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Treatment-related adverse events of PD-1/PD-L1 inhibitors combined with CTLA-4 inhibitors in clinical trials: a meta-analysis.
Mi, Ze; Zhang, Yunshu; Feng, Zhichao; Liu, Jiahao; Wu, Jianmin; Tan, Hongpei; Ma, Xiaoqian; Liu, Zhenguo; Rong, Pengfei.
Afiliação
  • Mi Z; Department of Radiology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Zhang Y; Xiangya School of Medicine, Central South University, Changsha, China.
  • Feng Z; Department of Radiology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Liu J; Department of Radiology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Wu J; Department of Radiology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Tan H; Department of Radiology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Ma X; Department of Radiology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Liu Z; Department of Infectious Disease, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Rong P; Department of Radiology, The Third Xiangya Hospital, Central South University, Changsha, China.
Artif Cells Nanomed Biotechnol ; 50(1): 301-309, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36217590
ABSTRACT

AIM:

PD-1/PD-L1 inhibitors in combination with CTLA-4 inhibitors are being tested in a number of ongoing clinical trials. As a result, it is critical to fully comprehend the toxicity characteristics of adverse events in combination therapy. This study aims to extensively compare the incidences and ORs of treatment-related adverse events between two combination strategies.

METHODS:

The eligible articles were searched from PubMed, EMBASE and Cochrane databases for studies published between 1 January 2010 and 1 May 2021, investigating PD-1/PD-L1 inhibitors plus CTLA-4 inhibitor-based combined clinical therapies. The mean incidences and pooled ORs of all-grade and grade 3 or higher adverse events were calculated by random-effects model using Stata 12.1. Heterogeneity between studies was assessed with I2 statistics and Chi square-based Q statistic. The overall risk of bias was assessed by Review Manager 5.3.

RESULTS:

A total of 26 eligible studies of 3607 patients were selected; 2852 patients developed at least one all-grade adverse event. PD-L1 inhibitors plus CTLA-4 inhibitors regimen (incidence 0.67, 95% CI 0.57-0.77) had marked advantage over PD-1 inhibitors plus CTLA-4 inhibitors regimen (incidence 0.89, 95% CI 0.86-0.93).

CONCLUSION:

PD-L1 inhibitors plus CTLA-4 inhibitors shows better safety in treatment-related adverse events than PD-1 inhibitors plus CTLA-4 inhibitors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptor de Morte Celular Programada 1 / Inibidores de Checkpoint Imunológico Tipo de estudo: Incidence_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptor de Morte Celular Programada 1 / Inibidores de Checkpoint Imunológico Tipo de estudo: Incidence_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article