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.
Lancet Gastroenterol Hepatol. 2020 Jun;5(6):548-560. doi: 10.1016/S2468-1253(19)30422-4. Epub 2020 Mar 9.
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.
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.
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.
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.
State Key Project on Infectious Diseases of China.
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。
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。
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。
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。
中国传染病重大专项。