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Serious Immune-related Adverse Events Are Associated With Greater Efficacy of Nivolumab Therapy Against Non-small Cell Lung Cancer
J. Blazek, P. Hosek, K. Hrabcova, M. Bratova, J. Kultan, M. Hrnciarik, M. Cernovska, P. Zemanova, J. Krejci, L. Koubkova, M. Stastny, M. Svaton
Status neindexováno Jazyk angličtina Země Řecko
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 2004 do Před 2 roky
PubMed Central
od 2017
Europe PubMed Central
od 2017
Open Access Digital Library
od 2004-01-01
PubMed
37652490
DOI
10.21873/invivo.13324
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
BACKGROUND/AIM: The aim of this study was to investigate possible association between adverse events of nivolumab therapy and the effectiveness of treatment in patients with non-small cell lung cancer (NSCLC). Focusing on serious adverse events (i.e., those of grade ≥3), we evaluated overall survival (OS), progression-free survival (PFS), as well as objective response rate (ORR) to treatment. PATIENTS AND METHODS: We retrospectively analyzed a set of patients from the TULUNG database of NSCLC treated with nivolumab in eight oncology centers. We evaluated OS data based upon this set. To reduce possible bias, we further evaluated a subgroup of patients treated at the University Hospital in Pilsen, where the occurrence of adverse events, PFS, and ORR were independently examined by two experienced physicians. Survival statistics were evaluated using the Kaplan-Meier method and Cox analysis. RESULTS: We observed significantly greater OS, PFS, and ORR in the group of patients experiencing adverse events upon nivolumab treatment versus in those patients without such events. Although the univariable model analyzing the data set of all patients demonstrated higher OS in patients with serious adverse events, only a nonsignificant trend was observed in the Cox multivariable model. In a subgroup of patients with PFS and ORR evaluation, we did observe significant, favorable effects for patients having had serious adverse effects. CONCLUSION: Patients experiencing severe adverse events show a tendency toward better OS, PFS, and ORR compared to patients without or having only mild adverse events with nivolumab treatment.
BMS Czech Republic Prague Czech Republic
Department of Oncology 1st Faculty of Medicine Prague Charles University Prague Czech Republic
Department of Respiratory Diseases Faculty of Medicine Masaryk University Brno Czech Republic
Department of Respiratory Medicine Faculty of Medicine Palacky University Olomouc Czech Republic
Department of Respiratory Medicine Thomayer Hospital Prague Czech Republic
Institute of Biostatistics and Analyses Ltd Brno Czech Republic
Citace poskytuje Crossref.org
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