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Camrelizumab plus oxaliplatin-based chemotherapy as first-line therapy for advanced biliary tract cancer: A multicenter, phase 2 trial.
Chen, Xinni; Qin, Shukui; Gu, Shanzhi; Ren, Zhenggang; Chen, Zhendong; Xiong, Jianping; Liu, Ying; Meng, Zhiqiang; Zhang, Xiao; Wang, Linna; Zhang, Xiaojing; Zou, Jianjun.
Afiliación
  • Chen X; Department of Medical Oncology Center, Bayi Affiliated Hospital, Nanjing University of Chinese Medicine, Nanjing, China.
  • Qin S; Department of Medical Oncology Center, Bayi Affiliated Hospital, Nanjing University of Chinese Medicine, Nanjing, China.
  • Gu S; Department of Interventional Radiology, Hunan Cancer Hospital, Changsha, China.
  • Ren Z; Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Chen Z; Department of Medical Oncology, The Second Hospital of Anhui Medical University, Hefei, China.
  • Xiong J; Department of Medical Oncology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
  • Liu Y; Department of Medical Oncology, Henan Cancer Hospital, Zhengzhou, China.
  • Meng Z; Minimally Invasive Therapy Center, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Zhang X; Jiangsu Hengrui Pharmaceuticals Co., Ltd, Shanghai, China.
  • Wang L; Jiangsu Hengrui Pharmaceuticals Co., Ltd, Shanghai, China.
  • Zhang X; Jiangsu Hengrui Pharmaceuticals Co., Ltd, Shanghai, China.
  • Zou J; Jiangsu Hengrui Pharmaceuticals Co., Ltd, Shanghai, China.
Int J Cancer ; 149(11): 1944-1954, 2021 12 01.
Article en En | MEDLINE | ID: mdl-34309846
Biliary tract cancer (BTC) is a highly malignant tumor with limited treatment options and poor prognosis. Our study aimed to evaluate camrelizumab plus oxaliplatin-based chemotherapy as first-line therapy for advanced BTC. In this multicenter, open-label, phase 2 trial conducted in China (ClinicalTrials.gov, NCT03092895), untreated patients with advanced BTC were given camrelizumab (3 mg/kg iv drip injection, every 2 weeks) plus typical FOLFOX4 (Cam-FOLFOX4 group; infusional 5-fluorouracil, leucovorin and oxaliplatin) or GEMOX (Cam-GEMOX group; infusional gemcitabine and oxaliplatin). The primary endpoint was objective response rate (ORR). Ninety-two patients were enrolled: 29 received Cam-FOLFOX4 and 63 received Cam-GEMOX. The confirmed ORR and disease control rate were 16.3% (95% confidence interval [CI] = 9.4-25.5) and 75.0% (95% CI = 64.9-83.4), respectively. Median duration of response was 8.7 months (95% CI = 5.1-not reached). Median progression-free survival and overall survival were 5.3 months (95% CI = 3.7-5.7) and 12.4 months (95% CI = 8.9-16.1), respectively. Grade ≥3 treatment-related adverse events (TRAEs) occurred in 82.8% of patients receiving Cam-FOLFOX4 and in 68.3% receiving Cam-GEMOX, with no unexpected effects observed. Six (6.5%) patients discontinued treatment due to TRAE. Camrelizumab plus FOLFOX4 or GEMOX as first-line treatment was effective and tolerable for Chinese patients with advanced BTC, warranting phase 3 trials.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Sistema Biliar / Protocolos de Quimioterapia Combinada Antineoplásica / Anticuerpos Monoclonales Humanizados / Oxaliplatino Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Int J Cancer Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Sistema Biliar / Protocolos de Quimioterapia Combinada Antineoplásica / Anticuerpos Monoclonales Humanizados / Oxaliplatino Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Int J Cancer Año: 2021 Tipo del documento: Article País de afiliación: China