Kröger Nicolaus, Giorgino Toni, Scott Bart L, Ditschkowski Markus, Alchalby Haefaa, Cervantes Francisco, Vannucchi Alessandro, Cazzola Mario, Morra Enrica, Zabelina Tatjana, Maffioli Margherita, Pereira Arturo, Beelen Dietrich, Deeg H Joachim, Passamonti Francesco
Department of Stem Cell Transplantation, University Hospital Hamburg, Hamburg, Germany;
Institute of Neurosciences, National Research Council of Italy, Padova, Italy;
Blood. 2015 May 21;125(21):3347-50; quiz 3364. doi: 10.1182/blood-2014-10-608315. Epub 2015 Mar 17.
Allogeneic hematopoietic stem cell transplantation (SCT) is the only curative option for patients with primary myelofibrosis (PMF), but information on its net advantage over conventional therapies is lacking. Using ad hoc statistical analysis, we determined outcomes in 438 patients <65 years old at diagnosis who received allogenic SCT (n = 190) or conventional therapies (n = 248). Among patients at low risk per the Dynamic International Prognostic Scoring System (DIPSS) model, the relative risk of death after allogenic SCT vs those treated with nontransplant modalities was 5.6 (95% CI, 1.7-19; P = .0051); for intermediate-1 risk it was 1.6 (95% CI, 0.79-3.2; P = .19), for intermediate-2 risk, 0.55 (95% CI, 0.36-0.83; P = .005), and for high risk, 0.37 (95% CI, 0.21-0.66; P = .0007). Thus, patients with intermediate-2 or high-risk PMF clearly benefit from allogenic SCT. Patients at low risk should receive nontransplant therapy, whereas individual counseling is indicated for patients at intermediate-1 risk.
异基因造血干细胞移植(SCT)是原发性骨髓纤维化(PMF)患者唯一的治愈选择,但缺乏其相对于传统疗法的净优势的相关信息。通过专门的统计分析,我们确定了438例诊断时年龄<65岁、接受异基因SCT(n = 190)或传统疗法(n = 248)的患者的结局。根据动态国际预后评分系统(DIPSS)模型,低风险患者中,异基因SCT后死亡的相对风险与接受非移植治疗的患者相比为5.6(95%CI,1.7 - 19;P = 0.0051);中-1风险患者为1.6(95%CI,0.79 - 3.2;P = 0.19),中-2风险患者为0.55(95%CI,0.36 - 0.83;P = 0.005),高风险患者为0.37(95%CI,0.21 - 0.66;P = 0.0007)。因此,中-2或高风险的PMF患者显然从异基因SCT中获益。低风险患者应接受非移植治疗,而中-1风险患者则需进行个体化咨询。