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非小细胞肺癌中罕见致癌驱动因素的新策略:2024年欧洲肿瘤内科学会年会最新进展

Novel strategies for rare oncogenic drivers in non-small-cell lung cancer: An update from the 2024 Annual ESMO meeting.

作者信息

van der Wel J W T, de Langen A J

机构信息

Netherlands Cancer Institute, Department of Thoracic Oncology, Amsterdam, The Netherlands.

Netherlands Cancer Institute, Department of Thoracic Oncology, Amsterdam, The Netherlands.

出版信息

Lung Cancer. 2025 Jun;204:108490. doi: 10.1016/j.lungcan.2025.108490. Epub 2025 Mar 14.

Abstract

Across the landscape of oncogene-addicted non-small-cell lung cancer (NSCLC), various tyrosine kinase inhibitors (TKIs) have been introduced in the last twenty years. During the 2024 Annual ESMO meeting new therapeutic options were presented for EGFR exon 20 insertion mutation, ALK fusion and ROS1 fusion positive advanced stage NSCLC. For EGFR exon 20 insertion mutation positive NSCLC, results from REZILIENT-1, a single arm phase II study with zipalertinib, were presented, showing an objective response rate (ORR) of 50% in patients that were pretreated with amivantamab, and 25% in patients pretreated with amivantamab and an EGFR exon 20 insertion-directed TKI. The vast majority of these patients also received platinum-doublet chemotherapy. For ALK, results from ALKOVE-1, a single arm phase I/II study with NVL-655, a next generation ALK TKI, were presented. The ORR was 35 % in patients pretreated with ≥ 2 ALK TKIs including lorlatinib and 57 % in patients pretreated with ≥ 1 ALK TKI, excluding lorlatinib. The median number of prior anticancer therapies was 3. Intracranial responses were seen in lorlatinib naïve- and lorlatinib pretreated patients and toxicity was manageable. In addition, results of the first-line randomized phase III INSPIRE study were presented, in which iruplinalkib, an ALK and ROS1 selective TKI, is being evaluated versus crizotinib. Iruplinalkib showed a superior median PFS (36.8 versus 14.55 months for crizotinib), but no difference in 36-month overall survival (OS) rate. Finally, results from ARROS-1, a single arm phase I/II study with zidesamtinib, a ROS1 selective and TRK-sparing TKI, were presented. An ORR of 73% was obtained in patients that were pretreated with crizotinib and an ORR of 38% in patients pretreated with repotrectinib. In this review, we will discuss the relevant study results presented at ESMO 2024 for these three genomic drivers and hypothesize on their respective place in the sequence of treatment options.

摘要

在成瘾性致癌基因的非小细胞肺癌(NSCLC)领域,过去二十年来已引入了各种酪氨酸激酶抑制剂(TKI)。在2024年欧洲肿瘤内科学会(ESMO)年度会议上,针对表皮生长因子受体(EGFR)外显子20插入突变、间变性淋巴瘤激酶(ALK)融合和ROS1融合阳性的晚期NSCLC提出了新的治疗选择。对于EGFR外显子20插入突变阳性的NSCLC,公布了REZILIENT - 1的结果,这是一项使用齐帕替尼的单臂II期研究,结果显示,接受阿美替尼预处理的患者客观缓解率(ORR)为50%,接受阿美替尼和EGFR外显子20插入定向TKI预处理的患者客观缓解率为25%。这些患者中的绝大多数还接受了铂类双联化疗。对于ALK,公布了ALKOVE - 1的结果,这是一项使用下一代ALK TKI NVL - 655的单臂I/II期研究。在接受≥2种ALK TKI(包括洛拉替尼)预处理的患者中,ORR为35%,在接受≥1种ALK TKI(不包括洛拉替尼)预处理的患者中,ORR为57%。既往抗癌治疗的中位数为3次。在未使用过洛拉替尼和使用过洛拉替尼预处理的患者中均观察到颅内反应,且毒性可控。此外,还公布了一线随机III期INSPIRE研究的结果,该研究正在评估ALK和ROS1选择性TKI艾乐替尼与克唑替尼的疗效对比。艾乐替尼显示出更长的中位无进展生存期(PFS)(36.8个月,而克唑替尼为14.55个月),但36个月总生存期(OS)率无差异。最后,公布了ARROS - 1的结果,这是一项使用ROS1选择性且保留TRK的TKI齐德替尼的单臂I/II期研究。接受克唑替尼预处理的患者ORR为73%,接受瑞波替尼预处理的患者ORR为38%。在本综述中,我们将讨论在2024年ESMO会议上公布的针对这三种基因组驱动因素的相关研究结果,并推测它们在治疗方案序列中的各自位置。

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