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异基因干细胞移植后髓系白血病髓外复发为髓系肉瘤:预处理强度的影响

Extra-medullary recurrence of myeloid leukemia as myeloid sarcoma after allogeneic stem cell transplantation: impact of conditioning intensity.

作者信息

Frietsch Jochen J, Hunstig Friederike, Wittke Christoph, Junghanss Christian, Franiel Tobias, Scholl Sebastian, Hochhaus Andreas, Hilgendorf Inken

机构信息

Klinik für Innere Medizin II, Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Jena, Germany.

I. Medizinische Klinik und Poliklinik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Bone Marrow Transplant. 2021 Jan;56(1):101-109. doi: 10.1038/s41409-020-0984-4. Epub 2020 Jun 30.

DOI:10.1038/s41409-020-0984-4
PMID:32606455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7796857/
Abstract

Myeloid sarcoma (MS) as a solid extra-medullary (EM) manifestation of acute myeloid leukemia (AML), myeloproliferative or myelodysplastic syndromes is a rare presentation of relapse after allogeneic hematopoietic stem cell transplantation (HSCT). The databases of the Departments of Hematology and Oncology of the University Hospitals of Jena and Rostock were screened for patients aged 18 years or older for onset of MS after HSCT for myeloid malignancies between 2002 and 2019. Nineteen patients with MS were identified, the majority of whom had received reduced-intensity conditioning (RIC). The median onset of MS was 425 days after HSCT and the median overall survival since MS was 234 days. Although MS is associated with a poor prognosis, three patients survived more than two years and one more than 11 years after MS onset. These results indicate that RIC protocols may be associated with a higher risk of EM relapse. Since EM relapse occurred in the presence of Graft-versus-host-disease, these observations also demonstrate the limitations of graft-versus-tumor effects after HSCT. In conclusion, occurrence of MS after HSCT is associated with a poor prognosis, as multimodal curative concepts including intensive chemotherapy and another HSCT are often not viable.

摘要

髓系肉瘤(MS)作为急性髓系白血病(AML)、骨髓增殖性或骨髓增生异常综合征的一种实体性髓外(EM)表现,是异基因造血干细胞移植(HSCT)后复发的一种罕见表现。对耶拿和罗斯托克大学医院血液科和肿瘤科的数据库进行筛查,以寻找2002年至2019年间18岁及以上因髓系恶性肿瘤接受HSCT后发生MS的患者。共确定了19例MS患者,其中大多数接受了减低强度预处理(RIC)。MS的中位发病时间为HSCT后425天,自MS发生后的中位总生存期为234天。尽管MS预后较差,但有3例患者在MS发病后存活超过两年,1例存活超过11年。这些结果表明,RIC方案可能与EM复发风险较高有关。由于EM复发发生在存在移植物抗宿主病的情况下,这些观察结果也证明了HSCT后移植物抗肿瘤效应的局限性。总之,HSCT后发生MS与预后不良相关,因为包括强化化疗和再次HSCT在内的多模式治愈性概念往往不可行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3499/7796857/0003d9746836/41409_2020_984_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3499/7796857/0003d9746836/41409_2020_984_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3499/7796857/0003d9746836/41409_2020_984_Fig1_HTML.jpg

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