Stanford Cancer Institute, Stanford University, Palo Alto, CA.
Vanderbilt University Medical Center, Nashville, TN.
Curr Probl Cancer. 2021 Dec;45(6):100734. doi: 10.1016/j.currproblcancer.2021.100734. Epub 2021 Apr 2.
Neurotrophic tyrosine receptor kinase (NTRK) gene fusions lead to chimeric tropomyosin receptor kinase (TRK) fusion proteins, which act as primary oncogenic drivers in diverse tumor types in adults and children. Larotrectinib, a highly selective and central nervous system-active TRK inhibitor, has shown high objective response rates, durable disease control, and a favorable safety profile in patients with TRK fusion cancer. The impact of larotrectinib on health-related quality of life (HRQoL) was evaluated in adult and pediatric patients in two phase I/II clinical trials (NAVIGATE; NCT02576431 and SCOUT; NCT02637687). Patients completed HRQoL questionnaires (EORTC QLQ-C30, EQ-5D-5L, and PedsQL) at baseline and at planned treatment cycle visits. Changes in questionnaire scores were evaluated over time, and by tumor type and treatment response. Questionnaires from 40 adult and 17 pediatric (2-19 years of age) patients receiving larotrectinib were completed at baseline and at least one post-baseline timepoint. Meaningful within-patient HRQoL improvements occurred at one or more timepoints in 60% of adults and 76% of pediatric patients. Sustained improvements in EORTC QLQ-C30 and PedsQL scores were rapid, occurring within 2 months of treatment initiation in 68% and 71% of patients, respectively. Improvements were observed regardless of tumor type and appeared to correlate with clinical efficacy. The rapid within-patient HRQoL improvements in adult and pediatric patients with TRK fusion cancer are consistent with the clinical profile of larotrectinib. Our results provide valuable information for use of this agent in this patient population. A plain language summary of this article is available in the supplementary appendix.
神经酪氨酸受体激酶 (NTRK) 基因融合导致嵌合原肌球蛋白受体激酶 (TRK) 融合蛋白,这些蛋白在成人和儿童的多种肿瘤类型中充当主要致癌驱动因子。拉罗替尼是一种高度选择性且作用于中枢神经系统的 TRK 抑制剂,在携带 TRK 融合癌的患者中显示出较高的客观缓解率、持久的疾病控制和良好的安全性。在两项 I/II 期临床试验(NAVIGATE;NCT02576431 和 SCOUT;NCT02637687)中,评估了拉罗替尼对成年和儿科患者的健康相关生活质量(HRQoL)的影响。患者在基线和计划的治疗周期访视时完成 HRQoL 问卷(EORTC QLQ-C30、EQ-5D-5L 和 PedsQL)。随着时间的推移,按肿瘤类型和治疗反应评估问卷评分的变化。接受拉罗替尼治疗的 40 名成年和 17 名儿科(2-19 岁)患者的问卷在基线和至少一个基线后时间点完成。60%的成年患者和 76%的儿科患者在一个或多个时间点出现有意义的患者内 HRQoL 改善。EORTC QLQ-C30 和 PedsQL 评分的持续改善迅速,分别在 68%和 71%的患者中在治疗开始后 2 个月内发生。无论肿瘤类型如何,都观察到改善,并且似乎与临床疗效相关。TRK 融合癌成年和儿科患者的快速患者内 HRQoL 改善与拉罗替尼的临床特征一致。我们的结果为该药物在该患者人群中的应用提供了有价值的信息。本文的通俗易懂摘要可在补充附录中找到。