4.7 Article

Mean platelet volume, thrombocytosis, and survival in non-small cell lung cancer patients treated with first-line pembrolizumab alone or with chemotherapy

Journal

CANCER IMMUNOLOGY IMMUNOTHERAPY
Volume 72, Issue 7, Pages 2067-2074

Publisher

SPRINGER
DOI: 10.1007/s00262-023-03392-9

Keywords

Mean platelet volume; Platelets; Immunotherapy; Non-small cell lung cancer; Overall survival; Immune-related adverse events

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This study investigated the association between the change in mean platelet volume (MPV) and survival as well as the risk of developing immune-related adverse events (irAEs) in patients with metastatic non-small cell lung cancer (NSCLC) who received first-line immune checkpoint inhibitors (ICIs). The study found that a decrease in MPV was associated with higher survival rates, while a decrease in MPV was associated with a higher risk of developing irAEs.
IntroductionPatients treated with immune checkpoint inhibitors (ICIs) may not response to treatment and are at risk for immune-related adverse events (irAEs). Platelet function has been linked to both oncogenesis and immune evasion. We studied the association between the change in mean platelet volume (MPV), platelet count, survival, and the risk of developing irAEs in patients with metastatic non-small cell lung cancer (NSCLC) who have received first-line ICI.MethodsIn this retrospective study, delta ( increment ) MPV was defined as the difference between cycle 2 and baseline MPV. Patient data were collected via chart review, and Cox proportional hazard and Kaplan-Meier method were used to assess the risk and estimate median overall survival.ResultsWe identified 188 patients treated with first-line pembrolizumab, with or without concurrent chemotherapy. There were 80 (42.6%) patients received pembrolizumab monotherapy, and 108 (57.4%) received pembrolizumab in combination with platinum-based chemotherapy. Patients whose MPV ( increment MPV <= 0) decreased had hazard ratio (HR) = 0.64 (95% CI 0.43-0.94) for death with p = 0.023. Patients with increment MPV <= - 0.2 fL (median), there was a 58% increase in the risk of developing irAE (HR = 1.58, 95% CI 1.04-2.40, p = 0.031). Thrombocytosis at baseline and cycle 2 was associated with shorter OS with p = 0.014 and 0.039, respectively.ConclusionChange in MPV after 1 cycle of pembrolizumab-based treatment was significantly associated with overall survival as well as the occurrence of irAEs in patients with metastatic NSCLC in the first-line setting. In addition, thrombocytosis was associated with poor survival.

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