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一项比较干细胞移植与传统疗法治疗低危和中危骨髓增生异常综合征患者的随机研究。

A Randomized Study Comparing Stem Cell Transplantation Versus Conventional Therapy for Low- and Intermediate-Risk Myelodysplastic Syndromes Patients.

作者信息

Yu Zheng-Ping, Ding Jia-Hua, Sun Ai-Ning, Ge Zheng, Chen Bao-An, Wu De-Pei

机构信息

1 Hematology Division, The First Affiliated Hospital of Soochow University , Suzhou, China .

2 Department of Hematology (Key Department of Jiangsu Medicine), ZhongDa Hospital, Southeast University , Nanjing, China .

出版信息

Stem Cells Dev. 2017 Aug 1;26(15):1132-1139. doi: 10.1089/scd.2017.0031. Epub 2017 Jun 12.

Abstract

The treatment of myelodysplastic syndromes (MDS) involves improving patient survival and quality of life (QoL) and decreasing the likelihood of progression to AML. Although the treatment outcomes of MDS remain unsatisfactory, few comparative studies have been performed while comparing the outcomes of low-risk and intermediate-risk patients treated with supportive care and chemotherapeutics to those of patients treated with allogeneic hematopoietic stem cell transplantation (allo-HSCT). Therefore, we designed a clinical control study to compare the outcomes of supportive care and chemotherapeutics versus allo-HSCT treatment in MDS patients. A total of 182 patients with MDS were enrolled in the study, including 91 in the no-HSCT (control) group and 91 in the allo-HSCT group. The complete remission (CR) rate in the allo-HSCT group was significantly higher than that in the control group (53.8% vs. 33.0%; P < 0.05). The QoL of patients in the HSCT group was much higher than that in the control group (53.8% vs. 37.4%; P < 0.05). The overall survival (OS) rates were 79.0% and 56.0% (P < 0.05) in the HSCT group and the control group, respectively. In conclusion, a high-dose fludarabine (Flu), busulfan (Bu), cyclophosphamide (CTX)-based conditioning regimen was well tolerated and significantly speeded hematopoietic recovery. In addition, this regimen increased procedure-related toxicity and improved QoL and OS.

摘要

骨髓增生异常综合征(MDS)的治疗旨在提高患者生存率和生活质量(QoL),并降低进展为急性髓系白血病(AML)的可能性。尽管MDS的治疗效果仍不尽人意,但在比较接受支持治疗和化疗的低风险及中风险患者与接受异基因造血干细胞移植(allo-HSCT)患者的治疗结果方面,很少有对比研究。因此,我们设计了一项临床对照研究,以比较MDS患者接受支持治疗和化疗与allo-HSCT治疗的结果。共有182例MDS患者纳入本研究,其中非HSCT(对照)组91例,allo-HSCT组91例。allo-HSCT组的完全缓解(CR)率显著高于对照组(53.8%对33.0%;P < 0.05)。HSCT组患者的生活质量远高于对照组(53.8%对37.4%;P < 0.05)。HSCT组和对照组的总生存率(OS)分别为79.0%和56.0%(P < 0.05)。总之,基于大剂量氟达拉滨(Flu)、白消安(Bu)、环磷酰胺(CTX)的预处理方案耐受性良好,显著加速了造血恢复。此外,该方案增加了与治疗相关的毒性,但改善了生活质量和总生存率。

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