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Safety and efficacy of restarting immune checkpoint inhibitors in non-small cell lung cancer patients following immune-related adverse events: a systematic review and meta-analysis.
Tan, Kexin; Wang, Aolin; Zheng, Yumin; Wang, Shuo; Wang, Chao; Li, Jia; Lu, Xingyu; Dong, Huijing; Zheng, Jiabin; Cui, Huijuan.
Affiliation
  • Tan K; Graduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
  • Wang A; Graduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
  • Zheng Y; Graduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
  • Wang S; Department of Integrative Oncology, China-Japan Friendship Hospital, Beijing, 100029, China.
  • Wang C; Department of Integrative Oncology, China-Japan Friendship Hospital, Beijing, 100029, China.
  • Li J; Graduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
  • Lu X; Graduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
  • Dong H; Graduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
  • Zheng J; Department of Integrative Oncology, China-Japan Friendship Hospital, Beijing, 100029, China. dr_zhengjiabin@foxmail.com.
  • Cui H; Department of Integrative Oncology, China-Japan Friendship Hospital, Beijing, 100029, China. cuihj1963@sina.com.
Clin Transl Oncol ; 2024 Jun 26.
Article de En | MEDLINE | ID: mdl-38922538
ABSTRACT

OBJECTIVE:

This meta-analysis aims to evaluate the safety and efficacy of restarting immune checkpoint inhibitors (ICIs) in patients with non-small cell lung cancer (NSCLC) after experiencing immune-related adverse events (irAEs).

METHODS:

A comprehensive search of PubMed, Web of Science, Embase, and the Cochrane Library was conducted to identify studies investigating the safety and efficacy of restarting ICIs in NSCLC patients after irAEs. Outcome measures, including objective response rate (ORR), progression-free survival (PFS), and overall survival (OS) after ICI restarting, were extracted. Meta-analysis was performed using the R meta-package.

RESULTS:

Four studies involving a total of 326 subjects were included, comprising 137 patients who restarted ICI treatment after irAEs and 189 patients who did not restart ICI treatment. The results revealed that ICI restarting was associated with an increased ORR (OR = 2.36, 95% CI 1.49-3.84), prolonged PFS (HR = 0.60, 95% CI 0.42-0.86), and prolonged OS (HR = 0.65, 95% CI 0.43-0.99) compared to non-restarting. The incidence of irAEs after ICI restarting was 45% (95% CI 0.27-0.63).

CONCLUSION:

Restarting ICI treatment after discontinuation due to previous irAEs appears to be a reasonable option for NSCLC patients. However, a comprehensive assessment of the potential benefits and risks to individual patients is crucial, and close monitoring of irAEs is warranted.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Clin Transl Oncol Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: Italie

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Clin Transl Oncol Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: Italie