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Patient-Reported Outcomes with Selpercatinib Treatment Among Patients with RET-Mutant Medullary Thyroid Cancer in the Phase I/II LIBRETTO-001 Trial.
Wirth, Lori J; Robinson, Bruce; Boni, Valentina; Tan, Daniel S W; McCoach, Caroline; Massarelli, Erminia; Hess, Lisa M; Jen, Min-Hua; Kherani, Jennifer; Olek, Elizabeth; Subbiah, Vivek.
Afiliación
  • Wirth LJ; Massachusetts General Hospital, Boston, MA, USA.
  • Robinson B; Royal North Shore Hospital, Sydney, Australia.
  • Boni V; START Madrid-Centro Integral Oncológico Clara Campal (CIOCC), Hm Hospitales Sanchinarro, Madrid, Spain.
  • Tan DSW; National Cancer Centre Singapore, Singapore.
  • McCoach C; University of California at San Francisco, CA, USA.
  • Massarelli E; City of Hope, Duarte, CA, USA.
  • Hess LM; Eli Lilly & Co., Indianapolis, IN, USA.
  • Jen MH; Eli Lilly & Co., Indianapolis, IN, USA.
  • Kherani J; Loxo Oncology, a wholly owned subsidiary of Eli Lilly & Co., Stamford, CT, USA.
  • Olek E; Loxo Oncology, a wholly owned subsidiary of Eli Lilly & Co., Stamford, CT, USA.
  • Subbiah V; The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Oncologist ; 27(1): 13-21, 2022 02 03.
Article en En | MEDLINE | ID: mdl-34516023
BACKGROUND: 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. MATERIALS AND METHODS: 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). RESULTS: 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. CONCLUSION: 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Tiroides / Carcinoma Neuroendocrino Límite: Humans Idioma: En Revista: Oncologist Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Tiroides / Carcinoma Neuroendocrino Límite: Humans Idioma: En Revista: Oncologist Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos