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Chemotherapy after immune checkpoint inhibitor failure in metastatic melanoma: a retrospective multicentre analysis

医学 达卡巴嗪 化疗 内科学 肿瘤科 黑色素瘤 卡铂 替莫唑胺 进行性疾病 无进展生存期 外科 癌症研究 顺铂
作者
Simone M. Goldinger,Kristina Buder‐Bakhaya,Serigne Lo,Andrea Forschner,Meredith McKean,Lisa Zimmer,Chloe Khoo,Reinhard Dummer,Zeynep Eroglu,Elizabeth I. Buchbinder,Paolo A. Ascierto,Ralf Gutzmer,Elisa A. Rozeman,Christoph Höeller,Douglas B. Johnson,Anja Gesierich,Peter Kölblinger,Naima Bennannoune,Justine V. Cohen,Katharina C. Kähler,Melissa Wilson,Jonathan Cebon,Victoria Atkinson,Jessica L. Smith,Olivier Michielin,Georgina V. Long,Jessica C. Hassel,Benjamin Weide,Lauren E. Haydu,Dirk Schadendorf,Grant A. McArthur,Patrick A. Ott,Christian U. Blank,Caroline Robert,Ryan J. Sullivan,Axel Hauschild,Matteo S. Carlino,Claus Garbe,Michael A. Davies,Alexander M. Menzies
出处
期刊:European Journal of Cancer [Elsevier]
卷期号:162: 22-33 被引量:35
标识
DOI:10.1016/j.ejca.2021.11.022
摘要

Despite remarkably improved outcomes with immune checkpoint inhibition, many patients with metastatic melanoma will eventually require further therapy. Chemotherapy has limited activity when used first-line but can alter the tumour microenvironment and does improve efficacy when used in combination with immunotherapy in lung cancer. Whether chemotherapy after checkpoint inhibitor failure has relevant activity in patients with metastatic melanoma is unknown.Patients with metastatic melanoma treated with chemotherapy after progression on immunotherapy with checkpoint inhibitors were identified retrospectively from 24 melanoma centres. Objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and safety were examined.In total, 463 patients were treated between 2007 and 2017. Fifty-six per cent had received PD-1-based therapy before chemotherapy. Chemotherapy regimens included carboplatin + paclitaxel (32%), dacarbazine (25%), temozolomide (15%), taxanes (9%, nab-paclitaxel 4%), fotemustine (6%) and others (13%). Median duration of therapy was 7.9 weeks (0-108). Responses included 0.4% complete response (CR), 12% partial response (PR), 21% stable disease (SD) and 67% progressive disease (PD). Median PFS was 2.6 months (2.2, 3.0), and median PFS in responders was 8.7 months (6.3, 16.3), respectively. Twelve-month PFS was 12% (95% CI 2-15%). In patients who had received anti-PD-1 before chemotherapy, the ORR was 11%, and median PFS was 2.5 months (2.1, 2.8). The highest activity was achieved with single-agent taxanes (N = 40), with ORR 25% and median PFS 3.9 months (2.1, 6.2). Median OS from chemotherapy start was 7.1 months (6.5, 8.0). Subsequent treatment with checkpoint inhibitors achieved a response rate of 16% with a median PFS of 19.1 months (2.0-43.1 months). No unexpected toxicities were observed.Chemotherapy has a low response rate and short PFS in patients with metastatic melanoma who have failed checkpoint inhibitor therapy, although activity varied between regimens. Chemotherapy has a limited role in the management of metastatic melanoma.
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