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肿瘤学中使用的酪氨酸激酶抑制剂疗效和安全性的种族间差异:来自3期临床试验的见解

Inter-Ethnic Differences in the Efficacy and Safety of Tyrosine Kinase Inhibitors Used in Oncology: Insights From Phase 3 Clinical Trials.

作者信息

Kyriacou Nicki M, Gross Annette S, McLachlan Andrew J

机构信息

Sydney Pharmacy School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.

出版信息

Clin Transl Sci. 2025 May;18(5):e70224. doi: 10.1111/cts.70224.

Abstract

Differences in the efficacy and safety of tyrosine kinase inhibitors (TKIs) have been observed across ethnic/ancestry subpopulations (previously reviewed to 2017). With an expanding number of TKIs approved since that time, an updated review of TKI response across ethnic/ancestry subpopulations in Phase 3 TKI clinical trials was conducted. A total of 73 population subgroup analyses (defined by participant race, ethnicity, ancestry or geographic region) of progression-free survival (PFS) and/or overall survival (OS) were identified by a literature search. Twelve (16%) of the analyses investigating the efficacy of afatinib, brigatinib, dacomitinib, gilteritinib, lorlatinib, neratinib, osimertinib, or pazopanib were assessed to report population differences in PFS and/or OS. For 28 (38%) of the analyses that showed suggestions of a potential efficacy difference across subpopulations, limitations in the data available precluded further assessment. There were 17 (23%) analyses assessed to report comparable efficacy outcomes across diverse subpopulations. The majority of clinical trials noted no clinically remarkable differences in safety between subpopulations; however, for brigatinib, crizotinib, pazopanib, and sunitinib, distinct patterns of adverse events were reported in the Asian and non-Asian subgroups. The underrepresentation of specific subpopulations, the grouping together of results of diverse subpopulations, as well as inconsistencies in the definition and reporting of participant ethnicity/ancestry are barriers to the meaningful exploration of inter-ethnic differences in TKI response. Therefore, further insight into the associations between ethnicity/ancestry and TKI response will require an increase in the diversity of clinical trial participants and appropriate analysis and reporting of subpopulation results.

摘要

酪氨酸激酶抑制剂(TKIs)的疗效和安全性在不同种族/血统亚组中存在差异(此前综述至2017年)。自那时以来,随着获批的TKIs数量不断增加,对3期TKI临床试验中不同种族/血统亚组的TKI反应进行了更新综述。通过文献检索,共确定了73项关于无进展生存期(PFS)和/或总生存期(OS)的人群亚组分析(根据参与者的种族、民族、血统或地理区域定义)。在调查阿法替尼、布加替尼、达可替尼、吉列替尼、劳拉替尼、奈拉替尼、奥希替尼或帕唑帕尼疗效的分析中,有12项(16%)被评估为报告了PFS和/或OS的人群差异。在28项(38%)显示亚组间可能存在疗效差异迹象的分析中,可用数据的局限性妨碍了进一步评估。有17项(23%)分析被评估为报告了不同亚组间相当的疗效结果。大多数临床试验指出亚组间在安全性方面无临床显著差异;然而,对于布加替尼、克唑替尼、帕唑帕尼和舒尼替尼,在亚洲和非亚洲亚组中报告了不同的不良事件模式。特定亚组代表性不足、不同亚组结果合并在一起,以及参与者种族/血统定义和报告的不一致,都是有意义地探索TKI反应种族间差异的障碍。因此,要进一步深入了解种族/血统与TKI反应之间的关联,需要增加临床试验参与者的多样性,并对亚组结果进行适当分析和报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3bf/12037692/4fe324367f60/CTS-18-e70224-g002.jpg

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