Zeng Z C, Tang Z Y, Liu K D, Lu J Z, Xie H, Yao Z
Liver Cancer Institute, Zhongshan Hospital, Shanghai Medical University, PR China.
J Cancer Res Clin Oncol. 1998;124(5):275-80. doi: 10.1007/s004320050166.
Resectional therapy has been accepted as the only curative therapy for hepatocellular carcinoma (HCC). Unfortunately, it is estimated that only 10% of HCC are resectable at the time of diagnosis. Cytoreduction and sequential resection offer a new hope for patients with unresectable HCC. Radioimmunotherapy (RIT) is an attractive approach for cytoreduction. We have previously shown that intrahepatic arterial 131I-labelled anti-HCC monoclonal antibody (131I-Hepama-1 mAb) could be used safely in combination with hepatic artery ligation for treatment of unresectable HCC, and encouraging results have been achieved. In this paper, the long-term survival and the prognostic factors in HCC patients treated with radioimmunotherapy will be analysed. Sixty-five patients with surgically verified unresectable HCC were treated with hepatic artery ligation plus hepatic artery cannulation and infusion from 1990 to 1992. Thirty-two patients were enrolled in a phase I-II clinical trial with infusion of 131I-radiolabelled anti-HCC monoclonal antibody (Hepama-1 mAb) via the hepatic artery (the RIT group). Another 33 patients formed the group treated with intrahepatic-arterial chemotherapy (the non-RIT group). T cell subsets were measured in 24 patients and human anti-(murine Ig) antibody (HAMA) were monitored in the RIT group. The 5-year survival rate was significantly higher in the RIT group than in the chemotherapy group, being 28.1% compared to 9.1% (P < 0.05); this was mainly a result of better cytoreduction and a higher sequential resection rate (53.1% compared to 9.1%). Significant prognostic factors in the RIT group included tumour capsule status and the number of tumour nodules. HAMA incidence and CD4+ T lymphocytes influenced short-term, but not long-term survival. It is suggested that intrahepatic-arterial RIT, using 131I-Hepama-1 mAb, combined with hepatic artery ligation might be an effective approach to improve long-term survival in some patients with unresectable HCC, which may successfully be made resectable by intra-arterial infusion of 131I-Hepama-1 mAb.
肝切除术已被公认为肝细胞癌(HCC)的唯一治愈性疗法。不幸的是,据估计,仅10%的HCC在诊断时可进行手术切除。肿瘤细胞减灭术及序贯切除术为无法进行手术切除的HCC患者带来了新希望。放射免疫疗法(RIT)是一种颇具吸引力的肿瘤细胞减灭方法。我们之前已表明,肝内动脉注射131I标记的抗HCC单克隆抗体(131I-Hepama-1 mAb)可安全地与肝动脉结扎术联合用于治疗无法进行手术切除的HCC,并已取得了令人鼓舞的结果。本文将分析接受放射免疫疗法治疗的HCC患者的长期生存率及预后因素。1990年至1992年期间,65例经手术证实无法进行手术切除的HCC患者接受了肝动脉结扎术加肝动脉插管及灌注治疗。32例患者参加了一项I-II期临床试验,通过肝动脉注入131I标记的抗HCC单克隆抗体(Hepama-1 mAb)(RIT组)。另外33例患者组成了接受肝内动脉化疗的治疗组(非RIT组)。对24例患者检测了T细胞亚群,并在RIT组监测了人抗(鼠Ig)抗体(HAMA)。RIT组的5年生存率显著高于化疗组,分别为28.1%和9.1%(P<0.05);这主要是更好的肿瘤细胞减灭及更高的序贯切除率(分别为53.1%和9.1%)的结果。RIT组的重要预后因素包括肿瘤包膜状态及肿瘤结节数量。HAMA发生率及CD4+T淋巴细胞影响短期生存率,但不影响长期生存率。提示采用131I-Hepama-1 mAb的肝内动脉RIT联合肝动脉结扎术可能是提高部分无法进行手术切除的HCC患者长期生存率的有效方法,通过肝动脉注入131I-Hepama-1 mAb可能成功使这些患者能够进行手术切除。