拉罗特雷克提尼布在患有NTRK融合瘤的患者中:来自NCI-MATCH ECOG-ACRIN试验 (EAY131) 副协议EAY131-Z1EE1的结果
Neal Akhave1, Zihe Song2, David S Hong1
1The University of Texas MD Anderson Cancer Center, Houston, TX.
JCO precision oncology
|February 20, 2026
概括
拉罗特雷克提尼布在治疗神经营性热氨酸受体激酶 (NTRK) 融合阳性癌症方面表现出显著的疗效,显示出高客观反应率和有利的安全性. 这支持其在精密医学中用于NTRK驱动的瘤的应用.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 基因组学就是基因组学.
- 精准医学是一门精准的医学.
背景情况:
- 神经断性热胺受体激酶 (NTRK) 基因融合是各种人类癌症的致癌驱动因素.
- 识别和准这些融合对于有效的癌症治疗至关重要.
- 拉罗特雷克提尼布是所有三种TRK蛋白 (TRKA,TRKB,TRKC) 的选择性抑制剂.
研究的目的:
- 为了研究larotrectinib在患有NTRK融合阳性癌症的患者中的疗效和安全性.
- 为了评估larotrectinib在NCI-MATCH (治疗选择分子分析) 试验中的表现,Z1E子协议.
主要方法:
- 在NCI-MATCH分协议Z1E中,纳入了具有NTRK融合的固体瘤或淋巴瘤的患者.
- 患者每天两次服用larotrectinib 100 mg,直到疾病进展或毒性.
- 主要终点是客观应答率 (ORR);次要终点包括无进展生存率 (PFS) 和整体生存率 (OS).
主要成果:
- 在六种组织学中,12名NTRK融合阳性瘤患者接受了larotrectinib.
- 客观反应率 (ORR) 为75%,中位数PFS为14.4个月,中位数OS为23.9个月.
- 治疗耐受性良好,主要有1级不良事件.
结论:
- 拉罗特雷克提尼布在NTRK融合阳性瘤中提供了显著的临床益处和明显的ORR.
- 该药物表现出良好的安全性,支持其组织无关的批准.
- 包括NTRK1,NTRK2和NTRK3在内的综合分子测试对于识别可以从larotrectinib中受益的患者至关重要.
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