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Allogeneic hemopoietic SCT for patients with primary myelofibrosis: a predictive transplant score based on transfusion requirement, spleen size and donor type.

机译:原发性骨髓纤维化患者的异基因造血SCT:基于输血需求,脾脏大小和供体类型的预测移植评分。

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A total of 46 patients with primary myelofibrosis (PMF) (median age 51 years), underwent an allogeneic hemopoietic SCT (HSCT) after a thiotepa-based reduced-intensity conditioning regimen. The median follow-up for surviving patients is 3.8 years. In multivariate analysis, independent unfavorable factors for survival were RBC transfusions >20, a spleen size >22 cm and an alternative donor-24 patients had 0-1 unfavorable predictors (low risk) and 22 patients had 2 or more negative predictors (high risk). The overall actuarial 5-year survival of the 46 patients is 45%. The actuarial survival of low-risk and high-risk patients is, respectively, 77 and 8% (P<0.0001); this is because of a higher TRM for high-risk patients (RR, 6.0, P=0.006) and a higher relapse-related death (RR, 7.69; P=0.001). In multivariate Cox analysis, the score maintained its predictive value (P=0.0003), even after correcting for donor-patient age and gender, Dupriez score, IPSS (International Prognostic Scoring System) score pre-transplant and splenectomy. In conclusion, PMF patients undergoing an allogeneic HSCT may be scored according to the spleen size, transfusion history and donor type; this scoring system may be useful to discuss transplant strategies.
机译:总共46例原发性骨髓纤维化(PMF)患者(中位年龄51岁)在接受基于thiotepa的强度降低调理方案后接受了异基因造血SCT(HSCT)。存活患者的中位随访时间为3.8年。在多因素分析中,生存的独立不利因素是:RBC输血> 20,脾脏大小> 22 cm和供体替代者24例患者有0-1个不利预测因素(低风险)和22例患者有2个或更多阴性预测因素(高风险) )。 46名患者的总精算5年生存率为45%。低危和高危患者的精算生存率分别为77%和8%(P <0.0001)。这是因为高危患者的TRM较高(RR,6.0,P = 0.006)和较高的复发相关死亡(RR,7.69; P = 0.001)。在多变量Cox分析中,即使在校正供体患者的年龄和性别,Dupriez评分,IPSS(国际预后评分系统)评分(移植前和脾切除术)后,评分仍保持其预测值(P = 0.0003)。总之,接受异基因HSCT的PMF患者可根据脾脏大小,输血史和供体类型进行评分。该评分系统可能有助于讨论移植策略。

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