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同种异体造血干细胞移植和移植前策略在 NPM1 突变型急性髓系白血病患者中的应用:单中心经验。

Allogeneic hematopoietic stem cell transplantation and pre-transplant strategies in patients with NPM1-mutated acute myeloid leukemia: a single center experience.

机构信息

Department of Hematology, Oncology and Clinical Immunology, Heinrich-Heine-University, Medical Faculty, Moorenstr. 5, 40225, Düsseldorf, Germany.

Department of Hematology and Stem Cell Transplantation, University Hospital Essen, Essen, Germany.

出版信息

Sci Rep. 2023 Jul 4;13(1):10774. doi: 10.1038/s41598-023-38037-5.

Abstract

Patients with acute myeloid leukemia (AML) and nucleophosmin 1 gene mutations (NPM1) show a favorable prognosis with chemotherapy (CT) in the absence of negative prognostic genetic abnormalities. Between 2008 and 2021 64 patients with NPM1AML received alloHSCT because of additional adverse prognostic factors (1st line), inadequate response to or relapse during or after CT (2nd line). To expand the evidence in alloTX in NPM1 AML, clinical and molecular data were retrospectively analyzed with respect to pre-transplant strategies and outcome. Patients with minimal residual disease negative (MRD-) CR at transplant had better 2-y-PFS and 2-y-OS (77% and 88%) than patients with minimal residual disease positive (MRD+) CR (41% and 71%) or patients with active disease (AD) at transplant (20% and 52%). The 2nd line patients with relapse after completing CT responded well to high dose cytarabine based salvage chemotherapy (salvage CT) in contrast to patients relapsing while still on CT (90% vs 20%, P = 0.0170). 2-y-PFS and 2-y-OS was 86% in patients who achieved a 2nd MRD- CR pre alloHSCT. Outcome in NPM1AML depends on disease burden at alloHSCT. Time and type of relapse in relation to CT are predictive for response to salvage CT.

摘要

患有急性髓细胞白血病(AML)和核磷蛋白 1 基因突变(NPM1)的患者在无不良预后遗传异常的情况下,化疗(CT)无不良预后。2008 年至 2021 年间,由于存在其他不良预后因素(一线)、CT 期间或之后反应不足或复发(二线),64 名 NPM1AML 患者接受了同种异体 HSCT。为了扩大 NPM1AML 中同种异体 TX 的证据,回顾性分析了与移植前策略和结果相关的临床和分子数据。移植时达到微小残留病阴性(MRD-)完全缓解(CR)的患者,其 2 年无进展生存(PFS)率和 2 年总生存(OS)率(分别为 77%和 88%)明显优于微小残留病阳性(MRD+)CR(分别为 41%和 71%)或移植时处于活动疾病(AD)的患者(分别为 20%和 52%)。与仍在接受 CT 治疗的患者相比,完成 CT 后复发的二线患者对基于高剂量阿糖胞苷的挽救性化疗(挽救性 CT)反应良好(分别为 90%和 20%,P=0.0170)。在同种异体 HSCT 前获得第二次 MRD-CR 的患者,其 2 年 PFS 和 2 年 OS 率为 86%。NPM1AML 的预后取决于同种异体 HSCT 时的疾病负担。与 CT 相关的复发时间和类型可预测挽救性 CT 的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c48d/10319811/5734c96ba8a5/41598_2023_38037_Fig1_HTML.jpg

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