中国不可切除肝细胞癌患者接受 Nivolumab 治疗的真实世界经验。

IF 1.4 Q4 GASTROENTEROLOGY & HEPATOLOGY Gastroenterology Research Pub Date : 2024-02-01 Epub Date: 2024-02-28 DOI:10.14740/gr1684
Shou-Wu Lee, Sheng-Shun Yang, Teng-Yu Lee
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引用次数: 0

摘要

背景:对于无法切除的肝细胞癌(HCC),nivolumab(抗程序性死亡受体-1(PD-1))被用作非根治性干预药物。本研究的目的是关注nivolumab在HCC患者中应用的实际经验:招募2018年6月至2020年5月期间在台中荣民总医院接受nivolumab治疗的无法切除的HCC患者。排除标准为Child-Pugh C期、表现状态不佳、缺乏依从性或不能耐受药物治疗。收集并分析入组患者的肿瘤放射学反应和生存结果:结果:在57名患者中,大部分患者属于Child-Pugh A期(70.2%)和巴塞罗那临床肝癌(BCLC)C期(66.7%)。14名患者(24.6%)接受了Nivolumab作为一线治疗,43名患者(75.4%)接受了二线系统治疗。平均疗程为6.5个月。客观反应率(ORR)为24.6%,疾病控制率(DCR)为42.1%。中位无进展生存期(PFS)为5.8个月(95% 置信区间(CI):1.1 - 10.6),总生存期(OS)为11.5个月(95% CI:4.3 - 17.8)。免疫相关不良事件(IRAE)为8.8%。治疗期间出现甲胎蛋白(AFP)反应(AFP从基线下降≥10%)可预测肿瘤放射学反应(客观反应:危险比(HR):4.89,95% CI:1.14 - 21.00;疾病控制:HR:4.71,95% CI:1.32 - 16.81)。肿瘤放射学反应患者的PFS和OS时间更长:结论:治疗期间甲胎蛋白的下降可预测HCC对nivolumab的放射学反应。结论:治疗期间甲胎蛋白的下降对HCC对尼伐单抗的放射学反应有预测作用,获得放射学反应的患者生存期更长。
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A Real-World Experience on a Chinese Population of Patients With Unresectable Hepatocellular Carcinoma Treated With Nivolumab.

Background: For unresectable hepatocellular carcinoma (HCC), nivolumab (anti-programmed death receptor-1 (PD-1)) is used as non-curative interventions. The aim of the study was to focus on the real-world experience of nivolumab applied to patients with HCC.

Methods: Unresectable HCC patients receiving nivolumab treatments at Taichung Veterans General Hospital, from June 2018 to May 2020, were recruited. Exclusion criteria were Child-Pugh stage C, poor performance status, a lack of compliance or intolerable to drug treatments. The tumor radiological responses and survival outcomes of enrolled patients were collected and analyzed.

Results: Among a total of 57 patients, most of them were classified as Child-Pugh stage A (70.2%) and Barcelona Clinic Liver Cancer (BCLC) stage C (66.7%). Nivolumab was given to 14 (24.6%) as the primary-line, and 43 patients (75.4%) as the secondary-line systemic treatments. The mean therapeutic duration was 6.5 months. Objective response rate (ORR) was 24.6%, and disease control rate (DCR) was 42.1%. The overall median progression-free survival (PFS) was 5.8 months (95% confidence interval (CI): 1.1 - 10.6), and overall survival (OS) was 11.5 months (95% CI: 4.3 - 17.8). Immune-related adverse event (IRAE) was 8.8%. Presence of alpha-fetoprotein (AFP) response (a decline in AFP ≥ 10% from baseline) during therapy predicted the tumor radiological response (to objective response: hazard ratio (HR): 4.89, 95% CI: 1.14 - 21.00; to disease control: HR: 4.71, 95% CI: 1.32 - 16.81). Those with tumor radiological responses showed longer PFS and OS.

Conclusions: Decline in AFP during therapy has a predicting role on HCC radiological responses to nivolumab. Achieving radiological responses had better survival outcomes.

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Gastroenterology Research
Gastroenterology Research GASTROENTEROLOGY & HEPATOLOGY-
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