Machherndl-Spandl Sigrid, Hannouf Sarah, Nikoloudis Alexander, Zach Otto, Strassl Irene, Kaynak Emine, Webersinke Gerald, Gruber-Rossipal Christine, Rumpold Holger, Schimetta Wolfgang, Clausen Johannes, Buxhofer-Ausch Veronika
Department of Internal Medicine I: Hematology with Stem-Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz-Elisabethinen, 4020 Linz, Austria.
Medical Faculty, Johannes Kepler University, 4020 Linz, Austria.
Cancers (Basel). 2024 Sep 25;16(19):3257. doi: 10.3390/cancers16193257.
(1) Background: Allogeneic hematopoietic stem-cell transplantation (allo-HSCT) is the only treatment with the potential for cure in patients with myelofibrosis (MF). However, the risk of graft rejection, which is particularly high in MF, and the risk of significant non-relapse mortality must be considered. (2) Methods: In this retrospective, single-center study, we compared allo-HSCT outcomes in 36 adult patients with MF transplanted at two-time intervals (2001-2015 versus 2016-2021). (3) Results: The estimated median overall survival was 48.9 months (95%CI 0.00-98.2) in the cohort transplanted before 2016 and not reached in the more recent years ( = 0.04) due to markedly lower non-relapse mortality ( = 0.02). The 3-year relapse incidence was low in both cohorts (11.1% and 12.5%, > 0.99). When comparing only subgroups within the more recent cohort based on the presence or absence of total body irradiation (TBI) or the use of sequential regimens, OS and PFS were comparable. (4) Conclusion: Pretreatment with ruxolitinib, intensified conditioning, and the preferential use of haploidentical related instead of mismatched unrelated donors for patients lacking an HLA-identical donor are most likely responsible for the improved outcome after allo-HCT in MF in recent years.
(1) 背景:异基因造血干细胞移植(allo-HSCT)是骨髓纤维化(MF)患者唯一有可能治愈的治疗方法。然而,必须考虑移植排斥风险,这在MF患者中尤为高,以及显著的非复发死亡率风险。(2) 方法:在这项回顾性单中心研究中,我们比较了36例成年MF患者在两个时间段(2001 - 2015年与2016 - 2021年)进行allo-HSCT的结果。(3) 结果:2016年前移植的队列中,估计中位总生存期为48.9个月(95%CI 0.00 - 98.2),而近年来未达到(P = 0.04),原因是非复发死亡率显著降低(P = 0.02)。两个队列的3年复发率均较低(分别为11.1%和12.5%,P > 0.99)。在仅比较最近队列中基于是否进行全身照射(TBI)或使用序贯方案的亚组时,总生存期(OS)和无进展生存期(PFS)具有可比性。(4) 结论:近年来,芦可替尼预处理、强化预处理方案以及对于缺乏HLA相合同胞供者的患者优先使用单倍体相关供者而非不匹配的无关供者,很可能是MF患者allo-HCT后预后改善的原因。