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Journal article : Review

Comparative Insights into Cutaneous, Mucosal, and Vulvovaginal Melanomas: Biology, Targeted Therapies, and Survival with a Focus on Immune Checkpoint Inhibitors

Abstract:
Background/Objectives: Melanoma is a malignant tumour of melanocytes. Cutaneous melanoma accounts for the vast majority of cases and has benefitted from advances in targeted and immune checkpoint inhibitor therapies, leading to substantial improvements in survival. In contrast, mucosal and vulvovaginal melanomas are rare, aggressive subtypes with distinct molecular and immune profiles and poor prognoses. This review synthesises evidence comparing cutaneous, mucosal, and vulvovaginal melanoma, with emphasis on biology, treatment, and outcomes Methods: A narrative comparative review was undertaken, examining the published literature on the epidemiology, molecular and immune characteristics, and treatment outcomes of cutaneous, mucosal, and vulvovaginal melanoma, including systemic therapies and surgical approaches. Results: Cutaneous melanoma demonstrates high tumour mutational burden and frequent BRAF and NRAS mutations, underpinning the success of targeted therapy and immunotherapy. Mucosal and vulvovaginal melanomas exhibit lower mutational burden, distinct mutation patterns, and reduced immunogenicity, correlating with poorer treatment responses. Surgery remains the mainstay of management, though optimal margins in vulvovaginal melanoma are unclear. Recurrence rates are high, and five-year survival remains poor. Evidence for systemic therapy is limited to small retrospective cohorts and subgroup analyses, showing lower response and survival rates compared with cutaneous melanoma. Chemotherapy has minimal benefit. Conclusions: Mucosal and vulvovaginal melanomas are biologically and clinically distinct from cutaneous melanoma and continue to have poor survival outcomes. Their rarity restricts high-quality evidence, highlighting the need for collaborative, innovative research to inform effective treatment strategies.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3390/jpm15110551

Authors

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Institution:
University of Oxford
Role:
Author
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-2801-2786
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Role:
Author
ORCID:
0000-0001-7106-0834
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Role:
Author
ORCID:
0009-0009-3002-2079


Publisher:
MDPI
Journal:
Journal of Personalized Medicine More from this journal
Volume:
15
Issue:
11
Pages:
551
Publication date:
2025-11-12
Acceptance date:
2025-11-01
DOI:
EISSN:
2075-4426
ISSN:
2075-4426
Pmid:
41295253


Language:
English
Keywords:
Subtype:
Review
Pubs id:
2350416
UUID:
uuid_20085085-6906-4fb6-8ec3-f8e17e0e4c25
Local pid:
pubs:2350416
Source identifiers:
3532624
Deposit date:
2025-12-04
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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