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儿童高危急性淋巴细胞白血病缓解后:AIEOP ALL 2000 研究中化疗或移植的结果。

Childhood high-risk acute lymphoblastic leukemia in first remission: results after chemotherapy or transplant from the AIEOP ALL 2000 study.

机构信息

Department of Pediatrics, Ospedale S. Gerardo, University of Milano-Bicocca, Fondazione MBBM, Monza, Italy;

出版信息

Blood. 2014 Mar 6;123(10):1470-8. doi: 10.1182/blood-2013-10-532598. Epub 2014 Jan 10.

Abstract

The outcome of high-risk (HR) acute lymphoblastic leukemia patients enrolled in the AIEOP-BFM ALL 2000 study in Italy is described. HR criteria were minimal residual disease (MRD) levels ≥10(-3) at day 78 (MRD-HR), no complete remission (CR) at day 33, t(4;11) translocation, and prednisone poor response (PPR). Treatment (2 years) included protocol I, 3 polychemotherapy blocks, delayed intensification (protocol IIx2 or IIIx3), cranial radiotherapy, and maintenance. A total of 312 HR patients had a 5-year event-free survival (EFS) of 58.9% (standard error [SE] = 2.8) and an overall survival of 68.9% (SE = 2.6). In hierarchical order, EFS was 45.9% (4.4) in 132 MRD-HR patients, 41.2% (11.9) in 17 patients with no CR at day 33, 36.4% (14.5) in 11 patients with t(4;11), and 74.0% (3.6) in 152 HR patients only for PPR. No statistically significant difference was found for disease-free survival in patients with very HR features [MRD-HR, no CR at day 33, t(4;11) translocation], given hematopoietic stem cell transplantation (HSCT) (n = 66) or chemotherapy only (n = 88), after adjusting for waiting time to HSCT (5.7 months). Patients at HR only for PPR have a favorable outcome. MRD-HR is associated with poor outcome despite intensive treatment and/or HSCT and may qualify for innovative therapies. The study was registered at www.clinicaltrials.gov as #NCT00613457.

摘要

意大利 AIEOP-BFM ALL 2000 研究入组的高危 (HR) 急性淋巴细胞白血病患者的结局。HR 标准为第 78 天(MRD-HR)时微小残留病 (MRD) 水平≥10(-3)、第 33 天未达完全缓解 (CR)、t(4;11)易位和泼尼松不良反应 (PPR)。治疗(2 年)包括方案 I、3 个化疗方案、延迟强化(方案 IIx2 或 IIIx3)、颅放疗和维持治疗。共 312 例 HR 患者的 5 年无事件生存率(EFS)为 58.9%(标准误差 [SE] = 2.8),总生存率为 68.9%(SE = 2.6)。按层次顺序,132 例 MRD-HR 患者的 EFS 为 45.9%(4.4),33 天无 CR 的 17 例患者的 EFS 为 41.2%(11.9),11 例 t(4;11)患者的 EFS 为 36.4%(14.5),仅 PPR 的 152 例 HR 患者的 EFS 为 74.0%(3.6)。在调整等待 HSCT 的时间(5.7 个月)后,对于接受造血干细胞移植 (HSCT)(n = 66)或仅化疗(n = 88)的 HR 患者,无疾病生存差异无统计学意义。仅 PPR 的患者有较好的结局。尽管采用了强化治疗和/或 HSCT,MRD-HR 仍与不良预后相关,可能适合创新疗法。该研究在 www.clinicaltrials.gov 上注册为 #NCT00613457。

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