TY - JOUR
T1 - Chemotherapy after immune checkpoint inhibitor failure in metastatic melanoma
T2 - a retrospective multicentre analysis
AU - Goldinger, Simone M.
AU - Buder-Bakhaya, Kristina
AU - Lo, Serigne N.
AU - Forschner, Andrea
AU - McKean, Meredith
AU - Zimmer, Lisa
AU - Khoo, Chloe
AU - Dummer, Reinhard
AU - Eroglu, Zeynep
AU - Buchbinder, Elizabeth I.
AU - Ascierto, Paolo A.
AU - Gutzmer, Ralf
AU - Rozeman, Elisa A.
AU - Hoeller, Christoph
AU - Johnson, Douglas B.
AU - Gesierich, Anja
AU - Kölblinger, Peter
AU - Bennannoune, Naima
AU - Cohen, Justine V.
AU - Kähler, Katharina C.
AU - Wilson, Melissa A.
AU - Cebon, Jonathan
AU - Atkinson, Victoria
AU - Smith, Jessica L.
AU - Michielin, Olivier
AU - Long, Georgina V.
AU - Hassel, Jessica C.
AU - Weide, Benjamin
AU - Haydu, Lauren E.
AU - Schadendorf, Dirk
AU - McArthur, Grant
AU - Ott, Patrick A.
AU - Blank, Christian
AU - Robert, Caroline
AU - Sullivan, Ryan
AU - Hauschild, Axel
AU - Carlino, Matteo S.
AU - Garbe, Claus
AU - Davies, Michael A.
AU - Menzies, Alexander M.
N1 - Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2022/2/1
Y1 - 2022/2/1
N2 - Introduction: 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. Methods: 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. Results: 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. Conclusion: 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.
AB - Introduction: 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. Methods: 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. Results: 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. Conclusion: 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.
KW - Anti-PD-1 antibodies
KW - Cancer
KW - Checkpoint inhibitors
KW - Chemotherapy
KW - Immunotherapy
KW - Melanoma
UR - http://www.scopus.com/inward/record.url?scp=85121553444&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2021.11.022
DO - 10.1016/j.ejca.2021.11.022
M3 - Article
C2 - 34952480
AN - SCOPUS:85121553444
SN - 0959-8049
VL - 162
SP - 22
EP - 33
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -