Mimaya J, Horikoshi Y, Shimizu H, Maeda H, Koizumi S, Kawakami K, Watanabe A, Utsumi J, Kikuta A, Oka T, Mugishima H, Kawamura N, Gushiken T, Ohta S, Yamamura Y, Ishida Y, Sekine I, Okada N, Fujimoto T
Division of Hemotology and Oncology, Shizuoka Children's Hospital.
Rinsho Ketsueki. 1997 Feb;38(2):100-7.
Treatment results were evaluated in 45 children with acute myeloblastic leukemia (AML) treated on the ANLL-9205 protocol of the Children's Cancer Leukemia Study Group (CCLSG, Japan). In this protocol, terarubicin (THP-ADR), vincristine and continuous infusion of cytosine arabinoside (Ara C) were applied for remission induction therapy (AVC), and VP16+ high dose Ara C were used sequentially for 32 or 48 weeks. Eleven patients received stem cell transplantation. Thirty-eight out of the 43 eligible patients (88.4%) achieved complete remission, and the overall 3-year event-free survival (EFS) was 55.6% (S.E.,10%). This favorable response was attributed mainly to the high induction rate of patients with the M5, M7 FAB subtypes and higher WBC counts (> or = 10 x 10(9)/L). There was no difference in the 3-year EFS of these patients who discontinued treatment between 32 weeks and 48 weeks. Serious toxicities were not observed in this study. These findings suggest that the ANLL-9205 protocol is an effective and safe treatment regimen for childhood AML. When comparing the treatment period of 32 or 48 weeks, the difference was not statistically significant.
对45例接受日本儿童癌症白血病研究组(CCLSG)ANLL - 9205方案治疗的急性髓细胞白血病(AML)患儿的治疗结果进行了评估。在该方案中,采用去甲柔红霉素(THP - ADR)、长春新碱及持续输注阿糖胞苷(Ara C)进行缓解诱导治疗(AVC),并依次使用VP16加用大剂量Ara C持续32周或48周。11例患者接受了干细胞移植。43例符合条件的患者中有38例(88.4%)实现完全缓解,3年无事件生存率(EFS)总体为55.6%(标准误,10%)。这种良好的反应主要归因于M5、M7 FAB亚型且白细胞计数较高(≥10×10⁹/L)的患者诱导缓解率高。在32周和48周停止治疗的这些患者的3年EFS方面没有差异。本研究未观察到严重毒性反应。这些发现表明,ANLL - 9205方案是儿童AML的一种有效且安全的治疗方案。比较32周或48周的治疗期时,差异无统计学意义。