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挽救性异基因干细胞移植在自体干细胞移植后复发的急性髓系白血病患者中的可行性和疗效

Feasibility and efficacy of salvage allogeneic stem cell transplantation in AML patients relapsing after autologous stem cell transplantation.

作者信息

Shumilov Evgenii, Shakhanova Inna, Flach Johanna, Schmidt Nicole, Buerki Susanne, Legros Myriam, Kronig Marie-Noëlle, Ofran Yishai, Gerull Sabine, Medinger Michael, Taleghani Behrouz Mansouri, Passweg Jakob, Halter Jörg, Bacher Ulrike, Pabst Thomas

机构信息

Department of Medical Oncology, Inselspital, Bern University Hospital, Bern, Switzerland.

Department of Hematology and Medical Oncology, University Medicine Göttingen (UMG), Göttingen, Germany.

出版信息

Bone Marrow Transplant. 2022 Feb;57(2):224-231. doi: 10.1038/s41409-021-01521-5. Epub 2021 Nov 13.

Abstract

Autologous hematopoietic cell transplantation (HCT) is suitable for consolidation of favorable-/intermediate-risk AML patients in CR1. However, ~50% of AML patients relapse after autologous HCT, and efficacy of subsequent salvage strategies including allogeneic HCT remains unclear. We studied 123 consecutive patients with newly diagnosed AML undergoing high-dose chemotherapy (HDCT)/autologous HCT in CR1. In relapsing patients afterwards, we analyzed salvage treatments and outcomes focusing particularly on salvage allogeneic HCT. Of 123 patients, 64 (52%) relapsed after autologous HCT. Subsequently, 13 (21%) received palliative therapy, whereas 51 (79%) proceeded to salvage therapy with a curative intent. Of the 47 patients with a curative intent and who did not proceed directly to allogeneic HCT, 23 (49%) achieved CR2 or had ongoing hematologic CR1 despite molecular relapse. Finally, 30 patients (47%) received allogeneic HCT with estimated 3-year leukemia-free and overall survival rates of 33% and 43%. Hematologic remission at allogeneic HCT and lack of acute GvHD had a positive impact on OS and LFS (p < 0.05). Our study suggests that almost 80% of AML patients can undergo salvage therapy following relapse after front-line HDCT/autologous HCT. Allogeneic HCT can provide cure in one third of patients relapsing after front-line HDCT/autologous HCT.

摘要

自体造血细胞移植(HCT)适用于处于完全缓解期(CR1)的低危/中危急性髓系白血病(AML)患者的巩固治疗。然而,约50%的AML患者在自体HCT后复发,包括异基因HCT在内的后续挽救策略的疗效仍不明确。我们研究了123例连续的新诊断AML患者,这些患者在CR1期接受了大剂量化疗(HDCT)/自体HCT。在随后复发的患者中,我们分析了挽救治疗及结果,尤其关注挽救性异基因HCT。123例患者中,64例(52%)在自体HCT后复发。随后,13例(21%)接受了姑息治疗,而51例(79%)进行了旨在治愈的挽救治疗。在47例有治愈意图且未直接进行异基因HCT的患者中,23例(49%)达到了第二次完全缓解(CR2)或尽管有分子复发但仍处于持续的血液学CR1状态。最后,30例患者(47%)接受了异基因HCT,估计3年无白血病生存率和总生存率分别为33%和43%。异基因HCT时的血液学缓解及无急性移植物抗宿主病(GvHD)对总生存期(OS)和无白血病生存期(LFS)有积极影响(p<0.05)。我们的研究表明,几乎80%的AML患者在一线HDCT/自体HCT后复发可接受挽救治疗。异基因HCT可为三分之一的一线HDCT/自体HCT后复发的患者提供治愈机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a605/8821015/2659e355886a/41409_2021_1521_Fig1_HTML.jpg

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