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基于微小残留病灶的一线达沙替尼联合化疗治疗成人费城染色体阳性急性淋巴细胞白血病的疗效和长期预后。

Minimal residual disease-based effect and long-term outcome of first-line dasatinib combined with chemotherapy for adult Philadelphia chromosome-positive acute lymphoblastic leukemia.

机构信息

Department of Hematology, Catholic BMT Center; Leukemia Research Institute, College of Medicine, The Catholic University of Korea, Seoul.

Division of Hematology-Oncology, Department of Internal Medicine, Chonbuk National University Medical School, Jeonju.

出版信息

Ann Oncol. 2016 Jun;27(6):1081-1088. doi: 10.1093/annonc/mdw123. Epub 2016 Mar 6.

Abstract

BACKGROUND

The use of imatinib combined with chemotherapy has demonstrated improved outcome in adults with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph-positive ALL). However, a substantial proportion of patients continue to die as a result of disease progression.

PATIENTS AND METHODS

We assessed the minimal residual disease (MRD)-based effect and long-term outcome of first-line incorporation of dasatinib (100 mg once daily) into chemotherapy alternatively for adults with Ph-positive ALL. The primary end point was the major molecular response (MMR) rate by the end of the second dasatinib cycle. Patients with a donor proceeded to allogeneic stem cell transplantation (SCT) as early as possible. MRD monitoring was centrally evaluated by real-time quantitative polymerase chain reaction (4.5-log sensitivity) using bone marrow samples.

RESULTS

Fifty-one patients (median age, 46 years) were enrolled and treated with this strategy. After the first dasatinib cycle, 50 patients (98.0%) achieved complete remission (CR). By the end of the second dasatinib cycle, 46 (93.9%) of 49 assessable patients had persistent CR, and 38 (77.6%) had MMR (32.7%) or undetectable MRD (44.9%). On the basis of the MRD kinetics by this time point, the numbers of early-stable, late, and poor molecular responders were 23 (46.9%), 15 (30.7%), and 11 (22.4%), respectively. Thirty-nine patients (76.5%) underwent allogeneic SCT in CR1. After a median follow-up of 54 months, the 4-year cumulative incidence of relapse and disease-free survival (DFS) rate for all patients were 30.0% and 52.0%, respectively, and the corresponding outcomes among those receiving allogeneic SCT in CR1 were 20.5% and 64.1%, respectively. Poor molecular responders had a higher risk of relapse and DFS than those of early-stable molecular responders.

CONCLUSION

This dasatinib-based protocol was effective for achieving a good quality molecular response and durable DFS in adults with Ph-positive ALL.

TRIAL REGISTRATION

clinicaltrials.gov, NCT01004497.

摘要

背景

伊马替尼联合化疗已证明可改善费城染色体阳性急性淋巴细胞白血病(Ph 阳性 ALL)成人患者的预后。然而,仍有相当一部分患者因疾病进展而死亡。

患者和方法

我们评估了 dasatinib(每天 100mg,1 次)替代化疗一线治疗 Ph 阳性 ALL 成人患者的基于微小残留病(MRD)的疗效和长期结果。主要终点是第 2 个 dasatinib 周期末的主要分子缓解(MMR)率。有供者的患者尽早进行异基因造血干细胞移植(SCT)。通过实时定量聚合酶链反应(4.5 个对数的灵敏度)对骨髓样本进行中心评估来监测 MRD。

结果

51 例患者(中位年龄,46 岁)入组并接受了这种治疗策略。在第 1 个 dasatinib 周期后,50 例(98.0%)患者达到完全缓解(CR)。在第 2 个 dasatinib 周期末,49 例可评估患者中 46 例(93.9%)持续 CR,38 例(77.6%)达到 MMR(32.7%)或无法检测到 MRD(44.9%)。基于此时点的 MRD 动力学,早期稳定、晚期和不良分子反应者的数量分别为 23 例(46.9%)、15 例(30.7%)和 11 例(22.4%)。39 例(76.5%)患者在 CR1 时接受了异基因 SCT。中位随访 54 个月后,所有患者的 4 年累积复发率和无病生存率(DFS)率分别为 30.0%和 52.0%,在 CR1 时接受异基因 SCT 的患者的相应结果分别为 20.5%和 64.1%。不良分子反应者的复发和 DFS 风险高于早期稳定分子反应者。

结论

这种基于 dasatinib 的方案在 Ph 阳性 ALL 成人患者中可有效实现良好的分子缓解和持久的 DFS。

试验注册

clinicaltrials.gov,NCT01004497。

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