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异基因造血干细胞移植前两种基于氟达拉滨的减低强度预处理方案的比较:与氟达拉滨/白消安相比,氟达拉滨/美法仑与更高的急性移植物抗宿主病发生率和非复发死亡率以及更低的复发率相关。

Comparison between two fludarabine-based reduced-intensity conditioning regimens before allogeneic hematopoietic stem-cell transplantation: fludarabine/melphalan is associated with higher incidence of acute graft-versus-host disease and non-relapse mortality and lower incidence of relapse than fludarabine/busulfan.

作者信息

Shimoni A, Hardan I, Shem-Tov N, Rand A, Herscovici C, Yerushalmi R, Nagler A

机构信息

The Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel.

出版信息

Leukemia. 2007 Oct;21(10):2109-16. doi: 10.1038/sj.leu.2404886. Epub 2007 Aug 9.

DOI:10.1038/sj.leu.2404886
PMID:17690701
Abstract

Reduced-intensity conditioning (RIC) regimens are increasingly used in allogeneic stem-cell transplantation (SCT). There are no data whether any of these regimens has advantage and in what setting. We retrospectively analyzed SCT outcomes in 151 patients given fludarabine-based RIC for various hematological malignancies; 72 conditioned with fludarabine and intravenous-busulfan (FB) and 79 with fludarabine and melphalan (FM). FM was more myelosuppressive. Grade III-IV organ toxicity occurred in 31 and 53% of FB and FM recipients (P=0.005) and acute graft-versus-host disease grade II-IV in 33 and 53%, respectively (P=0.01). Non-relapse mortality rate (NRM) was 16 and 40%, respectively (P=0.003). Active disease (HR 2.2, P=0.003) and prior autologous SCT (HR 1.7, P=0.04) predicted inferior overall survival (OS). Among patients transplanted in remission, OS was 72 and 36% after FB and FM, respectively (P=0.03) due to increased NRM with FM. Similarly, patients transplanted in active disease experienced higher NRM with FM, however lower relapse rates resulted in equivalent OS. In conclusion, there are marked differences in outcome between RIC regimens that are theoretically dose-equivalent. The FM regimen is more myelosuppressive and toxic but controls disease better. FB was associated with improved survival in patients transplanted in remission. These observations merit further study in prospective studies.

摘要

减低强度预处理(RIC)方案在异基因干细胞移植(SCT)中越来越常用。目前尚无数据表明这些方案中是否有任何一种具有优势以及在何种情况下具有优势。我们回顾性分析了151例接受基于氟达拉滨的RIC方案治疗各种血液系统恶性肿瘤患者的SCT结果;72例接受氟达拉滨和静脉白消安(FB)预处理,79例接受氟达拉滨和美法仑(FM)预处理。FM的骨髓抑制作用更强。FB和FM接受者中分别有31%和53%发生III - IV级器官毒性(P = 0.005),急性移植物抗宿主病II - IV级分别为33%和53%(P = 0.01)。非复发死亡率(NRM)分别为16%和40%(P = 0.003)。疾病活动期(HR 2.2,P = 0.003)和既往自体SCT(HR 1.7,P = 0.04)预示总体生存率(OS)较差。在缓解期移植的患者中,FB和FM后的OS分别为72%和36%(P = 0.03),原因是FM组NRM增加。同样,处于疾病活动期移植的患者FM组NRM更高,但复发率较低导致OS相当。总之,理论上剂量等效的RIC方案在结局上存在显著差异。FM方案骨髓抑制作用更强且毒性更大,但对疾病的控制更好。FB与缓解期移植患者的生存率提高相关。这些观察结果值得在前瞻性研究中进一步探讨。

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