ALK阳性非小细胞肺癌癌症中ALK抑制剂序列的系统评价。

IF 5.1 Q1 ONCOLOGY
Stephanie M Barrows, Kelly Wright, Catherine Copley-Merriman, James A Kaye, Marc Chioda, Robin Wiltshire, Knut Martin Torgersen, Elizabeth T Masters
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引用次数: 17

摘要

本研究的目的是了解使用ALK抑制剂治疗的患者的结果,特别是当ALK抑制剂之后使用其他ALK抑制剂时。截至2017年7月17日,PubMed、Embase和Cochrane进行了系统的文献综述。还检索了会议摘要(过去两年中的三次会议)。在504篇独特的出版物中,80篇符合纳入标准(47项临床试验,33项观察性研究)。观察性研究有可能为顺序使用的ALK抑制剂提供信息。10项观察性研究报告了克唑替尼引导序列的中位总生存期,从开始使用克唑替尼起为30.3至63.75个月;诊断为转移性非小细胞肺癌癌症后49.4-89.6个月;以及在首次使用克唑替尼后从第二代ALK抑制剂开始的15.5-22.0个月。ALK抑制剂的测序可能有利于使用初始ALK抑制剂进行治疗的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Systematic review of sequencing of ALK inhibitors in <i>ALK</i>-positive non-small-cell lung cancer.

Systematic review of sequencing of ALK inhibitors in ALK-positive non-small-cell lung cancer.

The objective of this study was to understand outcomes of patients treated with ALK inhibitors, especially when ALK inhibitors are followed by other ALK inhibitors. A systematic literature review was conducted in PubMed, Embase, and Cochrane through July 17, 2017. Conference abstracts (three meetings in past 2 years) also were searched. Of 504 unique publications, 80 met inclusion criteria (47 clinical trials, 33 observational studies). Observational studies have the potential to provide information for ALK inhibitors used sequentially. Ten observational studies reported median overall survival of crizotinib-led sequences ranging from 30.3 to 63.75 months from initiation of crizotinib; 49.4-89.6 months from metastatic non-small-cell lung cancer diagnosis; and 15.5-22.0 months from initiation of the second-generation ALK inhibitor after initial crizotinib. Sequencing of ALK inhibitors may benefit patients progressing on initial ALK inhibitors.

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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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