Tawada Akinobu, Chiba Tetsuhiro, Ooka Yoshihiko, Kanogawa Naoya, Saito Tomoko, Motoyama Tenyu, Ogasawara Sadahisa, Suzuki Eiichiro, Kanai Fumihiko, Yoshikawa Masaharu, Yokosuka Osamu
Department of Gastroenterology and Nephrology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Department of Gastroenterology and Nephrology, Graduate School of Medicine, Chiba University, Chiba, Japan
Anticancer Res. 2015 Jan;35(1):549-54.
We aimed to evaluate the therapeutic efficacy of transcatheter arterial chemoembolization (TACE) using miriplatin plus epirubicin in unresectable hepatocellular carcinoma (HCC).
The efficacy of TACE was evaluated by dynamic computed tomography (CT) or magnetic resonance imaging (MRI) three months after the procedure according to the Response Evaluation Criteria in Cancer Study Group of Japan. Adverse events (AEs), including clinical symptoms, hematological toxicities and blood chemistry toxicities, were assessed using Common Terminology Criteria Version 4.0.
Thirty patients with HCC received TACE with miriplatin (miriplatin group) and 29 patients received TACE with miriplatin plus epirubicin (miriplatin-plus-epirubicin group). AEs, such as anorexia and neutropenia, were observed more frequently in the miriplatin-plus-epirubicin group than in the miriplatin group (p=0.028 and 0.014, respectively). However, there was no significant difference in the incidence of these AEs (grade 3/4) between groups. The objective response rate (ORR), including the complete response (CR) and partial response (PR), was 76.7% in the miriplatin group and 58.6% in the miriplatin-plus-epirubicin group (p=0.224). The median time to progression (TTP) in the miriplatin group and the miriplatin-plus-epirubicin group was 8.2 and 6.1 months, respectively (p=0.123).
Although TACE with miriplatin plus epirubicin was safe and tolerable, no additional anti-tumor effects were observed compared to TACE with miriplatin. Further analysis is required to refine the efficacy of TACE using miriplatin plus epirubicin.
我们旨在评估米铂联合表柔比星经动脉化疗栓塞术(TACE)治疗不可切除肝细胞癌(HCC)的疗效。
根据日本癌症研究组的疗效评价标准,在术后三个月通过动态计算机断层扫描(CT)或磁共振成像(MRI)评估TACE的疗效。使用《通用术语标准》第4.0版评估不良事件(AE),包括临床症状、血液学毒性和血液化学毒性。
30例HCC患者接受了米铂TACE治疗(米铂组),29例患者接受了米铂联合表柔比星TACE治疗(米铂联合表柔比星组)。米铂联合表柔比星组出现厌食和中性粒细胞减少等不良事件的频率高于米铂组(分别为p = 0.028和0.014)。然而,两组间这些不良事件(3/4级)的发生率无显著差异。包括完全缓解(CR)和部分缓解(PR)在内的客观缓解率(ORR)在米铂组为76.7%,在米铂联合表柔比星组为58.6%(p = 0.224)。米铂组和米铂联合表柔比星组的中位疾病进展时间(TTP)分别为8.2个月和6.1个月(p = 0.123)。
尽管米铂联合表柔比星TACE安全且可耐受,但与米铂TACE相比,未观察到额外的抗肿瘤效果。需要进一步分析以明确米铂联合表柔比星TACE的疗效。