Mengmeng Zhao, Jian Zhang, Jie Gao, Jianping Wang, Zhenkai Ma
{"title":"Osimertinib Efficacy and Safety in Treating Epidermal Growth Factor Receptor Mutation-Positive Advanced Non-Small-Cell Lung Cancer: A Meta-Analysis.","authors":"Mengmeng Zhao, Jian Zhang, Jie Gao, Jianping Wang, Zhenkai Ma","doi":"10.1002/cpdd.1483","DOIUrl":null,"url":null,"abstract":"<p><p>This study compared the safety and efficacy of osimertinib, a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI), with those of other TKIs and its use alongside bevacizumab in patients with EGFR mutation-positive advanced non-small-cell lung cancer. PubMed, Embase, Cochrane Library, Web of Science, China National Knowledge Infrastructure, Wanfang, and VIP databases were used to conduct extensive searches for relevant randomized controlled trials until January 30, 2024. Osimertinib monotherapy favored disease control rate, whereas the comparator treatment arm favored overall survival. Using subgroup analysis, the objective response rate and progression-free survival (PFS) were significantly elevated by Osimertinib monotherapy compared with pemetrexed combined with carboplatin or cisplatin. The comparator treatment arm receiving gefitinib or erlotinib significantly favored progression-free survival and overall survival compared with osimertinib monotherapy. In patients treated with osimertinib monotherapy, the incidence of all adverse events (AEs) decreased compared with comparator treatment arm. Anemia was the only AE associated with osimertinib monotherapy. Pemetrexed combined with carboplatin or cisplatin resulted in greater loss of appetite than osimertinib monotherapy. The most associated AE of osimertinib monotherapy was diarrhea, according to network analysis. Although its efficacy is not consistent with other EGFR TKIs, osimertinib was associated with a decrease in AEs in patients with EGFR mutation-positive advanced non-small-cell lung cancer.</p>","PeriodicalId":10495,"journal":{"name":"Clinical Pharmacology in Drug Development","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Pharmacology in Drug Development","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/cpdd.1483","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
This study compared the safety and efficacy of osimertinib, a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI), with those of other TKIs and its use alongside bevacizumab in patients with EGFR mutation-positive advanced non-small-cell lung cancer. PubMed, Embase, Cochrane Library, Web of Science, China National Knowledge Infrastructure, Wanfang, and VIP databases were used to conduct extensive searches for relevant randomized controlled trials until January 30, 2024. Osimertinib monotherapy favored disease control rate, whereas the comparator treatment arm favored overall survival. Using subgroup analysis, the objective response rate and progression-free survival (PFS) were significantly elevated by Osimertinib monotherapy compared with pemetrexed combined with carboplatin or cisplatin. The comparator treatment arm receiving gefitinib or erlotinib significantly favored progression-free survival and overall survival compared with osimertinib monotherapy. In patients treated with osimertinib monotherapy, the incidence of all adverse events (AEs) decreased compared with comparator treatment arm. Anemia was the only AE associated with osimertinib monotherapy. Pemetrexed combined with carboplatin or cisplatin resulted in greater loss of appetite than osimertinib monotherapy. The most associated AE of osimertinib monotherapy was diarrhea, according to network analysis. Although its efficacy is not consistent with other EGFR TKIs, osimertinib was associated with a decrease in AEs in patients with EGFR mutation-positive advanced non-small-cell lung cancer.
本研究比较了第三代表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI)奥西莫替尼与其他TKI的安全性和有效性,以及奥西莫替尼与贝伐珠单抗一起用于EGFR突变阳性晚期非小细胞肺癌患者的安全性和有效性。我们利用PubMed、Embase、Cochrane Library、Web of Science、中国国家知识基础设施、万方数据库和VIP数据库对截至2024年1月30日的相关随机对照试验进行了广泛检索。奥希替尼单药治疗有利于疾病控制率,而对比治疗组则有利于总生存率。通过亚组分析,与培美曲塞联合卡铂或顺铂相比,奥希替尼单药治疗的客观反应率和无进展生存期(PFS)显著提高。与奥希替尼单药治疗相比,接受吉非替尼或厄洛替尼治疗的对比治疗组的无进展生存期和总生存期明显更长。在接受奥希替尼单药治疗的患者中,所有不良事件(AEs)的发生率均低于对比治疗组。贫血是唯一与奥希替尼单药治疗相关的不良反应。与奥希替尼单药治疗相比,培美曲塞联合卡铂或顺铂治疗会导致更严重的食欲不振。根据网络分析,奥希替尼单药治疗最常见的不良反应是腹泻。虽然奥希替尼的疗效与其他表皮生长因子受体TKIs不一致,但奥希替尼可减少表皮生长因子受体突变阳性晚期非小细胞肺癌患者的AEs。
期刊介绍:
Clinical Pharmacology in Drug Development is an international, peer-reviewed, online publication focused on publishing high-quality clinical pharmacology studies in drug development which are primarily (but not exclusively) performed in early development phases in healthy subjects.