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多柔比星或柔红霉素在治疗窗内预先给药在新诊断的急性淋巴细胞白血病患儿中同样有效。在 CoALL 07-03 试验中的随机比较。

Doxorubicin or daunorubicin given upfront in a therapeutic window are equally effective in children with newly diagnosed acute lymphoblastic leukemia. A randomized comparison in trial CoALL 07-03.

机构信息

University Medical Center Hamburg-Eppendorf, Clinic of Pediatric Hematology and Oncology, Hamburg, Germany.

出版信息

Pediatr Blood Cancer. 2013 Feb;60(2):254-7. doi: 10.1002/pbc.24273. Epub 2012 Sep 4.

DOI:10.1002/pbc.24273
PMID:22948968
Abstract

BACKGROUND

The anthracyclines daunorubicin (DNR) and doxorubicin (DOX) are among the most important drugs in the treatment of childhood acute lymphoblastic leukemia, however there are conflicting in vitro data about the comparative efficacy and equivalent doses of both anthracyclines. To address the question of in vivo efficacy of both anthracyclines, patients enrolled in the CoALL 07-03 trial were randomized to receive one single dose of either doxorubicin 30 mg/m(2) , daunorubicin 30 mg/m(2) , or daunorubicin 40 mg/m(2) upfront induction therapy.

PROCEDURE

Children with newly diagnosed B-Precursor ALL or T-ALL were eligible for the randomized comparison. From the percentage of blasts and the white blood cell count (WBC) the absolute number of leukemic cells per µl peripheral blood (PB) was calculated and the initial value before DOX/DNR infusion equated as 100%. Main target criterion of this study was the leukemic cell decrease from Day 0 to Day 7.

RESULTS

Seven hundred forty three patients were randomized: 247 to the DOX; 252 to the DNR 30 mg/m(2) ; and DNR to the 40 mg/m(2) arm. The in vivo response was similar in all three treatment arms with a comparable blast decline in the peripheral blood. The percentages of patients with a clear non-response (M3 marrow) and moreover, the level of minimal residual disease (MRD) on Day 15 or at the end of induction were similar.

CONCLUSION

In vivo efficacy of a single dose daunorubicin 30 or 40 mg/m(2) is similar to that of doxorubicin given in a dose of 30 mg/m(2) .

摘要

背景

柔红霉素(DNR)和多柔比星(DOX)是治疗儿童急性淋巴细胞白血病的最重要药物之一,然而,关于这两种蒽环类药物的比较疗效和等效剂量,体外数据存在矛盾。为了解决这两种蒽环类药物的体内疗效问题,参与 CoALL 07-03 试验的患者被随机分配接受单剂量多柔比星 30mg/m²、柔红霉素 30mg/m²或柔红霉素 40mg/m²作为诱导治疗的一线药物。

过程

新诊断为 B-前体 ALL 或 T-ALL 的儿童有资格进行随机比较。根据blasts 的百分比和白细胞计数(WBC),外周血(PB)中每微升白血病细胞的绝对数量被计算出来,并且 DOX/DNR 输注前的初始值被等效为 100%。本研究的主要目标标准是从第 0 天到第 7 天白血病细胞的减少。

结果

743 名患者被随机分配:247 名患者接受 DOX;252 名患者接受 DNR 30mg/m²;DNR 组接受 40mg/m²。在所有三个治疗组中,体内反应相似,外周血中的 blast 下降程度相当。在所有三组治疗中,有明确无反应(骨髓 M3)的患者比例以及更重要的是,在第 15 天或诱导结束时的微小残留疾病(MRD)水平都相似。

结论

单剂量柔红霉素 30 或 40mg/m²的体内疗效与 30mg/m²剂量的多柔比星相似。

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