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二线和三线挽救性化疗后行异基因干细胞移植可使原发性难治性急性髓系白血病患者获得高生存率——一项基于人群的研究

Second- and Third-Line Salvage Chemotherapy Followed by Allogeneic Stem Cell Transplantation Leads to High Survival Rates in Primary Refractory AML-A Population-Based Study.

作者信息

Liew-Littorin Markus, Deleskog-Spångberg Linn, Deneberg Stefan, Janosi Judit, Lazarevic Vladimir, Nilsson Gustav, Papageorgiou Aristea, Robelius Anna, Vennström Lovisa, Juliusson Gunnar, Uggla Bertil, Höglund Martin, Lehmann Sören

机构信息

Department of Medicine, Division of Hematology, Örebro University Hospital, Örebro, Sweden.

School of Medical Sciences, Örebro University, Örebro, Sweden.

出版信息

Eur J Haematol. 2025 Oct;115(4):423-432. doi: 10.1111/ejh.70009. Epub 2025 Jul 24.

Abstract

Refractory acute myeloblastic leukemia (AML) is poorly studied. In this study, we characterized primary refractory AML and investigated treatment and outcome in a population-based setting. Based on all AML patients receiving intensive induction therapy at 12 Swedish hospitals from 2011 to 2018 (N = 1221), we identified 306 patients that failed to achieve composite complete remission (CRc) after first-line therapy. Two-hundred-sixteen (71%) of these patients received salvage treatment with intensive chemotherapy (ICT), of which 126 (58%) achieved CRc and 85 (39%) underwent allogeneic stem cell transplantation (HSCT). One- and 3-year overall survival (OS) in patients receiving salvage ICT were 56.8% and 28.9%, respectively. Secondary AML and adverse ELN risk were associated with worse OS after salvage ICT, while fludarabine-based FAIDA versus amsacrine-based ACE salvage and HSCT were associated with better OS. Three-year OS after first or second salvage chemotherapy, followed by HSCT were 55% and 71%, respectively. Refractory patients responding to salvage ICT showed only a nonsignificant trend toward inferior OS compared to patients in CRc after the first cycle. In conclusion, refractory AML patients eligible for further intensive therapy have a reasonable chance of obtaining remission and long-term survival when followed by HSCT. The results can serve as a basis for evaluation of new treatments in refractory AML.

摘要

难治性急性髓系白血病(AML)的研究较少。在本研究中,我们对原发性难治性AML进行了特征描述,并在基于人群的环境中调查了治疗情况和预后。基于2011年至2018年在瑞典12家医院接受强化诱导治疗的所有AML患者(N = 1221),我们确定了306例一线治疗后未达到完全缓解(CRc)的患者。其中216例(71%)患者接受了强化化疗(ICT)挽救治疗,其中126例(58%)达到CRc,85例(39%)接受了异基因干细胞移植(HSCT)。接受挽救性ICT治疗的患者1年和3年总生存率(OS)分别为56.8%和28.9%。继发性AML和不良欧洲白血病网络(ELN)风险与挽救性ICT治疗后的较差OS相关,而基于氟达拉滨的FAIDA方案与基于安吖啶的ACE挽救方案及HSCT与较好的OS相关。首次或第二次挽救化疗后接受HSCT的患者3年OS分别为55%和71%。与第一个周期后达到CRc的患者相比,对挽救性ICT有反应的难治性患者的OS仅呈现出不显著的劣势趋势。总之,有资格接受进一步强化治疗的难治性AML患者在接受HSCT后有合理的机会获得缓解和长期生存。这些结果可作为评估难治性AML新治疗方法的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afae/12402835/16b9595ed137/EJH-115-423-g004.jpg

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