Outcomes of patients with resected stage III/IV acral or mucosal melanoma, treated with adjuvant anti-PD-1 based therapy.

Details

Serval ID
serval:BIB_AD78846E78A2
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Outcomes of patients with resected stage III/IV acral or mucosal melanoma, treated with adjuvant anti-PD-1 based therapy.
Journal
European journal of cancer
Author(s)
Jacques S.K., McKeown J., Grover P., Johnson D.B., Zaremba A., Dimitriou F., Weiser R., Farid M., Namikawa K., Sullivan R.J., Rutkowski P., Lebbe C., Hamid O., Zager J.S., Michielin O., Neyns B., Nakamura Y., Robert C., Mehnert J., Ascierto P.A., Bhave P., Park B., Zimmer L., Mangana J., Mooradian M., Placzke J., Allayous C., Glitza Oliva I.C., Mehmi I., Depalo D., Wicky A., Schwarze J.K., Roy S., Boatwright C., Vanella V., Long G.V., Menzies A.M., Lo S.N., Carlino M.S.
ISSN
1879-0852 (Electronic)
ISSN-L
0959-8049
Publication state
Published
Issued date
03/2024
Peer-reviewed
Oui
Volume
199
Pages
113563
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Abstract
Acral (AM) and mucosal melanomas (MM) are rare subtypes with a poor prognosis. In those with advanced disease, anti-PD-1 (PD1) therapy has reduced activity compared to that seen in non-acral cutaneous melanoma.
To determine the efficacy of adjuvant PD1 in resected AM or MM.
An international, retrospective cohort study SETTING: Data up to November 2021 collected from 20 centres across 10 countries.
One hundred and ninety four patients with resected stage III or IV <sup>1</sup> AM or MM who received adjuvant PD1 were included and compared to matched patients from the Melanoma Institute Australia (MIA) database using a propensity score matching analysis.
Recurrence-free survival (RFS), distant metastasis-free survival (DMFS) and overall survival (OS) were investigated.
Forty five of 139 (32%) AM and 9 of 55 (16%) MM patients completed adjuvant therapy. The main reason for early treatment cessation in both groups was disease recurrence: 51 (37%) and 30 (55%) in the AM and MM groups, respectively. In the AM group adjuvant PD1 was associated with a longer RFS [HR-0.69 (0.52-0.92, p = 0.0127)], DMFS [HR0.58 (0.38-0.89, p = 0.0134)] and OS [HR of 0.59 (0.38-0.92, p-value 0.0196)] when compared to the historical cohort. In the MM group there was no statistical difference in RFS [HR1.36 (0.69-2.68,p-value 0.3799], DMFS or OS.
After adjuvant PD1, both AM and MM have a high risk of recurrence. Our data suggests a benefit to using adjuvant PD1 therapy in resected AM but not in resected MM. Additional studies to investigate the efficacy of adjuvant PD1 for MM are needed.
Keywords
Humans, Melanoma/drug therapy, Melanoma/surgery, Skin Neoplasms/drug therapy, Skin Neoplasms/surgery, Retrospective Studies, Neoplasm Recurrence, Local, Combined Modality Therapy, Acral melanoma, Adjuvant, Anti-PD1, Immunotherapy, Mucosal melanoma
Pubmed
Web of science
Create date
01/02/2024 17:02
Last modification date
06/04/2024 6:24
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