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Phase III study of HR-positive/HER2-negative/lymph node-positive breast cancer non-responsive to primary chemotherapy: a randomized trial.
Yang, Yang; He, Yingjian; Fan, Zhaoqing; Chen, Xue; Liu, Yiqiang; Zhang, Chao; Jiang, Hongchuan; Wang, Xin; Wang, Xiang; Xie, Fei; Wang, Shu; Luo, Bin; Kang, Hua; Wang, Tao; Jiang, Zefei; Yuan, Peng; Xu, Binhe; Xu, Ling; Liu, Yinhua; Li, Jinfeng; Xie, Yuntao; Wang, Tianfeng; Ouyang, Tao.
Afiliação
  • Yang Y; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China.
  • He Y; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China.
  • Fan Z; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China. zhqfan@bjmu.edu.cn.
  • Chen X; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China.
  • Liu Y; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China.
  • Zhang C; Beijing Chao Yang Hospital, Breast Disease Department, Beijing, China.
  • Jiang H; Beijing Chao Yang Hospital, Breast Disease Department, Beijing, China.
  • Wang X; Cancer Hospital, Chinese Academy of Medical Sciences, Breast Cancer Department, Beijing, China.
  • Wang X; Cancer Hospital, Chinese Academy of Medical Sciences, Breast Cancer Department, Beijing, China.
  • Xie F; Peking University People's Hospital, Breast Cancer Center, Beijing, China.
  • Wang S; Peking University People's Hospital, Breast Cancer Center, Beijing, China.
  • Luo B; Beijing Tsinghua Changgeng Hospital, Breast Disease Department, Beijing, China.
  • Kang H; Xuan Wu Hospital Capital Medical University, Breast Disease Department, Beijing, China.
  • Wang T; 307 Hospital of PLA, Breast Cancer Department, Beijing, China.
  • Jiang Z; 307 Hospital of PLA, Breast Cancer Department, Beijing, China.
  • Yuan P; Cancer Hospital, Chinese Academy of Medical Sciences, Breast Cancer Department, Beijing, China.
  • Xu B; Cancer Hospital, Chinese Academy of Medical Sciences, Breast Cancer Department, Beijing, China.
  • Xu L; Peking University First Hospital, Breast Cancer Center, Beijing, China.
  • Liu Y; Peking University First Hospital, Breast Cancer Center, Beijing, China.
  • Li J; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China.
  • Xie Y; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China.
  • Wang T; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China.
  • Ouyang T; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Breast Center, Peking University Cancer Hospital & Institute, Beijing, China.
NPJ Breast Cancer ; 9(1): 54, 2023 Jun 21.
Article em En | MEDLINE | ID: mdl-37344451
There are few studies focus on post-neoadjuvant treatment in hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-)/lymph node-positive (LN+) breast cancer, a multi-center, open-label, randomized, controlled phase III trial was conducted to evaluate pathological response-guided non-cross-resistant adjuvant chemotherapy in patients with HR+/HER2-/LN+ breast cancer who were non-responsive to primary chemotherapy. Patients received four cycles of non-cross-resistant adjuvant chemotherapy plus endocrine therapy (ET), or ET alone. Forty patients responsive to neoadjuvant chemotherapy and with Miller and Payne G4 or G5 and LN- status were assigned to the observation group. Distant disease-free survival was the primary endpoint. The final intention-to-treat analysis comprised 379 patients. After a median follow-up period of 72.4 months, the 5-year distant disease-free survival was 92% and 90% in the chemotherapy plus ET and ET-alone groups, respectively. Comparatively, the observation group showed a trend towards better distant disease-free survival. For patients non-responsive to neoadjuvant chemotherapy, adjuvant non-cross-resistant chemotherapy did not significantly improve distant disease-free survival compared to ET alone.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: NPJ Breast Cancer Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: NPJ Breast Cancer Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China
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