Metastatic Melanoma: Current Status and Future Prospects

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Cancer Biology and Oncology".

Deadline for manuscript submissions: closed (29 February 2024) | Viewed by 4476

Special Issue Editors


E-Mail Website
Guest Editor
1. Institute of Oncology Ljubljana, Zaloska 2, 1000 Ljubljana, Slovenia
2. Faculty of Medicine, University of Ljubljana, Zaloska 2, 1000 Ljubljana, Slovenia
Interests: cutaneous melanoma; skin cancer; melanoma molecular markers; hereditary cancer syndromes

E-Mail Website
Guest Editor
National Research Council—Institute of Translational Pharmacology (CNR-IFT), Via Fosso del Cavaliere 100, Rome, Italy
Interests: gene electrotransfer; cancer gene therapy; electroporation; plasmid DNA; electrochemotherapy
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Cutaneous melanoma is not the most common skin cancer but it is the most significant cause of skin cancer mortality. Studies such as MSLT II showed that approximately 30% of patients with stage III will progress and develop distant metastases. Just a decade ago, such progression was treated with cytotoxic chemotherapy with a single agent or in combination, which in some regimes included high-doses of interleukin 2 (IL-2). The success of such treatments was limited. Only 5-10% of individuals responded to drugs and the prognosis of patients was dismal, with medium survival measured in months.

In 2011, the US FDA approved the first two drugs for the treatment of metastatic cutaneous melanoma: the CTLA-4 inhibitor ipilimumab and the BRAF inhibitor vemurafenib. Since then, additional check point inhibitors and molecularly targeted agents have been tested and approved in a metastatic setting. Consequently, the goals of treatment have changed from palliation to effective and even durable clinical disease control for the majority of patients. Despite these achievements, clinicians sometimes still struggle with the most appropriate first line treatment in the case of metastatic cutaneous melanoma: choosing from novel systemic therapies while trying not to neglect the role of surgery and radiotherapy.

The key to understanding therapy failure and drug resistance lies in understanding the molecular pathways responsible for the development and progression of melanoma, as well as the relevance of detecting the specific molecular markers of each cutaneous melanoma subtype.

We hope, that this Special Issue, which will include novel insights into cutaneous melanoma translational research, targeted molecular research, molecular biomarkers and immunotherapy, will add valuable pieces to the puzzle of the rapidly evolving treatment landscape of metastatic disease. 

Dr. Barbara Perić
Prof. Dr. Maja Čemažar
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Biomedicines is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • cutaneous melanoma
  • distant metastases
  • molecular pathways, biomarkers, driver genes
  • targeted therapy
  • check point inhibitors
  • systemic toxicity

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Review

Jump to: Other

19 pages, 787 KiB  
Review
Enhancing Immunogenicity in Metastatic Melanoma: Adjuvant Therapies to Promote the Anti-Tumor Immune Response
by Sandra Pelka and Chandan Guha
Biomedicines 2023, 11(8), 2245; https://doi.org/10.3390/biomedicines11082245 - 10 Aug 2023
Cited by 2 | Viewed by 1530
Abstract
Advanced melanoma is an aggressive form of skin cancer characterized by low survival rates. Less than 50% of advanced melanoma patients respond to current therapies, and of those patients that do respond, many present with tumor recurrence due to resistance. The immunosuppressive tumor-immune [...] Read more.
Advanced melanoma is an aggressive form of skin cancer characterized by low survival rates. Less than 50% of advanced melanoma patients respond to current therapies, and of those patients that do respond, many present with tumor recurrence due to resistance. The immunosuppressive tumor-immune microenvironment (TIME) remains a major obstacle in melanoma therapy. Adjuvant treatment modalities that enhance anti-tumor immune cell function are associated with improved patient response. One potential mechanism to stimulate the anti-tumor immune response is by inducing immunogenic cell death (ICD) in tumors. ICD leads to the release of damage-associated molecular patterns within the TIME, subsequently promoting antigen presentation and anti-tumor immunity. This review summarizes relevant concepts and mechanisms underlying ICD and introduces the potential of non-ablative low-intensity focused ultrasound (LOFU) as an immune-priming therapy that can be combined with ICD-inducing focal ablative therapies to promote an anti-melanoma immune response. Full article
(This article belongs to the Special Issue Metastatic Melanoma: Current Status and Future Prospects)
Show Figures

Figure 1

Other

Jump to: Review

10 pages, 570 KiB  
Case Report
Dabrafenib-Trametinib and Radiotherapy for Oligoprogressive BRAF Mutant Advanced Melanoma
by Ernesto Rossi, Giovanni Schinzari, Francesco Cellini, Mario Balducci, Mariangela Pasqualoni, Brigida Anna Maiorano, Bruno Fionda, Silvia Longo, Francesco Deodato, Alessandro Di Stefani, Ketty Peris, Maria Antonietta Gambacorta and Giampaolo Tortora
Biomedicines 2023, 11(2), 394; https://doi.org/10.3390/biomedicines11020394 - 29 Jan 2023
Cited by 1 | Viewed by 2458
Abstract
The clinical management of metastatic melanoma has been changed by BRAF (BRAFi) and MEK inhibitors (MEKi), which represent a standard treatment for BRAF-mutant melanoma. In oligoprogressive melanoma patients with BRAF mutations, target therapy can be combined with loco-regional radiotherapy (RT). However, the [...] Read more.
The clinical management of metastatic melanoma has been changed by BRAF (BRAFi) and MEK inhibitors (MEKi), which represent a standard treatment for BRAF-mutant melanoma. In oligoprogressive melanoma patients with BRAF mutations, target therapy can be combined with loco-regional radiotherapy (RT). However, the association of BRAF/MEK inhibitors and RT needs to be carefully monitored for potential increased toxicity. Despite the availability of some reports regarding the tolerability of RT + target therapy, data on simultaneous RT and BRAFi/MEKi are limited and mostly focused on the BRAFi vemurafenib. Here, we report a series of metastatic melanoma patients who received fractioned RT regimens for oligoprogressive disease in combination with the BRAFi dabrafenib and the MEKi trametinib, which have continued beyond progression. None of the cases developed relevant adverse events while receiving RT or interrupted dabrafenib and trametinib administration. These cases suggest that a long period of dabrafenib/trametinib interruption during radiotherapy for oligoprogressive disease can be avoided. Prospective trials are warranted to assess the efficacy and safety of the contemporary administration of BRAF/MEK inhibitors and radiotherapy for oligoprogressive disease. Full article
(This article belongs to the Special Issue Metastatic Melanoma: Current Status and Future Prospects)
Show Figures

Figure 1

Back to TopTop