Case Report: Successful late-line pralsetinib treatment in an ALK-rearranged lung adenocarcinoma patient with KIF5B-RET fusion resistant to alectinib.

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY
Frontiers in Genetics Pub Date : 2025-06-17 eCollection Date: 2025-01-01 DOI:10.3389/fgene.2025.1569912
Feng Jin, Chenyang Wang, Fang Yang, Shubin Wang, Fen Wang
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Abstract

Anaplastic lymphoma kinase (ALK) fusion, an oncogenic driver alteration, accounts for 5%-6% of non-small cell lung cancer (NSCLC) patients. ALK tyrosine kinase inhibitors (TKIs) provide significant clinical benefit in advanced ALK-rearranged NSCLC. However, acquired resistance to ALK TKIs inevitably arises, and the underlying mechanisms remain incompletely elucidated. This report describes a stage IV lung adenocarcinoma (LUAD) patient with ALK-rearranged who developed KIF5B-RET fusion-mediated resistance following second-line alectinib therapy. The patient achieved a partial response (PR) to third-line pralsetinib, sustained for 4 months. This case highlights KIF5B-RET fusion as a potential resistance mechanism post alectinib treatment and suggested = pralsetinib, a RET inhibitor, as a viable therapeutic option in this context. These findings contribute to the evolving understanding of resistance management strategies in ALK-rearranged NSCLC.

病例报告:alk重排的肺腺癌患者,KIF5B-RET融合对阿勒替尼耐药,晚期普莱替尼治疗成功。
间变性淋巴瘤激酶(ALK)融合是一种致癌驱动改变,占非小细胞肺癌(NSCLC)患者的5%-6%。ALK酪氨酸激酶抑制剂(TKIs)为晚期ALK重排NSCLC提供了显著的临床益处。然而,对ALK TKIs的获得性耐药不可避免地出现,其潜在机制尚未完全阐明。本报告描述了一名alk重排的IV期肺腺癌(LUAD)患者在二线阿勒替尼治疗后出现KIF5B-RET融合介导的耐药。患者对三线普拉塞替尼达到部分缓解(PR),持续4个月。该病例强调了KIF5B-RET融合是阿勒替尼治疗后的潜在耐药机制,并建议在这种情况下,RET抑制剂普拉塞替尼作为可行的治疗选择。这些发现有助于对alk重排非小细胞肺癌耐药管理策略的不断发展理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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