EGFR突变非小细胞肺癌患者使用EGFR- tki前后T790M等位基因频率与治疗效果的关系

Cancer diagnosis & prognosis Pub Date : 2025-05-03 eCollection Date: 2025-05-01 DOI:10.21873/cdp.10441
Koichi Ogawa, Hiroyasu Kaneda, Yasuhiro Koh, Yoshiya Matsumoto, Kenji Sawa, Motohiro Tamiya, Nobuhisa Ishikawa, Kenichi Minami, Hidekazu Suzuki, Yosuke Eguchi, Masaki Kanazu, Yuki Sato, Tomoya Kawaguchi
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摘要

背景/目的:本研究旨在通过阐明治疗效果与EGFR T790M突变等位基因频率的相关性,探讨阿法替尼和奥西替尼序贯治疗的有效性。患者与方法:2013年8月至2019年7月,收集8家机构患者表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)给药前后的肿瘤样本。我们利用主要接受阿法替尼治疗的患者的活检标本,采用液滴数字聚合酶链反应测量了T790M突变等位基因频率,并分析了活检前后组织中T790M与egfr激活的突变比率(T/A比率)。结果:36例保存活检前后组织的患者(阿法替尼组24例,第一代EGFR-TKI组12例)中,阿法替尼组给药前(T/A前)和给药后(T/A后)的中位T/A比分别为0.005和0.014,第一代EGFR-TKI组分别为0.026和0.352。Mann-Whitney u检验结果显示,与第一代EGFR-TKI相比,阿法替尼组pre-T/ a和post-T/ a比率的差异并不高(p=0.0372)。两组间无进展生存期或总生存期无显著差异。结论:与第一代EGFR-TKI治疗相比,阿法替尼治疗不影响T/A比值的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relationship Between T790M Allele Frequency and Therapeutic Effects Before and After EGFR-TKI Administration Using Droplet Digital PCR in Non-small-cell Lung Cancer With EGFR Mutation.

Background/aim: This study aimed to investigate the effectiveness of sequential treatment with afatinib and osimertinib by clarifying the correlation between therapeutic effects and EGFR T790M mutant allele frequency.

Patients and methods: From August 2013 to July 2019, tumor samples from before and after epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) administration were collected from patients from eight institutions. We measured T790M mutant allele frequency using droplet digital polymerase chain reaction using biopsy specimens from patients mainly treated with afatinib and analyzed the T790M to EGFR-activating mutation ratio (T/A ratio) in pre- and post-biopsy tissue.

Results: Among 36 patients (afatinib group: n=24, first-generation EGFR-TKI group: n=12) with preserved pre- and post-biopsy tissue, the median T/A ratios before (pre-T/A ratio) and after EGFR-TKI administration (post-T/A ratio) in the afatinib group were 0.005 and 0.014, and those in the first-generation EGFR-TKI group were 0.026 and 0.352, respectively. The results of a Mann-Whitney U-test revealed that the difference between the pre-T/A and post-T/A ratios was not higher in the afatinib group than in the first-generation EGFR-TKI (p=0.0372). No significant difference in progression-free or overall survival was found between the two groups.

Conclusion: Compared with first-generation EGFR-TKI treatment, treatment with afatinib did not affect changes in the T/A ratio.

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