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

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

Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 02 09 2022
accepted: 29 01 2023
medline: 15 6 2023
pubmed: 17 2 2023
entrez: 16 2 2023
Statut: ppublish

Résumé

Patients 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. In this retrospective study, delta (∆) 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. We 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 (∆MPV ≤ 0) decreased had hazard ratio (HR) = 0.64 (95% CI 0.43-0.94) for death with p = 0.023. Patients with ∆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. Change 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.

Identifiants

pubmed: 36795122
doi: 10.1007/s00262-023-03392-9
pii: 10.1007/s00262-023-03392-9
doi:

Substances chimiques

pembrolizumab DPT0O3T46P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2067-2074

Subventions

Organisme : NIH HHS
ID : P30CA016058
Pays : United States
Organisme : NIH HHS
ID : P30CA016058
Pays : United States
Organisme : NIH HHS
ID : P30CA016058
Pays : United States
Organisme : NIH HHS
ID : P30CA016058
Pays : United States
Organisme : NIH HHS
ID : P30CA016058
Pays : United States

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Mingjia Li (M)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA. Mingjia.Li@OSUMC.EDU.

Songzhu Zhao (S)

Department of Biomedical Informatics, Center for Biostatistics, The Ohio State University, Columbus, USA.

Gabrielle Lopez (G)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Austin Secor (A)

College of Medicine, The Ohio State University, Columbus, USA.

Parthib Das (P)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Nitya Surya (N)

College of Medicine, The Ohio State University, Columbus, USA.

Madison Grogan (M)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Sandip Patel (S)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Karthik Chakravarthy (K)

College of Medicine Medical Scientist Training Program, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

Abdul Miah (A)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Daniel Spakowicz (D)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

Gabriel Tinoco (G)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Zihai Li (Z)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

Lai Wei (L)

Department of Biomedical Informatics, Center for Biostatistics, The Ohio State University, Columbus, USA.

Kai He (K)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

Erin Bertino (E)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Asrar Alahmadi (A)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Regan Memmott (R)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Jacob Kaufman (J)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

Peter G Shields (PG)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

David P Carbone (DP)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

Carolyn J Presley (CJ)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

Gregory A Otterson (GA)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.

Dwight H Owen (DH)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus, USA.
Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, USA.

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