TY - JOUR
T1 - Outcomes of patients with resected stage III/IV acral or mucosal melanoma, treated with adjuvant anti-PD-1 based therapy
AU - Jacques, Sarah K.
AU - McKeown, Janet
AU - Grover, Piyush
AU - Johnson, Douglas B.
AU - Zaremba, Anne
AU - Dimitriou, Florentia
AU - Weiser, Roi
AU - Farid, Mohamad
AU - Namikawa, Kenjiro
AU - Sullivan, Ryan J.
AU - Rutkowski, Piotr
AU - Lebbe, Celeste
AU - Hamid, Omid
AU - Zager, Jonathan S.
AU - Michielin, Olivier
AU - Neyns, Bart
AU - Nakamura, Yasuhiro
AU - Robert, Caroline
AU - Mehnert, Janice
AU - Ascierto, Paolo A.
AU - Bhave, Prachi
AU - Park, Benjamin
AU - Zimmer, Lisa
AU - Mangana, Joanna
AU - Mooradian, Megan
AU - Placzke, Joanna
AU - Allayous, Clare
AU - Glitza Oliva, Isabella C.
AU - Mehmi, Inderjit
AU - Depalo, Danielle
AU - Wicky, Alexandre
AU - Schwarze, Julia K.
AU - Roy, Severine
AU - Boatwright, Christina
AU - Vanella, Vito
AU - Long, Georgina V.
AU - Menzies, Alexander M.
AU - Lo, Serigne N.
AU - Carlino, Matteo S.
N1 - Publisher Copyright:
© 2024
PY - 2024/3/1
Y1 - 2024/3/1
N2 - Importance: 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. Objective: To determine the efficacy of adjuvant PD1 in resected AM or MM. Design: An international, retrospective cohort study Setting: Data up to November 2021 collected from 20 centres across 10 countries. Participants: One hundred and ninety four patients with resected stage III or IV1 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. Main outcomes and measures: Recurrence-free survival (RFS), distant metastasis-free survival (DMFS) and overall survival (OS) were investigated. Results: 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. Conclusion and relevance: 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.
AB - Importance: 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. Objective: To determine the efficacy of adjuvant PD1 in resected AM or MM. Design: An international, retrospective cohort study Setting: Data up to November 2021 collected from 20 centres across 10 countries. Participants: One hundred and ninety four patients with resected stage III or IV1 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. Main outcomes and measures: Recurrence-free survival (RFS), distant metastasis-free survival (DMFS) and overall survival (OS) were investigated. Results: 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. Conclusion and relevance: 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.
KW - Acral melanoma
KW - Adjuvant
KW - Anti-PD1
KW - Immunotherapy
KW - Mucosal melanoma
UR - http://www.scopus.com/inward/record.url?scp=85183487463&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2024.113563
DO - 10.1016/j.ejca.2024.113563
M3 - Article
C2 - 38278007
AN - SCOPUS:85183487463
SN - 0959-8049
VL - 199
JO - European Journal of Cancer
JF - European Journal of Cancer
M1 - 113563
ER -