Department of Medical Oncology Center, Bayi Affiliated Hospital, Nanjing University of Chinese Medicine, Nanjing, China.
Department of Interventional Radiology, Hunan Cancer Hospital, Changsha, China.
Int J Cancer. 2021 Dec 1;149(11):1944-1954. doi: 10.1002/ijc.33751. Epub 2021 Sep 8.
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.
胆管癌(BTC)是一种高度恶性肿瘤,治疗选择有限,预后较差。我们的研究旨在评估卡瑞利珠单抗联合奥沙利铂为基础的化疗作为晚期 BTC 的一线治疗。在中国进行的这项多中心、开放标签、2 期临床试验(ClinicalTrials.gov,NCT03092895)中,未经治疗的晚期 BTC 患者接受卡瑞利珠单抗(3mg/kg 静脉滴注,每 2 周一次)联合典型的 FOLFOX4(Cam-FOLFOX4 组;输注氟尿嘧啶、亚叶酸钙和奥沙利铂)或 GEMOX(Cam-GEMOX 组;输注吉西他滨和奥沙利铂)。主要终点是客观缓解率(ORR)。共纳入 92 例患者:29 例接受 Cam-FOLFOX4,63 例接受 Cam-GEMOX。确认的 ORR 和疾病控制率分别为 16.3%(95%CI=9.4-25.5)和 75.0%(95%CI=64.9-83.4)。中位缓解持续时间为 8.7 个月(95%CI=5.1-未达到)。中位无进展生存期和总生存期分别为 5.3 个月(95%CI=3.7-5.7)和 12.4 个月(95%CI=8.9-16.1)。接受 Cam-FOLFOX4 治疗的患者中有 82.8%和接受 Cam-GEMOX 治疗的患者中有 68.3%发生了≥3 级治疗相关不良事件(TRAEs),未观察到意外的影响。6 例(6.5%)患者因 TRAE 停止治疗。卡瑞利珠单抗联合 FOLFOX4 或 GEMOX 作为一线治疗对中国晚期 BTC 患者是有效且可耐受的,值得进行 3 期临床试验。