Jacques Sarah K, McKeown Janet, Grover Piyush, Johnson Douglas B, Zaremba Anne, Dimitriou Florentia, Weiser Roi, Farid Mohamad, Namikawa Kenjiro, Sullivan Ryan J, Rutkowski Piotr, Lebbe Celeste, Hamid Omid, Zager Jonathan S, Michielin Olivier, Neyns Bart, Nakamura Yasuhiro, Robert Caroline, Mehnert Janice, Ascierto Paolo A, Bhave Prachi, Park Benjamin, Zimmer Lisa, Mangana Joanna, Mooradian Megan, Placzke Joanna, Allayous Clare, Glitza Oliva Isabella C, Mehmi Inderjit, Depalo Danielle, Wicky Alexandre, Schwarze Julia K, Roy Severine, Boatwright Christina, Vanella Vito, Long Georgina V, Menzies Alexander M, Lo Serigne N, Carlino Matteo S
Department of Medical Oncology, Westmead and Blacktown Hospitals, Sydney, Australia.
Melanoma Institute Australia, The University of Sydney, Sydney, Australia.
Eur J Cancer. 2024 Mar;199:113563. doi: 10.1016/j.ejca.2024.113563. Epub 2024 Jan 22.
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 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.
肢端黑色素瘤(AM)和黏膜黑色素瘤(MM)是罕见的亚型,预后较差。在晚期疾病患者中,与非肢端皮肤黑色素瘤相比,抗程序性死亡蛋白1(PD-1)治疗的活性降低。
确定辅助性PD-1治疗对已切除的AM或MM的疗效。
一项国际回顾性队列研究
收集了截至2021年11月来自10个国家20个中心的数据。
纳入194例接受辅助性PD-1治疗的已切除III期或IV期AM或MM患者,并使用倾向评分匹配分析与澳大利亚黑色素瘤研究所(MIA)数据库中的匹配患者进行比较。
研究无复发生存期(RFS)、无远处转移生存期(DMFS)和总生存期(OS)。
139例AM患者中有45例(32%)和55例MM患者中有9例(16%)完成了辅助治疗。两组早期治疗中断的主要原因是疾病复发:AM组和MM组分别为51例(37%)和30例(55%)。与历史队列相比,AM组辅助性PD-1治疗与更长的RFS[风险比(HR)为0.69(0.52-0.92,p=0.0127)]、DMFS[HR为0.58(0.38-0.89,p=0.0134)]和OS[HR为0.59(0.38-0.92,p值=0.0196)]相关。MM组在RFS[HR为1.36(0.69-2.68,p值=0.3799)]、DMFS或OS方面无统计学差异。
辅助性PD-1治疗后,AM和MM均有较高的复发风险。我们的数据表明,辅助性PD-1治疗对已切除的AM有益,但对已切除的MM无益。需要进一步研究来探讨辅助性PD-1治疗对MM的疗效。