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自体造血干细胞移植治疗低危急性髓系白血病:单中心经验与当前挑战

Autologous stem cell transplantation in favorable-risk acute myeloid leukemia: single-center experience and current challenges.

机构信息

Hematology, Department of Translational and Precision Medicine, Sapienza University Policlinico Umberto I, Via Benevento 6, 00161, Rome, Italy.

Department of Immunohematology and Transfusional Medicine, AOU Policlinico Umberto I, Rome, Italy.

出版信息

Int J Hematol. 2022 Oct;116(4):586-593. doi: 10.1007/s12185-022-03370-4. Epub 2022 May 13.

Abstract

BACKGROUND

Autologous stem cell transplantation (ASCT) has gained growing consideration as a treatment option for favorable-risk acute myeloid leukemia (FR-AML) in first complete remission (CR1), compared with chemotherapy.

MATERIALS AND METHODS

We report the long-term outcomes of 117 consecutive patients with FR-AML fit for intensive chemotherapy diagnosed in our center between 1999 and 2020, who underwent ASCT.

RESULTS

Sixty-five of the 117 were eligible for intensive post-remission treatment, and 42 of those 65 received ASCT. Median follow up was 132 months. Overall survival (OS) and disease-free survival (DFS) were 75% and 76%. Higher doses of CD34 + stem cell infusions negatively impacted DFS in multivariate analysis. Core-binding factor (CBF) leukemia was an independent prognostic factor for improved DFS. No differences based on pre-transplant measurable residual disease (MRD) were observed. In CBF leukemia, 10-year DFS is 72% for MRD-positive patients versus 100% for MRD negative patients.

CONCLUSIONS

ASCT is effective and safe in FR-AML patients. In CBF leukemia, ASCT provides excellent results regardless of achievement of bone marrow MRD negativity. In NPM1-mutated/FLT3-wild type (mNPM1) AML, early molecular response seems to have more impact on prognosis. Prospective investigation of the role of gemtuzumab ozogamicin in this setting is ongoing.

摘要

背景

与化疗相比,自体干细胞移植(ASCT)作为首次完全缓解(CR1)时低危急性髓系白血病(FR-AML)的治疗选择得到了越来越多的关注。

材料与方法

我们报告了 1999 年至 2020 年期间在本中心诊断为 FR-AML 且适合强化化疗的 117 例连续患者接受 ASCT 的长期结果。

结果

117 例中有 65 例符合强化缓解后治疗标准,其中 42 例接受 ASCT。中位随访时间为 132 个月。总生存(OS)和无病生存(DFS)分别为 75%和 76%。多变量分析显示,CD34+干细胞输注剂量越高,DFS 越差。核心结合因子(CBF)白血病是 DFS 改善的独立预后因素。未观察到基于移植前可测量残留疾病(MRD)的差异。在 CBF 白血病中,MRD 阳性患者的 10 年 DFS 为 72%,而 MRD 阴性患者为 100%。

结论

ASCT 对 FR-AML 患者有效且安全。在 CBF 白血病中,无论骨髓 MRD 是否为阴性,ASCT 均可提供良好的结果。在 NPM1 突变/FLT3 野生型(mNPM1)AML 中,早期分子反应似乎对预后有更大影响。正在进行前瞻性研究 gemtuzumab ozogamicin 在该环境中的作用。

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