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辅助 I-美妥昔单抗治疗肝癌切除术后:一项随机、对照、多中心、开放标签、2 期临床试验。

Adjuvant I-metuximab for hepatocellular carcinoma after liver resection: a randomised, controlled, multicentre, open-label, phase 2 trial.

机构信息

Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.

Cell Engineering Research Center, Fourth Military Medical University, Xi'an, China.

出版信息

Lancet Gastroenterol Hepatol. 2020 Jun;5(6):548-560. doi: 10.1016/S2468-1253(19)30422-4. Epub 2020 Mar 9.

Abstract

BACKGROUND

Effective adjuvant treatment after hepatectomy for hepatocellular carcinoma (HCC) is an important area of research. Radioactive iodine (I)-labelled metuximab is a radiolabelled monoclonal antibody against the CD147 (also known as basigin or HAb18G) antigen that is expressed in HCC. We aimed to examine the role of I-metuximab as an adjuvant therapy after HCC resection.

METHODS

This randomised, controlled, multicentre, open-label, phase 2 trial was done at five medical centres in China. Patients aged 18-75 years who underwent curative-intent resection of histologically confirmed HCC expressing CD147 were randomly assigned (1:1) by a computer-generated random sequence, stratified by centre, to receive either adjuvant transarterial injection of one dose of 27·75 MBq/kg I-metuximab 4-6 weeks after the hepatectomy (treatment group) or no adjuvant treatment (control group). Patients and physicians were not masked to the study groups. The primary outcome was 5-year recurrence-free survival (RFS) in the intention-to-treat population. This trial is registered with ClinicalTrials.gov, NCT00819650.

FINDINGS

Between April 1, 2009, and Nov 30, 2012, 485 patients were screened for eligibility. 329 (68%) of these patients were excluded and 156 (32%) were randomly assigned to receive either I-metuximab (n=78) or no adjuvant treatment (n=78). The median follow-up was 55·9 months (IQR 18·6-79·4). In the intention-to-treat population, the 5-year RFS was 43·4% (95% CI 33·6-55·9) in the I-metuximab group and 21·7% (14·2-33·1) in the control group (hazard ratio 0·49 [95% CI 0·34-0·72]; Z=2·96, p=0·0031). I-metuximab-associated adverse events occurred within the first 4 weeks in 34 (45%) of 76 patients, seven (21%) of whom had grade 3 or 4 adverse events. These adverse events were all resolved with appropriate treatment within 2 weeks of being identified.

INTERPRETATION

Adjuvant I-metuximab treatment significantly improved the 5-year RFS of patients after hepatectomy for HCC tumours expressing CD147. This treatment was well tolerated by patients.

FUNDING

State Key Project on Infectious Diseases of China.

摘要

背景

肝癌(HCC)手术后有效的辅助治疗是一个重要的研究领域。放射性碘(I)标记的美妥昔单抗是一种针对 CD147(也称为 basigin 或 HAb18G)抗原的放射性标记单克隆抗体,该抗原在 HCC 中表达。我们旨在研究 I-美妥昔单抗作为 HCC 切除术后辅助治疗的作用。

方法

这是一项在中国五家医疗中心进行的随机、对照、多中心、开放标签、二期临床试验。纳入年龄在 18-75 岁之间、接受组织学证实的 CD147 表达 HCC 根治性切除术的患者,按 1:1 比例由计算机生成的随机序列分层(按中心),随机分为辅助经肝动脉注射一次 27.75MBq/kg 的 I-美妥昔单抗组(治疗组)或不接受辅助治疗组(对照组)。患者和医生对研究组均不知情。主要终点为意向治疗人群的 5 年无复发生存率(RFS)。该试验在 ClinicalTrials.gov 注册,NCT00819650。

结果

2009 年 4 月 1 日至 2012 年 11 月 30 日期间,共筛选了 485 例患者,其中 329 例(68%)被排除,156 例(32%)被随机分配接受 I-美妥昔单抗(n=78)或不接受辅助治疗(n=78)。中位随访时间为 55.9 个月(IQR 18.6-79.4)。在意向治疗人群中,I-美妥昔单抗组的 5 年 RFS 为 43.4%(95%CI 33.6-55.9),对照组为 21.7%(14.2-33.1)(风险比 0.49[95%CI 0.34-0.72];Z=2.96,p=0.0031)。在 76 例接受治疗的患者中,有 34 例(45%)在治疗后的 4 周内发生了与 I-美妥昔单抗相关的不良事件,其中 7 例(21%)发生了 3 级或 4 级不良事件。这些不良事件在发现后的 2 周内都通过适当的治疗得到了缓解。

结论

辅助 I-美妥昔单抗治疗可显著改善 HCC 术后 CD147 表达肿瘤患者的 5 年 RFS。这种治疗方法患者耐受性良好。

资金来源

中国传染病重大专项。

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