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Efficacy, safety and dose selection of AZD3759 in patients with untreated EGFR-mutated non-small-cell lung cancer and central nervous system metastases in China (CTONG1702-Arm 8): a multi-center, single-arm, phase 2 trial
BACKGROUND: Central nervous system (CNS) metastases is inevitable for epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC). AZD3759 is a novel EGFR-TKI with impressive CNS penetration. METHODS: We initiated a phase 2, multi-center, umbrella trial (CTONG1702, NCT03574402)...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541475/ https://www.ncbi.nlm.nih.gov/pubmed/37781161 http://dx.doi.org/10.1016/j.eclinm.2023.102238 |
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author | Maggie Liu, Si-Yang Dong, Xiao-Rong Wang, Zhen Du, Yingying Cui, Jiu-Wei Chu, Qian Xu, Bing-Fei Zheng, Ming-Ying Deng, Jia-Yi Lu, Chang Wei, Xue-Wu Li, Yang-Si Zheng, Mei-Mei Yang, Ming-Yi Huang, Jie Li, Anna Bai, Xiao-Yan Sun, Yue-Li Xu, Chong-Rui Wang, Bin-Chao Chen, Hua-Jun Yang, Jin-Ji Yan, Hong-Hong Zhong, Wen-Zhao Zhou, Qing Wu, Yi-Long |
author_facet | Maggie Liu, Si-Yang Dong, Xiao-Rong Wang, Zhen Du, Yingying Cui, Jiu-Wei Chu, Qian Xu, Bing-Fei Zheng, Ming-Ying Deng, Jia-Yi Lu, Chang Wei, Xue-Wu Li, Yang-Si Zheng, Mei-Mei Yang, Ming-Yi Huang, Jie Li, Anna Bai, Xiao-Yan Sun, Yue-Li Xu, Chong-Rui Wang, Bin-Chao Chen, Hua-Jun Yang, Jin-Ji Yan, Hong-Hong Zhong, Wen-Zhao Zhou, Qing Wu, Yi-Long |
author_sort | Maggie Liu, Si-Yang |
collection | PubMed |
description | BACKGROUND: Central nervous system (CNS) metastases is inevitable for epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC). AZD3759 is a novel EGFR-TKI with impressive CNS penetration. METHODS: We initiated a phase 2, multi-center, umbrella trial (CTONG1702, NCT03574402). The eighth arm assessed the efficacy and safety of AZD3759 in untreated EGFR-mutated NSCLC with CNS metastases. The primary objective was the objective response rate (ORR). Simon’s minimax two-stage design was used to calculate the sample size. Dose optimal selection was performed using 200- and 300-mg bid cohorts. FINDINGS: Between Oct 18, 2018 and Sep 14, 2020, 30 patients received AZD3759 at 200 mg (n = 15) or 300 mg (n = 15) bid. At data cutoff (Dec 31, 2022), median follow-up was 35.4 months. The primary endpoint was reached, with a confirmed ORR of 70% (21/30) (200 mg, 80%; 300 mg, 60%). The median progression-free survival was 12.9 months (200 mg, 15.8 months; 300 mg, 10.7 months). Grade 3 or 4 treatment-related adverse events occurred in 73% (22/30) of the patients (200 mg: 60%; 300 mg: 87%). 59% (10/17) of the patients developed a T790M mutation at disease progression. The median overall survival was 33.7 months, and 34.1 months and 25.3 months in patient treated with or without osimertinib in a later-line setting, respectively. INTERPRETATION: AZD3759 showed promising efficacy and tolerable safety as a first-line therapy in EGFR-mutated NSCLC with CNS metastases. The 200-mg bid cohort had better clinical outcomes. Sequential use of AZD3759 and third-generation EGFR-TKIs represents a new option. FUNDING: Chinese Thoracic Oncology Group (CTONG). |
format | Online Article Text |
id | pubmed-10541475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105414752023-10-01 Efficacy, safety and dose selection of AZD3759 in patients with untreated EGFR-mutated non-small-cell lung cancer and central nervous system metastases in China (CTONG1702-Arm 8): a multi-center, single-arm, phase 2 trial Maggie Liu, Si-Yang Dong, Xiao-Rong Wang, Zhen Du, Yingying Cui, Jiu-Wei Chu, Qian Xu, Bing-Fei Zheng, Ming-Ying Deng, Jia-Yi Lu, Chang Wei, Xue-Wu Li, Yang-Si Zheng, Mei-Mei Yang, Ming-Yi Huang, Jie Li, Anna Bai, Xiao-Yan Sun, Yue-Li Xu, Chong-Rui Wang, Bin-Chao Chen, Hua-Jun Yang, Jin-Ji Yan, Hong-Hong Zhong, Wen-Zhao Zhou, Qing Wu, Yi-Long eClinicalMedicine Articles BACKGROUND: Central nervous system (CNS) metastases is inevitable for epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC). AZD3759 is a novel EGFR-TKI with impressive CNS penetration. METHODS: We initiated a phase 2, multi-center, umbrella trial (CTONG1702, NCT03574402). The eighth arm assessed the efficacy and safety of AZD3759 in untreated EGFR-mutated NSCLC with CNS metastases. The primary objective was the objective response rate (ORR). Simon’s minimax two-stage design was used to calculate the sample size. Dose optimal selection was performed using 200- and 300-mg bid cohorts. FINDINGS: Between Oct 18, 2018 and Sep 14, 2020, 30 patients received AZD3759 at 200 mg (n = 15) or 300 mg (n = 15) bid. At data cutoff (Dec 31, 2022), median follow-up was 35.4 months. The primary endpoint was reached, with a confirmed ORR of 70% (21/30) (200 mg, 80%; 300 mg, 60%). The median progression-free survival was 12.9 months (200 mg, 15.8 months; 300 mg, 10.7 months). Grade 3 or 4 treatment-related adverse events occurred in 73% (22/30) of the patients (200 mg: 60%; 300 mg: 87%). 59% (10/17) of the patients developed a T790M mutation at disease progression. The median overall survival was 33.7 months, and 34.1 months and 25.3 months in patient treated with or without osimertinib in a later-line setting, respectively. INTERPRETATION: AZD3759 showed promising efficacy and tolerable safety as a first-line therapy in EGFR-mutated NSCLC with CNS metastases. The 200-mg bid cohort had better clinical outcomes. Sequential use of AZD3759 and third-generation EGFR-TKIs represents a new option. FUNDING: Chinese Thoracic Oncology Group (CTONG). Elsevier 2023-09-22 /pmc/articles/PMC10541475/ /pubmed/37781161 http://dx.doi.org/10.1016/j.eclinm.2023.102238 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Articles Maggie Liu, Si-Yang Dong, Xiao-Rong Wang, Zhen Du, Yingying Cui, Jiu-Wei Chu, Qian Xu, Bing-Fei Zheng, Ming-Ying Deng, Jia-Yi Lu, Chang Wei, Xue-Wu Li, Yang-Si Zheng, Mei-Mei Yang, Ming-Yi Huang, Jie Li, Anna Bai, Xiao-Yan Sun, Yue-Li Xu, Chong-Rui Wang, Bin-Chao Chen, Hua-Jun Yang, Jin-Ji Yan, Hong-Hong Zhong, Wen-Zhao Zhou, Qing Wu, Yi-Long Efficacy, safety and dose selection of AZD3759 in patients with untreated EGFR-mutated non-small-cell lung cancer and central nervous system metastases in China (CTONG1702-Arm 8): a multi-center, single-arm, phase 2 trial |
title | Efficacy, safety and dose selection of AZD3759 in patients with untreated EGFR-mutated non-small-cell lung cancer and central nervous system metastases in China (CTONG1702-Arm 8): a multi-center, single-arm, phase 2 trial |
title_full | Efficacy, safety and dose selection of AZD3759 in patients with untreated EGFR-mutated non-small-cell lung cancer and central nervous system metastases in China (CTONG1702-Arm 8): a multi-center, single-arm, phase 2 trial |
title_fullStr | Efficacy, safety and dose selection of AZD3759 in patients with untreated EGFR-mutated non-small-cell lung cancer and central nervous system metastases in China (CTONG1702-Arm 8): a multi-center, single-arm, phase 2 trial |
title_full_unstemmed | Efficacy, safety and dose selection of AZD3759 in patients with untreated EGFR-mutated non-small-cell lung cancer and central nervous system metastases in China (CTONG1702-Arm 8): a multi-center, single-arm, phase 2 trial |
title_short | Efficacy, safety and dose selection of AZD3759 in patients with untreated EGFR-mutated non-small-cell lung cancer and central nervous system metastases in China (CTONG1702-Arm 8): a multi-center, single-arm, phase 2 trial |
title_sort | efficacy, safety and dose selection of azd3759 in patients with untreated egfr-mutated non-small-cell lung cancer and central nervous system metastases in china (ctong1702-arm 8): a multi-center, single-arm, phase 2 trial |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541475/ https://www.ncbi.nlm.nih.gov/pubmed/37781161 http://dx.doi.org/10.1016/j.eclinm.2023.102238 |
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