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尝试优化无核心结合因子的儿童急性髓细胞白血病的诱导后治疗:来自日本儿科白血病/淋巴瘤研究组(JPLSG)的报告。

Attempts to optimize postinduction treatment in childhood acute myeloid leukemia without core-binding factors: A report from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG).

机构信息

Department of Hematology and Oncology, Kobe Children's Hospital, Hyogo, Japan.

Higashiosaka Aramoto Heiwa Clinic, Osaka, Japan.

出版信息

Pediatr Blood Cancer. 2020 Dec;67(12):e28692. doi: 10.1002/pbc.28692. Epub 2020 Sep 4.

Abstract

We previously reported that risk-stratified therapy and intensive postremission chemotherapy (PRC) contributed to the improved survival of childhood acute myeloid leukemia (AML) in the AML99 study, which led us to consider a reduction in the number of PRC courses with more restrictive indications for stem cell transplantation (SCT) in the successor AML-05 study. We here report the outcome of AML patients without core-binding factor mutation (non-CBF AML) in the AML-05 study. Two-hundred eighty-nine children (age < 18 years old) with non-CBF AML were eligible. Patients with unfavorable cytogenetics and/or poor bone marrow response to the first induction course were candidates for SCT in the AML-05 study. After two courses of induction, a further three courses of PRC were given in AML-05, while four courses were given in the AML99 study. The 3-year event-free survival (EFS) rate in the AML-05 study (46.7%, 95% CI: 40.6-52.6%) was comparable to that of non-CBF AML in the AML99 study (51.5%, 95% CI: 42.7-59.6%) (P = .16). However, the 3-year overall survival (OS) rate in the AML-05 study (62.9%, 95% CI: 56.3-68.8%) was slightly lower than that in the AML99 study (71.6%, 95% CI: 63.2-78.5%) (P = .060), mainly due to decreased remission induction rate and increased nonrelapsed mortality. In conclusion, reductions in the number of PRC courses from four to three, together with repetitive cycles of high-dose cytarabine, were acceptable for non-CBF childhood AML.

摘要

我们之前报道过,风险分层治疗和强化缓解后化疗(PRC)有助于改善 AML99 研究中儿童急性髓系白血病(AML)的生存结果,这促使我们考虑在后继 AML-05 研究中减少 PRC 疗程数量,并对干细胞移植(SCT)的适应证进行更严格的限制。我们在此报告 AML-05 研究中非核心结合因子突变(非 CBF AML)患者的结果。共有 289 名年龄<18 岁的非 CBF AML 患儿符合条件。AML-05 研究中,具有不良细胞遗传学和/或初次诱导疗程后骨髓反应不良的患者为 SCT 候选者。在 AML-05 中,在进行两个疗程的诱导后,再进行三个疗程的 PRC,而在 AML99 中进行四个疗程的 PRC。AML-05 研究中 3 年无事件生存(EFS)率(46.7%,95%CI:40.6-52.6%)与 AML99 研究中非 CBF AML(51.5%,95%CI:42.7-59.6%)相当(P=0.16)。然而,AML-05 研究中 3 年总生存(OS)率(62.9%,95%CI:56.3-68.8%)略低于 AML99 研究(71.6%,95%CI:63.2-78.5%)(P=0.060),主要原因是缓解诱导率降低和非复发死亡率增加。总之,将 PRC 疗程从四个减少到三个,同时进行重复的高剂量阿糖胞苷周期,对非 CBF 儿童 AML 是可以接受的。

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