Kaneko M, Nishihira H, Mugishima H, Ohnuma N, Nakada K, Kawa K, Fukuzawa M, Suita S, Sera Y, Tsuchida Y
Department of Pediatric Surgery, University of Tsukuba, Japan.
Med Pediatr Oncol. 1998 Jul;31(1):1-7. doi: 10.1002/(sici)1096-911x(199807)31:1<1::aid-mpo1>3.0.co;2-h.
It has been shown that children aged more than 12 months with stage 3 and 4 neuroblastoma with N-myc amplification do worse than those without amplification. Development of an innovative chemotherapeutic protocol for patients in such an extremely poor-risk group was the purpose of this study.
Since March 1991 a new protocol for the treatment of advanced neuroblastoma was started. When N-myc was amplified more than 10-fold, patients received regimen A3, in which cyclophosphamide 1,200 mg/m2 was given on days 1 and 2; hence the dose of cytotoxic drugs was doubled. Patients with fewer than 10 copies of N-myc received regimen new A1, which is very similar to regimen A1 that had been used until March 1991 for all patients with advanced neuroblastoma with/without N-myc amplification. The efficacy of regimen A3 was evaluated.
The relapse-free survival rate at 1 and 2 years for stage 4 patients older than 12 months of age with N-myc amplification of more than 10-fold was 43% and 29%, respectively, with regimen A1 and that for the same subgroup of patients treated with regimen A3 since March 1991 was 79% and 49%, respectively; the difference is statistically significant. On the other hand, there were no differences in the relapse-free survival rate at 1 year and 2 years for stage 4 patients with fewer than 10 copies of N-myc between those treated with regimen A1 and those treated with new A1 since March 1991.
Stratification based on N-myc amplification into new A1 and A3 treatment protocols is of significant clinical importance. Regimen A3 was well tolerated and showed an improvement in clinical results in stage 4 patients with N-myc amplified more than 10-fold.
研究表明,12个月以上患有3期和4期神经母细胞瘤且N - myc基因扩增的儿童,其预后比未扩增的儿童更差。本研究的目的是为这一极高风险组的患者开发一种创新的化疗方案。
自1991年3月起,开始了一项治疗晚期神经母细胞瘤的新方案。当N - myc基因扩增超过10倍时,患者接受A3方案,即环磷酰胺1200mg/m²在第1天和第2天给药;因此细胞毒性药物的剂量加倍。N - myc基因拷贝数少于10个的患者接受新A1方案,该方案与1991年3月之前用于所有晚期神经母细胞瘤患者(无论有无N - myc基因扩增)的A1方案非常相似。评估了A3方案的疗效。
12个月以上、N - myc基因扩增超过10倍的4期患者,采用A1方案时1年和2年的无复发生存率分别为43%和29%,而自1991年3月起采用A3方案治疗的同一亚组患者的无复发生存率分别为79%和49%;差异具有统计学意义。另一方面,1991年3月以来,N - myc基因拷贝数少于10个的4期患者,采用A1方案治疗与采用新A1方案治疗的1年和2年无复发生存率没有差异。
基于N - myc基因扩增将患者分层为新A1和A3治疗方案具有重要的临床意义。A3方案耐受性良好,且在N - myc基因扩增超过10倍的4期患者中临床效果有所改善。