Massachusetts General Hospital, Boston, MA, USA.
Royal North Shore Hospital, Sydney, Australia.
Oncologist. 2022 Feb 3;27(1):13-21. doi: 10.1002/onco.13977.
Medullary thyroid cancer (MTC) standard of care includes multikinase inhibitors (MKIs), which can exacerbate disease-related diarrhea, primarily because of non-RET kinase inhibition. We report diarrhea and other patient-reported outcomes (PROs) with selpercatinib, a highly selective RET inhibitor, among patients with RET-mutant MTC in the ongoing, phase I/II LIBRETTO-001 trial.
Instrument completion time points were baseline (cycle 1, day 1) and approximately every other 28-day cycle until cycle 13 (every 12 weeks thereafter) for the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30, and baseline, weekly during cycle 1, and day 1 of every cycle for the modified Systemic Therapy-Induced Diarrhea Assessment Tool (mSTIDAT). A ≥10-point change from baseline in domain score was considered clinically meaningful. PROs were summarized through cycle 13 in all patients and by subgroups with or without prior exposure to MKIs vandetanib and/or cabozantinib (V/C).
Among the overall MTC population (n = 226), 88 (39%) and 124 (55%) patients comprised the V/C-naïve and previous V/C subgroups, respectively. Compliance was >85% for both instruments at each time point. Most patients maintained/improved in all health-related quality of life (HRQoL) subscales throughout treatment. Improvements in diarrhea were clinically meaningful in 43.5% of patients overall and in 36.8% and 51.3% of V/C-naïve and previous V/C subgroups, respectively. At baseline, 80.4% of all patients reported diarrhea on mSTIDAT. The percentage of patients who reported diarrhea was reduced to less than half of all patients (range: 33.3%-48.3%) after cycle 2.
These interim results demonstrate that patients with RET-mutant MTC improved/remained stable on all domains of HRQoL during treatment with selpercatinib. Future analyses will be conducted as the data mature.
甲状腺髓样癌(MTC)的标准治疗包括多激酶抑制剂(MKIs),这些药物可能会加重与疾病相关的腹泻,主要是因为非 RET 激酶抑制。我们报告了在正在进行的 I/II 期 LIBRETTO-001 试验中,RET 突变型 MTC 患者使用高度选择性 RET 抑制剂塞尔帕替尼(selpercatinib)后的腹泻和其他患者报告的结局(PRO)。
欧洲癌症研究和治疗组织生活质量问卷核心 30 量表的仪器完成时间点为基线(第 1 周期,第 1 天)和大约每 28 天的周期,直到第 13 周期(此后每 12 周);改良的系统治疗诱导性腹泻评估工具(mSTIDAT)在第 1 周期期间每周一次,以及每个周期的第 1 天。从基线开始,域评分至少增加 10 分被认为具有临床意义。在所有患者以及先前暴露于 MKI 凡德他尼(vandetanib)和/或卡博替尼(cabozantinib)(V/C)的患者亚组中,通过第 13 周期总结了 PRO。
在整个 MTC 人群中(n=226),88 名(39%)和 124 名(55%)患者分别构成了 V/C 初治和先前 V/C 亚组。在每个时间点,两种仪器的依从性均>85%。在整个治疗过程中,大多数患者在所有健康相关生活质量(HRQoL)亚量表中保持/改善。整体而言,43.5%的患者腹泻得到了临床意义上的改善,V/C 初治和先前 V/C 亚组分别为 36.8%和 51.3%。在基线时,所有患者中有 80.4%在 mSTIDAT 上报告了腹泻。在第 2 周期后,报告腹泻的患者比例降低至不到所有患者的一半(范围:33.3%-48.3%)。
这些中期结果表明,在接受塞尔帕替尼治疗期间,RET 突变型 MTC 患者在所有 HRQoL 领域均得到改善/稳定。随着数据的成熟,未来将进行进一步分析。