医学
化疗
肺癌
肿瘤科
ROS1型
酪氨酸激酶
内科学
全身疗法
临床试验
酪氨酸激酶抑制剂
癌症
完全响应
细胞
肺
全身给药
药理学
前瞻性队列研究
癌症研究
激酶
呼吸道疾病
免疫学
疾病
作者
Fumihiro Kashizaki,Shohei Watanabe,Ryo Orii,Hanming Lin,J. Takeda,T Takagishi,Kentaro Yumoto,Harumi Koizumi
出处
期刊:PubMed
[National Institutes of Health]
日期:2026-07-01
卷期号:10 (7): e2600347-e2600347
摘要
PURPOSE: rearrangements occur in approximately 1%-2% of non-small cell lung cancer and define a molecular subset characterized by marked sensitivity to tyrosine kinase inhibitors (TKIs). Although ROS1 inhibitors demonstrate high response rates, the potential impact of prior systemic chemotherapy exposure before ROS1 inhibition on subsequent ROS1-TKI efficacy has not been systematically evaluated. METHODS: We conducted a systematic review and meta-analysis of prospective ROS1-TKI trials published through December 30, 2025. Outcomes were analyzed separately for TKI-naïve and post-crizotinib cohorts using random-effects models. Study-level meta-regression was performed to evaluate associations between the proportion of patients exposed to prior systemic chemotherapy and treatment response. RESULTS: = .077). No significant association was identified between prior systemic chemotherapy exposure and median progression-free survival. CONCLUSION: Beyond the expected difference between TKI-naïve and post-crizotinib cohorts, prior systemic chemotherapy exposure was associated with lower response rates to ROS1-TKIs in this study-level analysis. Although exploratory and limited by aggregate data, these findings suggest that treatment sequencing and cumulative treatment exposure may influence responsiveness to ROS1 inhibition and support early use of ROS1-directed therapy when clinically feasible.
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