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Efficacy and safety of selpercatinib in Chinese patients with advanced RET-altered thyroid cancers: results from the phase II LIBRETTO-321 study

BACKGROUND: Selpercatinib, a highly selective and potent REarranged during Transfection (RET) kinase inhibitor, is effective in advanced RET-altered thyroid cancer (TC). However, the efficacy and safety in Chinese patients are unknown. PATIENTS AND METHODS: In the open-label, multi-center phase II L...

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Autores principales: Zheng, Xiangqian, Ji, Qinghai, Sun, Yuping, Ge, Minghua, Zhang, Bin, Cheng, Ying, Lei, Shangtong, Shi, Feng, Guo, Ye, Li, Linfa, Chen, Lu, Shao, Jingxin, Zhang, Wanli, Gao, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434679/
https://www.ncbi.nlm.nih.gov/pubmed/36062046
http://dx.doi.org/10.1177/17588359221119318
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author Zheng, Xiangqian
Ji, Qinghai
Sun, Yuping
Ge, Minghua
Zhang, Bin
Cheng, Ying
Lei, Shangtong
Shi, Feng
Guo, Ye
Li, Linfa
Chen, Lu
Shao, Jingxin
Zhang, Wanli
Gao, Ming
author_facet Zheng, Xiangqian
Ji, Qinghai
Sun, Yuping
Ge, Minghua
Zhang, Bin
Cheng, Ying
Lei, Shangtong
Shi, Feng
Guo, Ye
Li, Linfa
Chen, Lu
Shao, Jingxin
Zhang, Wanli
Gao, Ming
author_sort Zheng, Xiangqian
collection PubMed
description BACKGROUND: Selpercatinib, a highly selective and potent REarranged during Transfection (RET) kinase inhibitor, is effective in advanced RET-altered thyroid cancer (TC). However, the efficacy and safety in Chinese patients are unknown. PATIENTS AND METHODS: In the open-label, multi-center phase II LIBRETTO-321 (NCT04280081) study, Chinese patients with advanced solid tumors harboring RET alterations received selpercatinib 160 mg twice daily. The primary endpoint was objective response rate (ORR; RECIST v1.1) by independent review committee (IRC). Secondary endpoints included duration of response (DoR) and safety. Efficacy was assessed in the primary analysis set [PAS; treated patients with RET fusion-positive TC or RET-mutant medullary TC (MTC) confirmed by central laboratory] and all enrolled patients with MTC. RESULTS: Of 77 enrolled patients, 29 had RET-mutant MTC and one had RET fusion-positive TC. In the PAS (n = 26), the ORR by IRC was 57.7% [95% confidence interval (CI), 36.9–76.6]. Median DoR was not reached and 93.3% of responses were ongoing at a median follow-up of 8.7 months. In all enrolled MTC patients (n = 29), the ORR by IRC was 58.6% (95% CI, 38.9–76.5). One RET fusion-positive TC patient treated for 23.4 weeks achieved a partial response at week 8 that was ongoing at cutoff. In the safety population (n = 77), 59.7% experienced grade ⩾3 treatment-emergent adverse events (TEAEs). TEAEs led to dose reductions in 32.5% (n = 25) and discontinuations in 5.2% [n = 4; 3.9% (n = 3) considered treatment related] of patients. CONCLUSIONS: Selpercatinib showed robust antitumor activity and was well tolerated in Chinese patients with advanced RET-altered TC, consistent with global data from LIBRETTO-001 (NCT04280081). CLINICALTRIALS.GOV IDENTIFIER: NCT04280081 (first posted Feb 21, 2020)
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spelling pubmed-94346792022-09-02 Efficacy and safety of selpercatinib in Chinese patients with advanced RET-altered thyroid cancers: results from the phase II LIBRETTO-321 study Zheng, Xiangqian Ji, Qinghai Sun, Yuping Ge, Minghua Zhang, Bin Cheng, Ying Lei, Shangtong Shi, Feng Guo, Ye Li, Linfa Chen, Lu Shao, Jingxin Zhang, Wanli Gao, Ming Ther Adv Med Oncol Original Research BACKGROUND: Selpercatinib, a highly selective and potent REarranged during Transfection (RET) kinase inhibitor, is effective in advanced RET-altered thyroid cancer (TC). However, the efficacy and safety in Chinese patients are unknown. PATIENTS AND METHODS: In the open-label, multi-center phase II LIBRETTO-321 (NCT04280081) study, Chinese patients with advanced solid tumors harboring RET alterations received selpercatinib 160 mg twice daily. The primary endpoint was objective response rate (ORR; RECIST v1.1) by independent review committee (IRC). Secondary endpoints included duration of response (DoR) and safety. Efficacy was assessed in the primary analysis set [PAS; treated patients with RET fusion-positive TC or RET-mutant medullary TC (MTC) confirmed by central laboratory] and all enrolled patients with MTC. RESULTS: Of 77 enrolled patients, 29 had RET-mutant MTC and one had RET fusion-positive TC. In the PAS (n = 26), the ORR by IRC was 57.7% [95% confidence interval (CI), 36.9–76.6]. Median DoR was not reached and 93.3% of responses were ongoing at a median follow-up of 8.7 months. In all enrolled MTC patients (n = 29), the ORR by IRC was 58.6% (95% CI, 38.9–76.5). One RET fusion-positive TC patient treated for 23.4 weeks achieved a partial response at week 8 that was ongoing at cutoff. In the safety population (n = 77), 59.7% experienced grade ⩾3 treatment-emergent adverse events (TEAEs). TEAEs led to dose reductions in 32.5% (n = 25) and discontinuations in 5.2% [n = 4; 3.9% (n = 3) considered treatment related] of patients. CONCLUSIONS: Selpercatinib showed robust antitumor activity and was well tolerated in Chinese patients with advanced RET-altered TC, consistent with global data from LIBRETTO-001 (NCT04280081). CLINICALTRIALS.GOV IDENTIFIER: NCT04280081 (first posted Feb 21, 2020) SAGE Publications 2022-08-29 /pmc/articles/PMC9434679/ /pubmed/36062046 http://dx.doi.org/10.1177/17588359221119318 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Zheng, Xiangqian
Ji, Qinghai
Sun, Yuping
Ge, Minghua
Zhang, Bin
Cheng, Ying
Lei, Shangtong
Shi, Feng
Guo, Ye
Li, Linfa
Chen, Lu
Shao, Jingxin
Zhang, Wanli
Gao, Ming
Efficacy and safety of selpercatinib in Chinese patients with advanced RET-altered thyroid cancers: results from the phase II LIBRETTO-321 study
title Efficacy and safety of selpercatinib in Chinese patients with advanced RET-altered thyroid cancers: results from the phase II LIBRETTO-321 study
title_full Efficacy and safety of selpercatinib in Chinese patients with advanced RET-altered thyroid cancers: results from the phase II LIBRETTO-321 study
title_fullStr Efficacy and safety of selpercatinib in Chinese patients with advanced RET-altered thyroid cancers: results from the phase II LIBRETTO-321 study
title_full_unstemmed Efficacy and safety of selpercatinib in Chinese patients with advanced RET-altered thyroid cancers: results from the phase II LIBRETTO-321 study
title_short Efficacy and safety of selpercatinib in Chinese patients with advanced RET-altered thyroid cancers: results from the phase II LIBRETTO-321 study
title_sort efficacy and safety of selpercatinib in chinese patients with advanced ret-altered thyroid cancers: results from the phase ii libretto-321 study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434679/
https://www.ncbi.nlm.nih.gov/pubmed/36062046
http://dx.doi.org/10.1177/17588359221119318
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