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A phase III, randomized, double-blind, controlled trial of carboxyamidotriazole plus chemotherapy for the treatment of advanced non-small cell lung cancer.

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机构: [1]Division of Pulmonary and Critical Care Medicine, Peking Union Medical College Hospital, Beijing, China. [2]Department of Medical Oncology, Chinese Academy of Medical Sciences Cancer Institute and Hospital, Beijing, China. [3]Department of Thoracic Oncology, Jilin Provincial Tumor Hospital, Changchun, China. [4]Division of Oncology, Linyi Cancer Hospital, Linyi, China. [5]Division of Pulmonary Medicine, The First Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China. [6]Division of Oncology, Tangdu Hospital, Xi'an, China. [7]Thoracic Surgery, Yunnan Cancer Hospital, Kunming, China. [8]Division of Oncology, Hebei Medical University Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, China. [9]Division of Oncology, Cancer Hospital of Shantou University Medical College, Shantou, China. [10]Division of Thoracic Oncology, Sichuan University West China Hospital, Chengdu, China. [11]Division of Oncology, Capital Medical University Beijing Chest Hospital, Beijing, China. [12]Cancer Center, Jilin University First Hospital, Changchun, China.
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Carboxyamidotriazole (CAI), a calcium channel blocker, inhibits tumor cell proliferation, metastasis, and angiogenesis. This trial aimed to determine whether CAI combined with conventional chemotherapy could prolong progression-free survival (PFS) in non-small cell lung cancer (NSCLC) patients. Patients were assigned into groups (3:1 ratio) to receive either chemotherapy + CAI or chemotherapy alone. Cisplatin (25 mg/m2) was administered by intravenous infusion on days 1, 2, and 3, and vinorelbine (25 mg/m2) on days 1 and 8 of each 3-week cycle for four cycles. CAI was administered at 100 mg daily with concomitant chemotherapy; this treatment was continued after chemotherapy was ceased until serious toxicity or disease progression had occurred. PFS was the primary endpoint, and the secondary endpoints were objective response rate (ORR), disease control rate, overall survival (OS), and quality of life. In total, 495 patients were enrolled in the trial: 378 in the chemotherapy + CAI group and 117 in the chemotherapy + placebo group. PFS was significantly greater in the chemotherapy + CAI [median, 134 days; 95% confidence interval (CI) 127-139] than in the chemotherapy + placebo (median, 98 days; 95% CI: 88-125) group, with a hazard ratio of 0.690 (95% CI: 0.539-0.883; p = 0.003). There was no difference in the OS rates of both groups. The ORR was greater in the chemotherapy + CAI group than in the chemotherapy + placebo group (34.6% versus 25.0%, p = 0.042). Adverse events of ⩾grade 3 occurred more frequently in the CAI group [256 (68.1%) versus 64 (55.2%); p = 0.014]. CAI + platinum-based chemotherapy prolonged PFS and could be a useful therapeutic option to treat NSCLC. chinadrugtrials.org.cn identifier: CTR20160395. © The Author(s), 2020.

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大类 | 2 区 医学
小类 | 2 区 肿瘤学
最新[2023]版:
大类 | 2 区 医学
小类 | 3 区 肿瘤学
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Q1 ONCOLOGY
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Q2 ONCOLOGY

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第一作者机构: [1]Division of Pulmonary and Critical Care Medicine, Peking Union Medical College Hospital, Beijing, China.
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通讯机构: [*1]Department of Medical Oncology, Chinese Academy of Medical Sciences Cancer Hospital, 17 Panjiayuan Nanli, Chaoyang District, Beijing, 100021, China. [*2]Division of Pulmonary and Critical Care Medicine, Peking Union Medical College Hospital, No. 1 Shuaifuyuan Wangfujing, Dongcheng District, Beijing, 100730, China.
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