inhibition in cutaneous squamous cell carcinoma after allogenic hematopoietic cell transplant for sezary syndrome. J. Immunother. Cancer 2019, 7, 338. [Google Scholar] [CrossRef]
  83. Migden, M.R.; Rischin, D.; Schmults, C.D.; Guminski, A.; Hauschild, A.; Lewis, K.D.; Chung, C.H.; Hernandez-Aya, L.; Lim, A.M.; Chang, A.L.S.; et al. PD-1 Blockade with Cemiplimab in Advanced Cutaneous Squamous-Cell Carcinoma. N. Engl. J. Med. 2018, 379, 341–351. [Google Scholar] [CrossRef] [Green Version]
  84. Migden, M.R.; Khushalani, N.I.; Chang, A.L.S.; Lewis, K.D.; Schmults, C.D.; Hernandez-Aya, L.; Meier, F.; Schadendorf, D.; Guminski, A.; Hauschild, A.; et al. Cemiplimab in locally advanced cutaneous squamous cell carcinoma: Results from an open-label, phase 2, single-arm trial. Lancet Oncol. 2020, 21, 294–305. [Google Scholar] [CrossRef]
  85. Rischin, D.; Migden, M.R.; Lim, A.M.; Schmults, C.D.; Khushalani, N.I.; Hughes, B.G.M.; Schadendorf, D.; Dunn, L.A.; Hernandez-Aya, L.; Chang, A.L.S.; et al. Phase 2 study of cemiplimab in patients with metastatic cutaneous squamous cell carcinoma: Primary analysis of fixed-dosing, long-term outcome of weight-based dosing. J. Immunother. Cancer 2020, 8. [Google Scholar] [CrossRef] [PubMed]
  86. Escobar, G.F.; Granel-Brocard, F.; Schmutz, J.L.; Cervantes, P.; Ben Mahmoud, S.; Bursztejn, A.C. Simultaneous response of cutaneous and lung squamous cell carcinoma with cemiplimab. Dermatol. Ther. 2020, e13951. [Google Scholar] [CrossRef] [PubMed]
  87. Larkin, J.; Chiarion-Sileni, V.; Gonzalez, R.; Grob, J.J.; Rutkowski, P.; Lao, C.D.; Cowey, C.L.; Schadendorf, D.; Wagstaff, J.; Dummer, R.; et al. Five-Year Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma. N. Engl. J. Med. 2019, 381, 1535–1546. [Google Scholar] [CrossRef] [Green Version]
  88. Larkin, J.; Chiarion-Sileni, V.; Gonzalez, R.; Grob, J.J.; Cowey, C.L.; Lao, C.D.; Schadendorf, D.; Dummer, R.; Smylie, M.; Rutkowski, P.; et al. Combined Nivolumab and Ipilimumab or Monotherapy in Untreated Melanoma. N. Engl. J. Med. 2015, 373, 23–34. [Google Scholar] [CrossRef] [Green Version]
  89. Postow, M.A.; Chesney, J.; Pavlick, A.C.; Robert, C.; Grossmann, K.; McDermott, D.; Linette, G.P.; Meyer, N.; Giguere, J.K.; Agarwala, S.S.; et al. Nivolumab and ipilimumab versus ipilimumab in untreated melanoma. N. Engl. J. Med. 2015, 372, 2006–2017. [Google Scholar] [CrossRef] [Green Version]
  90. Hassel, J.C.; Heinzerling, L.; Aberle, J.; Bahr, O.; Eigentler, T.K.; Grimm, M.O.; Grunwald, V.; Leipe, J.; Reinmuth, N.; Tietze, J.K.; et al. Combined immune checkpoint blockade (anti-PD-1/anti-CTLA-4): Evaluation and management of adverse drug reactions. Cancer Treat. Rev. 2017, 57, 36–49. [Google Scholar] [CrossRef]
  91. Miller, D.M.; Faulkner-Jones, B.E.; Stone, J.R.; Drews, R.E. Complete pathologic response of metastatic cutaneous squamous cell carcinoma and allograft rejection after treatment with combination immune checkpoint blockade. JAAD Case Rep. 2017, 3, 412–415. [Google Scholar] [CrossRef] [Green Version]
  92. Trager, M.H.; Coley, S.M.; Dube, G.; Khan, S.; Ingham, M.; Samie, F.H.; Geskin, L.J.; McDonnell, D.; Brouder, D.; Saenger, Y.; et al. Combination checkpoint blockade for metastatic cutaneous malignancies in kidney transplant recipients. J. Immunother. Cancer 2020, 8, e000908. [Google Scholar] [CrossRef]
  93. Rizvi, N.A.; Hellmann, M.D.; Snyder, A.; Kvistborg, P.; Makarov, V.; Havel, J.J.; Lee, W.; Yuan, J.; Wong, P.; Ho, T.S.; et al. Cancer immunology. Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer. Science 2015, 348, 124–128. [Google Scholar] [CrossRef] [Green Version]
  94. Schumacher, T.N.; Schreiber, R.D. Neoantigens in cancer immunotherapy. Science 2015, 348, 69–74. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  95. Pickering, C.R.; Zhou, J.H.; Lee, J.J.; Drummond, J.A.; Peng, S.A.; Saade, R.E.; Tsai, K.Y.; Curry, J.L.; Tetzlaff, M.T.; Lai, S.Y.; et al. Mutational landscape of aggressive cutaneous squamous cell carcinoma. Clin. Cancer Res. 2014, 20, 6582–6592. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  96. Chalmers, Z.R.; Connelly, C.F.; Fabrizio, D.; Gay, L.; Ali, S.M.; Ennis, R.; Schrock, A.; Campbell, B.; Shlien, A.; Chmielecki, J.; et al. Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden. Genome Med. 2017, 9, 34. [Google Scholar] [CrossRef] [PubMed]
  97. Topalian, S.L.; Taube, J.M.; Anders, R.A.; Pardoll, D.M. Mechanism-driven biomarkers to guide immune checkpoint blockade in cancer therapy. Nat. Rev. Cancer 2016, 16, 275–287. [Google Scholar] [CrossRef]
  98. Meng, X.; Huang, Z.; Teng, F.; Xing, L.; Yu, J. Predictive biomarkers in PD-1/PD-L1 checkpoint blockade immunotherapy. Cancer Treat. Rev. 2015, 41, 868–876. [Google Scholar] [CrossRef]
  99. Topalian, S.L.; Hodi, F.S.; Brahmer, J.R.; Gettinger, S.N.; Smith, D.C.; McDermott, D.F.; Powderly, J.D.; Carvajal, R.D.; Sosman, J.A.; Atkins, M.B.; et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N. Engl. J. Med. 2012, 366, 2443–2454. [Google Scholar] [CrossRef]
  100. Brahmer, J.; Reckamp, K.L.; Baas, P.; Crino, L.; Eberhardt, W.E.; Poddubskaya, E.; Antonia, S.; Pluzanski, A.; Vokes, E.E.; Holgado, E.; et al. Nivolumab versus Docetaxel in Advanced Squamous-Cell Non-Small-Cell Lung Cancer. N. Engl. J. Med. 2015, 373, 123–135. [Google Scholar] [CrossRef] [Green Version]
  101. Garon, E.B.; Rizvi, N.A.; Hui, R.; Leighl, N.; Balmanoukian, A.S.; Eder, J.P.; Patnaik, A.; Aggarwal, C.; Gubens, M.; Horn, L.; et al. Pembrolizumab for the treatment of non-small-cell lung cancer. N. Engl. J. Med. 2015, 372, 2018–2028. [Google Scholar] [CrossRef]
  102. Varki, V.; Ioffe, O.B.; Bentzen, S.M.; Heath, J.; Cellini, A.; Feliciano, J.; Zandberg, D.P. PD-L1, B7-H3, and PD-1 expression in immunocompetent vs. immunosuppressed patients with cutaneous squamous cell carcinoma. Cancer Immunol. Immunother. 2018, 67, 805–814. [Google Scholar] [CrossRef]
  103. Slater, N.A.; Googe, P.B. PD-L1 expression in cutaneous squamous cell carcinoma correlates with risk of metastasis. J. Cutan. Pathol. 2016, 43, 663–670. [Google Scholar] [CrossRef]
  104. Garcia-Diez, I.; Hernandez-Ruiz, E.; Andrades, E.; Gimeno, J.; Ferrandiz-Pulido, C.; Yebenes, M.; Garcia-Patos, V.; Pujol, R.M.; Hernandez-Munoz, I.; Toll, A. PD-L1 Expression is Increased in Metastasizing Squamous Cell Carcinomas and Their Metastases. Am. J. Dermatopathol. 2018, 40, 647–654. [Google Scholar] [CrossRef] [PubMed]
  105. Wu, S.; Slater, N.A.; Sayed, C.J.; Googe, P.B. PD-L1 and LAG-3 expression in advanced cutaneous squamous cell carcinomas. J. Cutan Pathol. 2020, 47, 882–887. [Google Scholar] [CrossRef] [PubMed]
  106. Galon, J.; Bruni, D. Approaches to treat immune hot, altered and cold tumours with combination immunotherapies. Nat. Rev. Drug Discov. 2019, 18, 197–218. [Google Scholar] [CrossRef] [PubMed]
  107. Gajewski, T.F.; Corrales, L.; Williams, J.; Horton, B.; Sivan, A.; Spranger, S. Cancer Immunotherapy Targets Based on Understanding the T Cell-Inflamed Versus Non-T Cell-Inflamed Tumor Microenvironment. Adv. Exp. Med. Biol. 2017, 1036, 19–31. [Google Scholar] [CrossRef]
  108. Markham, A.; Duggan, S. Cemiplimab: First Global Approval. Drugs 2018, 78, 1841–1846. [Google Scholar] [CrossRef]
  109. U.S. Food and Drug Administration. FDA Approves Pembrolizumab for Cutaneous Squamous Cell Carcinoma; 2020. Available online: https://www.fda.gov/drugs/drug-approvals-and-databases/fda-approves-pembrolizumab-cutaneous-squamous-cell-carcinoma (accessed on 22 October 2020).
  110. European Medicines Agency (EMA). Libtayo (Cemiplimab). Available online: https://www.ema.europa.eu/en/medicines/human/EPAR/libtayo (accessed on 28 October 2020).
  111. Heppt, M.V.; Steeb, T.; Berking, C.; Nast, A. Comparison of guidelines for the management of patients with high-risk and advanced cutaneous squamous cell carcinoma—A systematic review. J. Eur. Acad. Dermatol. Venereol. 2019, 33, 25–32. [Google Scholar] [CrossRef] [Green Version]
  112. Global Observatory on Donation and Transplantation. Summary—Total Number of Organ Transplant Recipients in Germany and Global. 2018. Available online: http://www.transplant-observatory.org/summary/ (accessed on 9 June 2020).
  113. Madeleine, M.M.; Patel, N.S.; Plasmeijer, E.I.; Engels, E.A.; Bouwes Bavinck, J.N.; Toland, A.E.; Green, A.C.; The Keratinocyte Carcinoma Consortium Immunosuppression Working Group. Epidemiology of keratinocyte carcinomas after organ transplantation. Br. J. Dermatol. 2017, 177, 1208–1216. [Google Scholar] [CrossRef] [Green Version]
  114. Harwood, C.A.; Toland, A.E.; Proby, C.M.; Euvrard, S.; Hofbauer, G.F.L.; Tommasino, M.; Bouwes Bavinck, J.N.; KeraCon, C. The pathogenesis of cutaneous squamous cell carcinoma in organ transplant recipients. Br. J. Dermatol. 2017, 177, 1217–1224. [Google Scholar] [CrossRef] [Green Version]
  115. Leitlinienprogramm Onkologie; Deutsche Krebsgesellschaft; Deutsche Krebshilfe; AWMF. S3-Leitlinie Aktinische Keratose und Plattenepithelkarzinom der Haut, Langversion 1.1. Available online: https://www.leitlinienprogrammonkologie.de/leitlinien/aktinische-keratosen-und-plattenepithelkarzinom-der-haut/ (accessed on 5 June 2020).
  116. Marteijn, J.A.; Lans, H.; Vermeulen, W.; Hoeijmakers, J.H. Understanding nucleotide excision repair and its roles in cancer and ageing. Nat. Rev. Mol. Cell Biol. 2014, 15, 465–481. [Google Scholar] [CrossRef]
  117. Lehmann, J.; Seebode, C.; Martens, M.C.; Emmert, S. Xeroderma Pigmentosum—Facts and Perspectives. Anticancer Res. 2018, 38, 1159–1164. [Google Scholar] [CrossRef]
  118. Hauschild, A.; Eichstaedt, J.; Mobus, L.; Kahler, K.; Weichenthal, M.; Schwarz, T.; Weidinger, S. Regression of melanoma metastases and multiple non-melanoma skin cancers in xeroderma pigmentosum by the PD1-antibody pembrolizumab. Eur. J. Cancer 2017, 77, 84–87. [Google Scholar] [CrossRef] [PubMed]
  119. Salomon, G.; Maza, A.; Boulinguez, S.; Paul, C.; Lamant, L.; Tournier, E.; Mazereeuw-Hautier, J.; Meyer, N. Efficacy of anti-programmed cell death-1 immunotherapy for skin carcinomas and melanoma metastases in a patient with xeroderma pigmentosum. Br. J. Dermatol. 2018, 178, 1199–1203. [Google Scholar] [CrossRef] [PubMed]
  120. Chambon, F.; Osdoit, S.; Bagny, K.; Moro, A.; Nguyen, J.; Reguerre, Y. Dramatic response to nivolumab in xeroderma pigmentosum skin tumor. Pediatr. Blood Cancer 2018, 65. [Google Scholar] [CrossRef] [PubMed]
  121. Kraemer, K.H.; Tamura, D.; Khan, S.G. Pembrolizumab treatment of a patient with xeroderma pigmentosum with disseminated melanoma and multiple nonmelanoma skin cancers. Br. J. Dermatol. 2018, 178, 1009. [Google Scholar] [CrossRef] [PubMed]
  122. Cantisani, C.; Paolino, G.; Melis, M.; Faina, V.; Romaniello, F.; Didona, D.; Cardone, M.; Calvieri, S. Actinic Keratosis Pathogenesis Update and New Patents. Recent Pat. Inflamm. Allergy Drug Discov. 2016, 10, 40–48. [Google Scholar] [CrossRef]
  123. Orloff, M.M.; Dasgeb, B.; Mastrangelo, M.J.; Koblenzer, P.; Kemp, D.; Weight, R.M.; Javed, A.; Sharpe-Mills, E.; Sato, T. Resolution of pre-cancerous and non-melanoma skin cancers after immune checkpoint inhibitor treatments. J. Clin. Oncol. 2016, 34, e14540. [Google Scholar] [CrossRef]
  124. Leiter, U.; Loquai, C.; Reinhardt, L.; Rafei-Shamsabadi, D.; Gutzmer, R.; Kaehler, K.; Heinzerling, L.; Hassel, J.C.; Glutsch, V.; Sirokay, J.; et al. Immune checkpoint inhibition therapy for advanced skin cancer in patients with concomitant hematological malignancy: A retrospective multicenter DeCOG study of 84 patients. J. Immunother. Cancer 2020, 8, e000897. [Google Scholar] [CrossRef]
Table
Table 1. Immune checkpoint blockade in cutaneous squamous cell carcinoma (cSCC) patients.
Table 1. Immune checkpoint blockade in cutaneous squamous cell carcinoma (cSCC) patients.
Author, Year [Reference]DesignnInterventionORRPRCRPFS (Months)OS (Months)1-Year OSAEs ≥Grade 3
Day 2017 [56]Case report1Ipi *1/11/10/1≥8--0
Borradori 2016 [57]Case series2Pem 2 mg/kg1/21/20/2≥4, ≥7--0
3Nivo 3 mg/kg1/21/20/26 to ≥7--0
Beasley 2017 [62]Case series17Nivo 3 mg/kg14/1810/184/18---3/18
(fatigue, haemolytic anemia, colitis)
1Pem 2 mg/kg
Blum 2018 [63]Case series2Nivo 3 mg/kg3/33/30/3---0
1Nivo 200 mg fix
Goldman 2018 [58]Case report1 (OTR)Nivo 3 mg/kg1/11/10/1≥18--allograft rejection
Fujimura 2020 [60]Case report1Nivo 240 mg fix1/10/11/1----
Oliveira 2018 [59]Case report1Nivo 3 mg/kg1/11/10/1≥12--0
Oro-Ayude 2020 [61]Case report1Nivo 3 mg/kg1/10/11/1---0
Assam 2016 [72]Case report1Pem 2 mg/kg1/10/11/1---0
Chang 2016 [73]Case report1Pem 2 mg/kg1/10/11/1---unclear
Cristancho 2020 [80]Case report1Pem 200 mg fix1/10/11/1---0
Degache 2018 [77]Case series2Pem 2 mg/kg2/22/20/2---0
Deinlein 2017 [75]Case report1 (XP patient)Pem 2 mg/kg1/11/10/1---0
Delaitre 2020 [81]Case report1Pem 2 mg/kg1/10/11/1---0
Ferrarotto 2017 [64]
NCT02721732		Phase II11Pem 200 mg fix4/114/110/11---0
Grob 2020 [65]
KEYNOTE-629
NCT03284424		Phase II105Pem 200 mg fix36/10532/1054/1056.9n.r.60.3%6 (5.7%, grade 3–5)
Hermel 2018 [68]EAP8Pem 2 mg/kg4/84/80/8---0
Khaddour 2019 [82]Case report1 (allo-HCT)Pem 200 mg fix1/10/11/1≥ 24--0
Lavaud 2019 [69]Retrospective analysis/case series4Pem 2 mg/kg2/40/42/414.415.6-0
Lipson 2016/2020 [70,71]Case report1 (OTR)Pem 2 mg/kg1/10/11/1---allograft rejection
Maubec 2020 [67]
CARSKIN trial
NCT02883556		Phase II39 (primary cohort)Pem 200 mg fix16/3913/393/396.725.375.5%4 (7%)
18 (expansion cohort)Pem 200 mg fix8/187/181/18----
Ma 2020 [79]Case report1Pem 2 mg/kg1/10/11/1≥17--0
Steineck 2019 [78]Case report1 (XP patient)Pem1/11/10/1≥18---
Stevenson 2017 [76]Case report1Pem 2 mg/kg1/10/11/1---0
Tran 2017 [74]Case series4Pem 2 mg/kg3/42/41/43 to 10.5--0
1Nivo 3 mg/m21/11/10/112--0
Yushak 2019 [66]
NCT02964559		Phase II11Pem 200 mg fix6/114/112/11≥6--3 AEs reported
Escobar 2020 [86]Case report1Cem 3 mg/kg Q2W1/11/10/1≥8--unclear
Migden 2018/2020, Rischin 2020 [83,84,85]
NCT02383212 (phase I)
NCT02760498 (phase II)		Phase I (la)26Cem 3 mg/kg13/2613/260/26---6/26
Phase II (m)5928/5924/594/59n.r.n.r.81%17/59
Phase II (la)7834/7824/7810/78n.r.n.r.93%8/78
Phase II (m)56Cem 350 mg fix23/5620/563/56n.r.n.r.76.1%7/56
Miller 2017 [91]Case report1 (OTR)Ipi and nivo *1/11/10/1---allograft rejection
Trager 2020 [92]Case report1 (OTR)Ipi 3 mg/kg and nivo 1 mg/kg1/11/10/1≥9--unclear
Note: - = not reported; EAP = expanded access program; ORR = overall response rate; PR = partial response; CR = complete response; PFS = progression-free survival; OS = overall survival; n.r. = not reached; AEs = adverse events; OTR = organ transplant recipient; XP = xeroderma pigmentosum patient; allo-HCT = allogeneic hematopoietic cell transplantation; la = locally advanced; m = metastatic; ipi = ipilimumab; pem = pembrolizumab; nivo = nivolumab; cem = cemiplimab; AE = adverse events; * no dosage reported in the studies.
Table
Table 2. Ongoing trials investigating immune checkpoint blockade (ICB) in advanced cSCC.
Table 2. Ongoing trials investigating immune checkpoint blockade (ICB) in advanced cSCC.
Study IDStudy DesignStartEnd *Sample Size [n]InterventionPrimary OutcomesSecondary OutcomesFunding
NCT03901573Multicenter, open-label, phase IbDec 2019May 202424Atezolizumab i.v.+ efineptakin alfa (hIL-7-hyFc) i.m.
Dose escalation		Safety and tolerabilityORR, DCR, DOR, PFS, OSNeoImmuneTech
Immune Oncology Network
Multicenter, open-label, two armed, phase IIa60
(A = 24,
B = 36)		Atezolizumab i.v.+ efineptakin alfa (rhIL-7-hyFc) i.m.
A: ICB-refractory cSCC
B: ICB-naïve cSCC
Dose expansion
NCT03108131Single-center, single-arm, open-label, phase IIApr 2017Jul 202060Atezolizumab i.v. Q2W + cobimetinib p.o. QD on days 1–12, 1 cycle = 28 days, until disease progression or unacceptable toxicityORRPFSM.D. Anderson Cancer Center
National Cancer Institute (NCI)
NCT03944941Multicenter, open-label, randomized, two-armed, phase IIMay 2019Dec 202359A: Avelumab i.v. on days 1 and 15, up to 24 cycles (1 cycle = 28 days), until disease progression or unacceptable toxicity; patients with avelumab failure will crossover to arm B
B: Avelumab + cetuximab: and avelumab i.v. on days 1 and 15 + cetuximab i.v. on days 1, 8, 15, and 22, up to 24 cycles until disease progression or unacceptable toxicity		PFSORR, clinical benefit rate, OS, AEsAlliance for Clinical Trials in Oncology
National Cancer Institute (NCI)
AliCe Trial
EudraCT: 2018-001708-12 		Multicenter, open-label, single-arm, phase II un-clearun-clear52Avelumab i.v. + cetuximab i.v., intervals and dosage not reportedORRPFS, DOR, OS, AEs, QoLAlcedis GmbH
UNSCARRed trial
NCT03737721		Single-center, single-arm, open-label, phase IIApr 2019Jun 202320Avelumab i.v. Q2W, first dose 14 days prior to radiotherapy, then 63–66 Gy radiation over 30 daily fractions + avelumab i.v. Q2W for 4 cycles ORRPFS, clinical and pathological response rate, AEsAHS Cancer Control Alberta
EMD Serono
Alberta Cancer Foundation
NCT03889912Multicenter, single-arm, open-label, phase IApr 2019Feb 202236Cemiplimab i.t. QW for 12 weeks neoadjuvant, then surgical excisionAEsORR, CR rate, pathological response rate, drug concentration over time, anti-drug antibodiesRegeneron Pharmaceuticals
Sanofi
NCT04154943Multicenter, single-arm, open-label, phase IIMar 2020Dec 202476Cemiplimab i.v. Q3WPathologic CR rateMajor pathologic response, ORR, event-free survival, DFS, OS, AEs, incidence of deathsRegeneron Pharmaceuticals
Sanofi
NCT03969004
(EudraCT: 2019-000566-38)		Randomized, multicenter, two-armed, double-blind, phase IIIJun 2019Feb 2026412Surgery and radiation therapy followed by
A: Cemiplimab i.v.
B: Placebo i.v.
Intervals and dosage not reported		DFSOS, freedom from locoregional and distant recurrence, cumulative occurance of second primary cSCC, AEs, incidence of deathsRegeneron Pharmaceuticals
Sanofi
NCT04242173Single-center, single-arm, open-label, phase IIJan 2020Jan 202327Cemiplimab i.v., intervals and dosage not reportedORRPFS, OSRegeneron Pharmaceuticals
Sanofi
CERPASS trial
NCT04050436		Randomized, multicenter, two-armed, open-label, phase IIOct 2019Mar 2024240A: Cemiplimab i.v. Q3W
B: Cemiplimab i.v. Q3W+ RP1 i.t. Q3W		ORRDOR, PFS, CR rate, OS, AEs, response injected vs. non-injected lesionsReplimune Inc.
Regeneron Pharmaceuticals
CONTRAC trial
NCT04339062		Non-randomized, single-center, open-label, phase IJul 2020Jul 202212
A: allo-HCT
B: kidney trans-plant reci-pients		A: Cemiplimab i.v. Q3W
B: Cemiplimab i.v. Q3W
+ everolimus/sirolimus 7–10 days prior to cemiplimab start, then QD
+ prednisone 40 mg p.o. 1 day prior to cemiplimab start, then QD at tapering doses		Dose-limiting toxicity (A: GVHD, B: allograft rejection)PFS, OS, ORR, therapeutic response rate, secondary infection rate, Dana-Farber Cancer Institute
Regeneron Pharmaceuticals
NCT02760498
(EudraCT: 2016-000105-36)		Multicenter, open-label, phase IIApr 2016Dec 2025433Cemiplimab i.v.
A: mSCC, Q2W
B: laSCC, Q2W
C: mSCC, Q3W
D: mSCC or laSCC, Q4W
E: mSCC or laSCC, Q3W		ORRDoR, PFS, OS, CR rate, QoL, AEs, pharmacokinetics, correlation PD-L1 expression and ORR/DoR/PFSRegeneron Pharmaceuticals
NCT04428671Single-center, open-label, phase IMay 2020Oct 203020Cemiplimab i.v. Q3W neoadjuvant for up to 3 cycles prior to surgery, then cemiplimab i.v. Q3W adjuvant, starting within 2–6 weeks after surgery or radiation therapy, up to 18 cyclesPathologic RRTime to local and systemic recurrence, OS, RFSEmory University
NCT04315701Multicenter, open-label, phase IIJun 2020Jan 202334Cemiplimab i.v. Q3W up to 3 cycles neoadjuvant, then surgery within 6 weeks after last dosePathologic PRPathologic CR rate, ORR, PFS, AEsM.D. Anderson Cancer Center
National Cancer Institute (NCI)
NCT03684785Multicenter, open-label, phase IbDec 2018Jun 2023130Cavrotolimod i.t. twice (dosage and intervals not reported), then with pembrolizumab 2 mg/kg i.v. Q3W
Dose escalation		AEsFinding recommended dose of cavrotolimod for phase II trial
ORR, biomarkers		Exicure, Inc.
Phase IICemiplimab 350 mg i.v. Q3W
+ cavrotolimod i.t.
Dose expansion
NCT04305795Open-label, phase I/IISep 2020Jun 202454Cemiplimab 350 mg i.v., up to 24 months
+ ASP-1929 (EGFR antibody-dye conjugate for photoimmunotherapy light treatment)		AEs, ORR OS, PFS, DORRakuten Medical, Inc.
NCT03816332Multicenter, single-arm, open-label, phase I Feb 2019May 202116
kidney trans-plant reci-pients 		Tacrolimus p.o. BID + prednisone p.o. QD, within 28 days: Nivolumab i.v. Q4W, up to 24 cycles until disease progression or unacceptable toxicity.
Patients with PD at 16 weeks: Nivolumab i.v. + ipilimumab i.v. Q3W + tacrolimus p.o. BID + prednisone p.o. QD, up to 4 cycles until disease progression or unacceptable toxicity. Starting 6 weeks later, patients receive nivolumab i.v. Q4W, up to 21 cycles until disease progression or unacceptable toxicity.		CR, PR and SD rate, patients without allograft lossORR, allograft rejection rate, DOR (CR and PR), PFS, OSNational Cancer Institute (NCI)
CA209-9JC trial
NCT03834233		Single-center, open-label, phase IISep 2019Dec 202224Nivolumab 3 mg/kg i.v. Q2W until disease progression or up to 12 monthsORRAEs, PFSInstituto do Cancer do Estado de São Paulo
NCT04204837Multicenter, open-label, phase IIMar 2017Dec 202331Nivolumab 240 mg i.v. Q2W until disease progression, unacceptable toxicity or up to 2 yearsORRDCR, DOR, PFS, OSSalzburger Landeskliniken
Bristol-Myers Squibb
NCT02978625Multicenter, open-label, phase IISep 2017Jun 202168T-VEC i.t. on day 1, if no response:
Nivolumab i.v. Q3W (first cycle), then Q2W until disease progression, unacceptable toxicity or up to 1 year		RR to T-VEC alone, ORR to T-VEC + nivolumabDurable RR, RR of injected and non-injected lesions, PFS, OS, AEsNational Cancer Institute (NCI)
Pelican trial
NCT03773744		Open-label, phase IJan 2020Dec 202140A: Cyclophosphamide 300mg/m2 3 days prior to Ad-MAGEA3 fixed dose i.m. (day 1), then one of 3 dose levels of MG1-MAGEA3 i.v. (day 15 and 18) + pembrolizumab 200 mg i.v., starting in week 6 or on day 1 (depending on cohort; intervals not reported)
B: Ad-MAGEA3 fixed dose i.m. followed by pembrolizumab i.v. (day 1), then MG1-MAGEA3 i.v. (day 15) and i.t. on day 22, 29, and 36; MG1-MAGEA3 booster injections i.t. Q3W beginning at day 43 (=week 6)		AEs, maximum tolerated and feasible dose of Ad/MG-MAGEA3ORR, DCR, PFS, DORTurnstone Biologics, Corp.
KEYNOTE-629
NCT03284424
(EudraCT: 2017-000594-37)		Multicenter, two-armed, open-label, phase IIOct 2017Jun 2022150Pembrolizumab 200 mg i.v. Q3W up to 2 years
A: recurrent or mSCC
B: laSCC		ORRDOR, DCR, PFS, OS, AEs, discontinuations due to AEsMerck Sharp & Dohme Corp.
KEYNOTE-630
NCT03833167
(EudraCT: 2018-001974-76)		Randomized, multicenter, blinded, controlled, phase IIIApr 2019Sep 2027570Adjuvant setting
A: Pembrolizumab 400 mg i.v. Q6W, up to 9 cycles; if 9 cycles completed: Up to 18 additional cycles in open-label design
B: Placebo i.v. Q6W, up to 9 cycles; if disease recurrence: Up to 18 cycles of pembrolizumab in open-label design		RFSOS, QoL, AEs, discontinuations due to AEsMerck Sharp & Dohme Corp.
NCT02964559Single-center, open-label, phase IIJan 2017Feb 202211Pembrolizumab i.v. Q3W until disease progression or unacceptable toxicityRROS, PFSEmory University
Merck Sharp & Dohme Corp.
CARSKIN trial
NCT02883556
(EudraCT: 2016-002076-28)		Single-center, open-label, phase IIMar 2017Oct 202157Pembrolizumab 200 mg i.v. Q3W until disease progression or unacceptable toxicity, or up to 24 monthsRRAEs, RR in PD-L1 positive patients, DCR, OS, PFS, DOR, duration of control, time to progressionAssistance Publique - Hôpitaux de Paris
NCT02721732Single-center, open-label, phase IIAug 2016Aug 2020225Pembrolizumab i.v. Q3W until disease progression or unacceptable toxicity, or up to 24 months; responding patients may continue up to 12 additional monthsNon-progression rate, AEsORR, clinical benefit (CR, PR or SD), DOR, PFS, OS, ECOG performance status, temperature, pulse, body weight, respiratory rate, blood pressureM.D. Anderson Cancer Center
National Cancer Institute (NCI)
NCT04234113Multicenter, open-label, phase IJun 2019Mar 202296A: SO-C101 (IL-15 agonist)
B: SO-C101 + Pembrolizumab i.v.
unclear dosing and intervals		Dose-limiting toxicity, AEs, laboratory test abnormalities, ECOG performance statusORR, best overall response, DOR, clinical benefit rate, PFS, anti-drug antibodies to SO-C101Sotio a.s.
*: estimated; Abbreviations: Ad-MAGEA3: Adenovirus vaccine expressing Melanoma-associated antigen 3, AEs: adverse events, allo-HCT: allogeneic hematopoietic stem cell transplant, BID: twice daily, CR: complete response, cSCC: cutaneous squamous cell carcinoma, DCR: disease control rate, DOR: Duration of response, GVHD: Graft-versus-Host-disease, Gy: Gray, i.m.: intramuscular, i.t.: intratumoral, i.v.: intravenous, laSCC: locally advanced cSCC, MG1-MAGEA3: MG1 Maraba oncolytic virus expressing Melanoma-associated antigen 3, mSCC: metastatic cSCC, ORR: objective response rate, OS: Overall survival, PFS: Progression-free survival, p.o.: per os, PR: partial response, QoL: quality of life, QD: daily, QW: every week, Q2W: every 2 weeks, Q3W: every 3 weeks, Q4W: every 4 weeks, Q6W: every 6 weeks, RFS: recurrence free survival, RR: response rate, rhIL-7-hyFc: recombinant human interleukin-7 and hybrid Fc fusion protein, RP1: genetically modified herpes simplex virus 1; T-VEC: Talimogene laherparepvec.
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Wessely, A.; Steeb, T.; Leiter, U.; Garbe, C.; Berking, C.; Heppt, M.V. Immune Checkpoint Blockade in Advanced Cutaneous Squamous Cell Carcinoma: What Do We Currently Know in 2020? Int. J. Mol. Sci. 2020, 21, 9300. https://doi.org/10.3390/ijms21239300

AMA Style

Wessely A, Steeb T, Leiter U, Garbe C, Berking C, Heppt MV. Immune Checkpoint Blockade in Advanced Cutaneous Squamous Cell Carcinoma: What Do We Currently Know in 2020? International Journal of Molecular Sciences. 2020; 21(23):9300. https://doi.org/10.3390/ijms21239300

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Wessely, Anja, Theresa Steeb, Ulrike Leiter, Claus Garbe, Carola Berking, and Markus Vincent Heppt. 2020. "Immune Checkpoint Blockade in Advanced Cutaneous Squamous Cell Carcinoma: What Do We Currently Know in 2020?" International Journal of Molecular Sciences 21, no. 23: 9300. https://doi.org/10.3390/ijms21239300

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Wessely, A., Steeb, T., Leiter, U., Garbe, C., Berking, C., & Heppt, M. V. (2020). Immune Checkpoint Blockade in Advanced Cutaneous Squamous Cell Carcinoma: What Do We Currently Know in 2020? International Journal of Molecular Sciences, 21(23), 9300. https://doi.org/10.3390/ijms21239300

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