| Literature DB >> 32117727 |
Reut Hadash-Bengad1, Emma Hajaj1, Shiri Klein1, Sharon Merims1, Stephen Frank1, Galit Eisenberg1, Alexander Yakobson2, Marina Orevi3, Nadia Caplan4, Tamar Peretz1, Michal Lotem1, Jonatan E Cohen1,5.
Abstract
Melanoma survival increased with targeted- and immunotherapy agents, yet most patients ultimately progress and require salvage therapy. In our experience, some progressive disease patients on immune-checkpoint inhibitors (ICIs) demonstrate deep and sustained responses to chemotherapy. We hypothesized that ICIs improve the response to subsequent chemotherapy in metastatic melanoma. We conducted a retrospective study to compare the efficacy of chemotherapy given with prior immunotherapy, to its efficacy given without it. We measured progression free survival (PFS), overall survival, and response rate. Immune-monitoring was performed on sequential peripheral blood mononuclear cell samples taken from a chemotherapy-responsive patient. The chemotherapy post-immunotherapy group (CpI) included 11 patients, the chemotherapy without prior immunotherapy (CNPI) group included 24 patients. Median PFS was 5.2 months in the CpI vs. 2.5 months in the CNPI groups; HR 0.37 [95% Confidence interval (CI) 0.144-0.983], P = 0.046. Immune-monitoring showed an increased proportion of CD8+ cells, with elevated PD-1 and CD69 expression, while on chemotherapy, as compared with all-time points on ICIs, suggesting immune-activation. Immunotherapy potentiates the effect of chemotherapy in metastatic melanoma possibly through activation of CD8+ T cells.Entities:
Keywords: chemotherapy; immune checkpoint inhibitors; immune-monitoring; malignant melanoma; salvage therapy
Year: 2020 PMID: 32117727 PMCID: PMC7033746 DOI: 10.3389/fonc.2020.00070
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244