1. Introduction
Head and neck squamous cell carcinoma (HNSCC) is an aggressive, life-threatening malignancy worldwide and is the sixth leading cause of death in Taiwan [
1]. The location of HNSCC includes the nasal cavity, oral cavity, oropharynx, hypopharynx, and larynx. Tobacco smoking, alcohol consumption, and betel nut chewing are well-known risk factors for HNSCC; however, not all causes of HNSCC are related to these behaviors. Human papillomavirus (HPV) is a nonenveloped double-stranded DNA virus that infects and replicates in skin and mucous membranes. The carcinogenicity of HPV was recognized as being associated with cervical cancer by Professor Haral zur Hausen in the 1970s. HPV infection was also identified in 1983 in patients with oral squamous cell carcinoma [
2]. To date, more than 220 HPV types have been classified. Recently, growing evidence has confirmed an association between HPV and HNSCC, and the incidence of HPV-positive HNSCC has significantly increased, especially in the oropharynx [
3,
4,
5].
p16, also called cyclin-dependent kinase inhibitor 2A (CDKN2A), is a cyclin-dependent kinase (CDK) inhibitor that arrests the cell cycle in the G1 stage. Its gene product inhibits CDK4/6 binding with cyclin D, resulting in phosphorylation of retinoblastoma (Rb). The dephosphorylated Rb subsequently entraps nuclear transcription factor E2F and blocks the ability to bind to other transcription factors to inhibit G1/S phase progression and prevent cell proliferation. In HPV+ HNSCC, the loss of viral regulatory E2 gene contributes to increased E7 oncoprotein, which binds phosphorylated Rb, and results in its dissociation from E2F [
6]. The latter, in turn, upregulates the transcription of cell-growth- and proliferation-related genes, including cyclin A, cyclin E, and p53 [
7]. This dysfunction of Rb results in a compensatory overexpression of nuclear p16 that is characteristic of HPV+ HNSCC [
8].
Evidence has demonstrated that HPV + HNSCC is distinctly different from HPV-HNSCC [
9,
10,
11,
12]. First, less heavy tobacco use or alcohol consumption is mentioned in patients with HPV+ HNSCC compared with those with HPV-HNSCC; this finding also explains why the incidence of alcohol- or cigarette-related HNSCC declines but the number of HPV + HNSCC increases [
13,
14]. Second, patients with HPV + HNSCC are younger than those with HPV-HNSCC [
15]. Third, the tumor location in these two groups is different: HPV + HNSCC is more common in the oropharynx, but other risk factors (tobacco- and alcohol-related HNSCC) more frequently arise in the oral cavity, hypopharynx, and larynx. Fourth, HPV + HNSCC has a better prognosis than HPV-HNSCC, including lower mortality and a decreased risk of relapse after treatment. A biomarker analysis study that involved a phase III trial (E1395) and a phase II trial (E3301) demonstrated that better progression-free survival (PFS) and overall survival (OS) were observed in HPV + HNSCC than in HPV-HNSCC, suggesting that HPV is a favorable prognostic factor in recurrent or metastatic HNSCC [
16]. An Eastern Cooperative Oncology Group (ECOG) phase II trial showed that patients with HPV + HNSCC had higher response rates (RRs) to induction chemotherapy and chemoradiation therapy than those with HPV-HNSCC. Additionally, the HPV + HNSCC group had an improved OS and lower risk of disease progression than the HPV-HNSCC group, indicating that tumor HPV status is strongly associated with therapeutic response and survival [
9]. Another phase II trial (E1308) that focused on induction chemotherapy followed by reduced-dose radiation and weekly cetuximab in HPV+ oropharyngeal cancer patients revealed that reduced-dose radiotherapy with concurrent cetuximab is reasonable in favorable-risk HPV + HNSCC patients who responded to induction chemotherapy, including better PFS, OS, and lower incidence of difficulty swallowing solids or impaired nutrition [
17].
Currently, HPV detection is regarded as a standard test to determine the tumor stage of oropharyngeal cancer in the eighth edition of the American Joint Committee on Cancer (AJCC) [
18]. HPV infection status is defined as positive or negative nuclear staining of p16 by immunohistochemistry; however, the role of cytoplasmic staining of p16 in the clinical outcome of HNSCC remains unclear. The present study aimed to investigate the role of p16 cytoplasmic staining in HNSCC prognosis.
2. Materials and Methods
2.1. Patient Population
Patients with HNSCC who underwent TPF induction chemotherapy at Kaohsiung Chang Gung Memorial Hospital between January 2010 and December 2015 were retrospectively reviewed. Only squamous cell carcinoma in pathology and tumors located in the oral cavity, oropharynx, hypopharynx, and larynx were included; those in nasal cavity or of unknown primary origin were excluded. Additionally, patients with a history of a second primary cancer, whether before or after the diagnosis of HNSCC, were excluded. Patients were required to receive TPF induction chemotherapy rather than other chemotherapy regimens, and those with distant metastasis or undergoing other anticancer treatments were not enrolled. Finally, 195 patients with HNSCC who met the inclusion criteria were identified.
2.2. TPF Induction Chemotherapy and Chemoradiotherapy
The TPF induction chemotherapy regimen was as follows: docetaxel 60 mg/m
2 intravenous infusion on day 1, cisplatin 60 mg/m
2 intravenous infusion on day 1, and 5-fluorouracil 600 mg/m
2 24 h intravenous infusion on days 1 to 4 every three weeks for three cycles, except in cases of intolerance to adverse events, disease progression, or withdrawal of consent by patients. Chemotherapy was administered according to a previously described protocol [
19,
20,
21].
Chemoradiotherapy (CRT) was followed by TPF induction chemotherapy in each patient. The planned radiotherapy dose for the primary tumor was 70 Gy in 35 fractions (2 Gy, 5 days per week). The doses administered to the involved lymph nodes (LNs) and uninvolved LNs were 60–70 Gy and 50 Gy, respectively.
2.3. Immunohistochemistry
Immunohistochemical staining was performed using immunoperoxidase. Staining was performed on slides (4 mm) of formalin-fixed, paraffin-embedded tissue sections using primary antibodies against p16, INK4 (BD Biosciences, San Jose, CA, USA). Briefly, after deparaffinization and rehydration, antigen retrieval was performed by treating the slides with 10 mM citrate buffer (pH 6.0) in a hot water bath (95 °C) for 20 min. Endogenous peroxidase activity was blocked for 15 min with 0.3% hydrogen peroxide. After blocking with 1% goat serum for 1 h at room temperature, sections were incubated overnight for at least 18 h with primary antibodies at 48 °C. Immunodetection was performed using an LSAB2 kit (Dako, Carpinteria, CA, USA), followed by reaction with 3-3’-diaminobenzidine for color development, and hematoxylin was used for counterstaining. Cervical carcinoma was used as a positive control, and esophageal cancer was used as a negative control. Assessment of staining was independently performed by two pathologists who were blinded to information regarding the clinicopathological features or prognosis of the patients. p16-negative (HPV-negative) expression was defined as <50% nuclear staining of tumor cells [
22,
23]. After excluding seven patients with p16-positive (HPV-positive) HNSCC, a semiquantitative immunoreactive score (IRS) was used to evaluate p16 cytoplasmic staining in 195 patients with p16-negative (HPV-negative) locally advanced HNSCC [
24]. The IRS was calculated by multiplying the staining intensity (graded as: 0 = no staining, 1 = weak staining, 2 = moderate staining, and 3 = strong staining) and the percentage of positively stained cells (0 = no stained cells, 1 = ≤10% stained cells, 2 = 10–50% stained cells, 3 = 51–80% stained cells, and 4 = ≥80% stained cells). The criterion for high p16 cytoplasmic staining was an IRS score ≥6.
2.4. Ethics Statement
This retrospective study was approved by the Chang Gung Medical Foundation Institutional Review Board (201900561B0). All procedures were performed in accordance with the ethical standards of the Institutional Research Committee and World Medical Association Declaration of Helsinki. The requirement for written informed consent was waived by the review board due to the retrospective design of this study.
2.5. Statistical Analysis
All statistical analyses in the current study were performed using SPSS software version 26 (International Business Machines Corp., Armonk, NY, USA). Differences in categorical variables were examined using the chi-square test. The Kaplan–Meier method was used for survival analysis, and the log-rank test was performed to test the differences. A Cox proportional hazards model was used to determine independent prognostic factors in the multivariate analysis. Odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to test the strength of the association between the prognostic parameters and survival. PFS was defined as the duration between the start of TPF induction chemotherapy and the date of tumor recurrence or death from any cause, without evidence of recurrence. OS was calculated from the date of HNSCC diagnosis to death or the time of last living contact. All tests were two-sided, and statistical significance was set at p < 0.05.
4. Discussion
HNSCC is an aggressive cancer and the third leading cause of mortality among men in Taiwan. Growing evidence has confirmed that HPV status is a prognostic factor for HNSCC, particularly oropharyngeal cancer [
3,
4,
5]. In general, p16 staining has been shown to predict the presence of HPV infection, and diffuse p16 unclear staining is usually considered HPV-positive [
25]. However, the role of p16 cytoplasmic staining under negative p16 nuclear expression remains unclear. Our study enrolled 195 HNSCC patients who received TPF induction chemotherapy and showed that high expression of p16 cytoplasmic staining was a more favorable predictive factor for better response to induction chemotherapy than low expression. Moreover, patients with high expression of p16 cytoplasmic staining had superior PFS and OS compared with those with low expression, regardless of tumor size, tumor stage, or tumor location. The results of our study demonstrated the prognostic role of p16 cytoplasmic staining in patients with HNSCC.
HPV has been proven to be associated with HNSCC, particularly oropharynx. A large systematic review of 39 studies with available clinical outcomes showed high heterogeneity in the diagnosis of HPV and the definition of p16. The correlation between positive HPV and overexpression of p16 was best in the group with ≥ 70% staining of p16 expression [
25]. In general, diffuse p16 nuclear and cytoplasmic staining correlates with the presence of HPV infection. However, the status of p16 cytoplasmic staining under negative presentation of p16 nuclear expression is unclear; by definition, this status should be considered as HPV−. Our study showed high expression of p16 cytoplasmic staining to be predictive of a better response to induction chemotherapy and was an independent prognostic factor for better PFS and OS when the status was HPV- HNSCC.
In contrast, in our study, the percentage of high expression of p16 cytoplasmic staining in the oropharynx was 47%, which was not different from the percentage in the oral cavity (45%) and hypopharynx/larynx (41%). However, the oral cavity was an independent predictive factor of a worse response rate (52%) to TPF induction chemotherapy, but RR was up to 68% and 64% in the oropharynx and hypopharynx/larynx, respectively. This may be related to the clinical LN metastasis status: a borderline risk factor for poor response to induction chemotherapy in our study. In the analysis of survival, although the oral cavity as tumor location was a risk factor for poor response to induction chemotherapy, the 5-year PFS rate was 29%, higher than the 23% for tumors in the oropharynx, and the 5-year OS rate was higher for tumors in the oral cavity (32%) than those in the oropharynx (27%). As mentioned above, the percentage of high p16 cytoplasmic expression could not explain these outcomes, and the difference in PFS and OS may have been related to salvage surgery. In general, salvage surgery after CRT with residual tumor or recurrence is more applicable for tumors located in the oral cavity than in the oropharynx in clinical practice. However, salvage surgery could not explain the differences in PFS and OS between the oropharynx and hypopharynx. In general, tumors arising from the oropharynx and hypopharynx/larynx are suitable for organ/function preservation therapy, and the criteria for these two organs are similar. Our data revealed that patients with tumors located in the hypopharynx/larynx had better 5-year PFS rate (41% vs. 23%) and 5-year OS rate (47% vs. 27%) than those with tumors arising from the oropharynx. This may have been related to the status of LN metastasis, as the incidence of clinical N2–3 was higher in the oropharynx group (75%) than in the hypopharynx/larynx group (69%); clinical N2–3 was an independent prognostic factor for worse PFS and OS. In addition, patients with OS for more than 9 years (long-term survival) were also analyzed. Among them, all nine patients received concurrent CRT after induction chemotherapy TPF; six patients received CR after concurrent CRT, two patients underwent bilateral neck LN dissection due to residual tumor after concurrent CRT, and the remainder (one patient) experienced recurrence after concurrent CRT and salvage surgical resection were performed.
Our study had several limitations. First, there may have been some bias due to the retrospective design of our study. Second, there was a lower percentage of women patients ( < 10%); this may be due to the higher percentage of smoking, alcohol consumption, and betel nut chewing in our study, which are more common in men than in women. However, to the best of our knowledge, the current study provides limited evidence to investigate the role of p16 cytoplasmic staining in patients with HNSCC who received TPF induction chemotherapy; our findings may demonstrate the predictive and prognostic role of p16 cytoplasmic staining in these patients in clinical practice.