Hiyama Eiso, Ueda Yuka, Onitake Yoshiyuki, Kurihara Shou, Watanabe Kenichiro, Hishiki Tomoro, Tajiri Tatsuro, Ida Komei, Yano Michihiro, Kondo Satoshi, Oue Takaharu
Department of Pediatric Surgery, Hiroshima University Hospital, Hiroshima, Japan,
Pediatr Surg Int. 2013 Oct;29(10):1071-5. doi: 10.1007/s00383-013-3399-0.
The Japanese Study Group for Pediatric Liver Tumor (JPLT) has conducted cooperative treatment studies on hepatoblastoma (HBL) since 1991. The JPLT2 protocol was launched in 1999 to evaluate the efficacy of cisplatin/pirarubicin (CITA) under risk stratification. European and North American groups showed the improvement of HBL patients by pre- and postoperative chemotherapeutic regimens. Therefore, we evaluated the results of JPLT study and considered the future aspect of JPLT.
A total of 389 children with malignant hepatic tumors were enrolled in JPLT-2 until 2010. Data from 331 HBL cases were analyzed.
Of the 331 patients enrolled, their 5-year overall survival and event-free survival rates were 83.3 and 68.0%, respectively. While outcomes of standard-risk cases (tumors involving 3 or fewer sectors of the liver) were excellent, those of high-risk cases (tumors involving 4 sectors of the liver or with distant metastases) remained poor. For 26 high-risk or relapse/refractory HBL cases, high-dose chemotherapy (HDC) with stem cell transplantation (SCT) was carried out. Among them, 6 of 12 relapse or refractory cases died. Compared with other regimens, the CITA regimen achieved similar or superior rates of survival among children with standard-risk HBL, while HDC with SCT was not effective in patients with high-risk HBL. Presently, a global Children's Hepatic Tumor International Consortium (CHIC) project is ongoing, with a focus on international cooperation and risk stratification in the field of rare liver cancers in children. More promising strategies, including liver transplantation and new targeting drugs under global risk stratification, are being proposed.
自1991年以来,日本小儿肝脏肿瘤研究组(JPLT)一直在开展肝母细胞瘤(HBL)的联合治疗研究。1999年启动了JPLT2方案,以评估顺铂/吡柔比星(CITA)在风险分层下的疗效。欧洲和北美研究组显示,术前和术后化疗方案改善了HBL患者的病情。因此,我们评估了JPLT研究的结果,并考虑了JPLT的未来发展方向。
截至2010年,共有389例儿童恶性肝肿瘤患者纳入JPLT-2研究。对331例HBL病例的数据进行了分析。
在纳入的331例患者中,其5年总生存率和无事件生存率分别为83.3%和68.0%。虽然标准风险病例(肿瘤累及肝脏3个或更少肝段)的预后良好,但高风险病例(肿瘤累及4个肝段或有远处转移)的预后仍然较差。对26例高风险或复发/难治性HBL病例进行了高剂量化疗(HDC)联合干细胞移植(SCT)。其中,12例复发或难治性病例中有6例死亡。与其他方案相比,CITA方案在标准风险HBL儿童中的生存率相似或更高,而HDC联合SCT对高风险HBL患者无效。目前,一项全球儿童肝脏肿瘤国际联盟(CHIC)项目正在进行中,重点是儿童罕见肝癌领域的国际合作和风险分层。正在提出更有前景的策略,包括全球风险分层下的肝移植和新型靶向药物。