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索拉非尼联合肝动脉灌注化疗与索拉非尼治疗伴有主要门静脉肿瘤血栓形成的肝细胞癌的随机试验

Sorafenib Plus Hepatic Arterial Infusion Chemotherapy versus Sorafenib for Hepatocellular Carcinoma with Major Portal Vein Tumor Thrombosis: A Randomized Trial.

作者信息

Zheng Kanglian, Zhu Xu, Fu Shijie, Cao Guang, Li Wen-Qing, Xu Liang, Chen Hui, Wu Di, Yang Renjie, Wang Kun, Liu Wei, Wang Hongwei, Bao Quan, Liu Ming, Hao Chunyi, Shen Lin, Xing Baocai, Wang Xiaodong

机构信息

From the Departments of Interventional Oncology (K.Z., X.Z., S.F., G.C., L.X., H.C., D.W., R.Y., X.W.), Cancer Epidemiology (W.Q.L.), Hepatic and Biliary Surgery (K.W., W.L., H.W., Q.B., M.L., C.H., B.X.), and Gastrointestinal Oncology (L.S.), Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Peking University Cancer Hospital and Institute, Beijing 100142, China.

出版信息

Radiology. 2022 May;303(2):455-464. doi: 10.1148/radiol.211545. Epub 2022 Feb 1.

Abstract

Background The prognosis of hepatocellular carcinoma (HCC) with major portal vein tumor thrombosis (PVTT) is dismal after standard treatment with sorafenib. Hepatic arterial infusion chemotherapy (HAIC) has been suggested for patients with HCC and major PVTT. Purpose To compare the efficacy and safety of sorafenib plus 3cir-OFF HAIC versus sorafenib alone for advanced HCC with major PVTT. Materials and Methods This phase II trial recruited systemic treatment-naïve patients with HCC and major PVTT (portal vein invasion grade Vp3 [first branch] and Vp4 [main trunk]) between June 2017 and November 2019. Patients were randomly assigned (1:1 ratio) to receive sorafenib (400 mg twice daily) plus 3cir-OFF HAIC (35 mg/m oxaliplatin [hours 0-2] followed by 600 mg/m 5-fluorouracil [hours 2-24], days 1-3) with a standardized percutaneous port catheter system or sorafenib alone (400 mg twice daily) every 4 weeks. The primary end point was overall survival (OS). The secondary end points were objective response rate, progression-free survival (PFS), and safety. OS and PFS were assessed using the Kaplan-Meier method and log-rank test. Results The intent-to-treat population included 64 patients, with 32 in each group. The median OS was 16.3 months (95% CI: 0.0, 35.5) with sorafenib plus HAIC and 6.5 months (95% CI: 4.4, 8.6) with sorafenib alone (hazard ratio [HR] = 0.28; 95% CI: 0.15, 0.53; < .001). A higher objective response rate (41% [ = 13] vs 3% [ = 1], < .001) and a longer median PFS (9.0 months vs 2.5 months; HR = 0.26; 95% CI: 0.15, 0.47; < .001) were observed in the sorafenib plus HAIC group. Grade 3 or 4 adverse events were more frequent in the sorafenib plus HAIC group, including diarrhea ( = 7 [22%] vs = 5 [16%]), hand-foot syndrome ( = 6 [19%] vs = 2 [6%]), and thrombocytopenia ( = 7 [22%] vs = 0). Conclusion Sorafenib plus 3cir-OFF hepatic arterial infusion chemotherapy may be a promising treatment in patients with hepatocellular carcinoma and major portal vein tumor thrombosis because of the improved survival and an acceptable safety profile. Clinical trial registration no. NCT03009461 © RSNA, 2022 See also the editorial by Chung in this issue.

摘要

背景

在接受索拉非尼标准治疗后,伴有主要门静脉肿瘤血栓形成(PVTT)的肝细胞癌(HCC)预后不佳。对于HCC合并主要PVTT的患者,已有人提出肝动脉灌注化疗(HAIC)。目的:比较索拉非尼联合3cir - OFF HAIC与单独使用索拉非尼治疗伴有主要PVTT的晚期HCC的疗效和安全性。材料与方法:本II期试验纳入了2017年6月至2019年11月期间未接受过全身治疗的HCC合并主要PVTT(门静脉侵犯分级为Vp3[第一分支]和Vp4[主干])患者。患者按1:1比例随机分配,接受索拉非尼(400mg,每日2次)联合3cir - OFF HAIC(35mg/m²奥沙利铂[0 - 2小时],随后600mg/m²氟尿嘧啶[2 - 24小时],第1 - 3天),采用标准化经皮端口导管系统,或每4周单独使用索拉非尼(400mg,每日2次)。主要终点为总生存期(OS)。次要终点为客观缓解率、无进展生存期(PFS)和安全性。采用Kaplan - Meier法和对数秩检验评估OS和PFS。结果:意向性治疗人群包括64例患者,每组32例。索拉非尼联合HAIC组的中位OS为16.3个月(95%CI:0.0,35.5),单独使用索拉非尼组为6.5个月(95%CI:4.4,8.6)(风险比[HR]=0.28;95%CI:0.15,0.53;P<0.001)。索拉非尼联合HAIC组观察到更高的客观缓解率(41%[n = 13]对3%[n = 1],P<0.001)和更长的中位PFS(9.0个月对2.5个月;HR = 0.26;95%CI:0.15,0.47;P<0.001)。索拉非尼联合HAIC组3级或4级不良事件更常见,包括腹泻(n = 7[22%]对n = 5[16%])、手足综合征(n = 6[19%]对n = 2[6%])和血小板减少症(n = 7[22%]对n = 0)。结论:索拉非尼联合3cir - OFF肝动脉灌注化疗可能是治疗肝细胞癌合并主要门静脉肿瘤血栓形成患者的一种有前景的治疗方法,因为其提高了生存率且安全性可接受。临床试验注册号:NCT03009461 © RSNA,2022 另见本期Chung的社论。

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