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基于N-myc扩增状态对4期神经母细胞瘤患者进行分层治疗。日本晚期神经母细胞瘤治疗研究组,东京,日本。

Stratification of treatment of stage 4 neuroblastoma patients based on N-myc amplification status. Study Group of Japan for Treatment of Advanced Neuroblastoma, Tokyo, Japan.

作者信息

Kaneko M, Nishihira H, Mugishima H, Ohnuma N, Nakada K, Kawa K, Fukuzawa M, Suita S, Sera Y, Tsuchida Y

机构信息

Department of Pediatric Surgery, University of Tsukuba, Japan.

出版信息

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.

Abstract

BACKGROUND

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.

PROCEDURE

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

程序

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。

结果

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。

结论

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。

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