首页> 外文期刊>Bone marrow transplantation >Feasibility of allo-SCT after hypomethylating therapy with decitabine for myelodysplastic syndrome.
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Feasibility of allo-SCT after hypomethylating therapy with decitabine for myelodysplastic syndrome.

机译:地西他滨低甲基化治疗骨髓增生异常综合症后进行allo-SCT的可行性。

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摘要

Decitabine is a hypomethylating agent with activity in myelodysplastic syndrome (MDS). It is largely unknown whether treatment with this drug before allo-SCT will increase the toxicity of the preparative regimen or otherwise affect the results of the transplant. We report the outcome of 17 patients with MDS with a median age of 55.5 years (range, 36-66 years) who underwent an allo-SCT (12 siblings, 5 unrelated) after prior therapy with decitabine. Preparative regimens consisted of fludarabine in combination with BU (n=8) or melphalan (n=9). The source of stem cells was marrow in four patients and peripheral blood (PB) in 13 patients. Thirteen patients were in CR within 100 days of transplant. With a median follow-up of 12 months (range, 3-35 months), 11 patients are alive; eight in CR and three with progressive disease. Prior therapy with hypomethylating agents did not increase toxicity and may improve the outcome of allogeneic transplant in MDS and should be evaluated in a prospective trial.
机译:地西他滨是在骨髓增生异常综合症(MDS)中具有活性的次甲基化剂。在异源SCT之前用这种药物进行治疗会增加制备方案的毒性,还是会影响移植结果,这在很大程度上是未知的。我们报告了17例中位年龄为55.5岁(范围36-66岁)的MDS患者在接受地西他滨治疗后接受了同种SCT(12例兄弟姐妹,5例无关)的结果。制备方案由氟达拉滨联合BU(n = 8)或美法仑(n = 9)组成。干细胞的来源为4名患者的骨髓和13名患者的外周血(PB)。移植后100天内有13例患者处于CR中。中位随访期为12个月(范围3-35个月),有11名患者还活着。 CR中有8名,有进行性疾病。先前使用次甲基化剂进行的治疗不会增加毒性,并且可能会改善MDS同种异体移植的结果,应在前瞻性试验中进行评估。

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