| Literature DB >> 33757838 |
Yi Zhao1, Bo Cheng1, Zisheng Chen2, Jianfu Li1, Hengrui Liang1, Ying Chen1, Feng Zhu1, Caichen Li1, Ke Xu1, Shan Xiong1, Weixiang Lu1, Zhuxing Chen1, Ran Zhong1, Shen Zhao3, Zhanhong Xie4, Jun Liu1, Wenhua Liang5, Jianxing He6.
Abstract
Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are treatments commonly used for lung cancer. The toxicity profile including toxicity incidence, severity, and spectrum (involving various specific adverse events) of each EGFR-TKI are of particular clinical interest and importance. Data from phase II and III randomized controlled trials comparing treatments among EGFR-TKIs (osimertinib, dacomitinib, afatinib, erlotinib, gefitinib, and icotinib) and chemotherapy for lung cancer were synthesized with Bayesian network meta-analysis. The primary outcome was systemic all-grade and grade ≥3 adverse events. The secondary outcome was specific all-grade adverse events including those of the skin, gastrointestinal tract, lung, etc. 40 trials randomizing 13,352 patients were included. Generally greater toxicity for dacomitinib and afatinib, and safety for icotinib were suggested. Furthermore, we found individual EGFR-TKIs had different toxicity spectrums. These findings provide a compelling safety reference for the individualized use of EGFR-TKIs for patients with lung cancer.Entities:
Keywords: Adverse event; EGFR; Lung cancer; Network meta-analysis; Toxicity
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Year: 2021 PMID: 33757838 DOI: 10.1016/j.critrevonc.2021.103305
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312