Literature DB >> 30374969

Efficacy and adverse events of five targeted agents in the treatment of advanced or metastatic non-small-cell lung cancer: A network meta-analysis of nine eligible randomized controlled trials involving 5,059 patients.

Gui-Feng Liu1, Xue-Feng Li2, Shao-Nan Yu1, Ying-Ying Miao1, Shu-Hua Zhang3.   

Abstract

Recently, targeted agents were reported to improve overall survival, progression-free survival (PFS), response rate, and quality of life compared with cytotoxic chemotherapies, which provides hope for the treatment of non-small-cell lung cancer (NSCLC). The network meta-analysis is applied to compare the efficacies and adverse events of five targeted agents (erlotinib, gefitinib, vandetanib, dacomitinib, and icotinib) for advanced or metastatic NSCLC. Nine eligible randomized controlled trials from PubMed and Cochrane Library database were included. Weighted mean difference, odds ratio, and surface under the cumulative ranking curve (SUCRA) values were evaluated for the efficacy and adverse events of the five targeted agents in the treatment of NSCLC. With regard to efficacy, the overall response rate (ORR) of advanced or metastatic NSCLC patients treated with gefitinib was relatively higher than those treated with placebo. Compared with patients treated with placebo, the disease control rate (DCR) of patients treated with erlotinib and with gefitinib was relatively higher. Furthermore, in terms of PFS and DCR, the SUCRA value of icotinib was the highest among the five targeted drugs. With regard to ORR, the SUCRA value of gefitinib was the highest among the five targeted drugs. In terms of fatigue, rash, and cough, erlotinib had the lowest SUCRA value, whereas vandetanib exhibited the lowest SUCRA value in terms of diarrhea. Our study suggests that the efficacies of gefitinib and icotinib for advanced or metastatic NSCLC were comparatively better, whereas the toxicities of erlotinib and vandetanib were relatively greater.
© 2018 Wiley Periodicals, Inc.

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Keywords:  Bayesian network model; advanced or metastatic non-small-cell lung cancer (NSCLC); adverse events; efficacy; randomized controlled trials; targeted agents

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Year:  2018        PMID: 30374969     DOI: 10.1002/jcp.26793

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  1 in total

1.  ACPA decreases non-small cell lung cancer line growth through Akt/PI3K and JNK pathways in vitro.

Authors:  Özge Boyacıoğlu; Elif Bilgiç; Cem Varan; Erem Bilensoy; Emirhan Nemutlu; Duygu Sevim; Çetin Kocaefe; Petek Korkusuz
Journal:  Cell Death Dis       Date:  2021-01-11       Impact factor: 8.469

  1 in total

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