Cahu X, Chevallier P, Clavert A, Suarez F, Michallet M, Vincent L, Vigouroux S, Blaise D, Mariette C, Bilger K, Robin M, Yakoub-Agha I, Peffault de Latour R, Mohty M
Hématologie Clinique, CHU Rennes, Hôpital Pontchaillou, Rennes, France.
Hématologie Clinique, CHU Nantes, Hôtel Dieu, Nantes, France.
Bone Marrow Transplant. 2014 Jun;49(6):756-60. doi: 10.1038/bmt.2014.31. Epub 2014 Mar 10.
Progression of Philadelphia-negative myeloproliferative (MPN) or myelodysplastic/myeloproliferative neoplasms (MDS/MPN) to acute myeloid leukemia (AML) is an adverse event in the course of the disease. Although allogeneic hematopoietic SCT (allo-SCT) is considered as the only curative therapy, few data exist on the outcome of patients with Philadelphia-negative MPN or MDS/MPN in blast phase who received an allo-SCT. Sixty patients were included in this retrospective study. AML was secondary to an MPN in 43 cases, whereas AML evolved from an MDS/MPN in 17 cases. Patients received allo-SCT in CR or advanced disease in 26 cases and 34 cases, respectively. With a median follow-up of 31 months (range, 25-44), OS and leukemia-free survival (LFS) were, respectively, 18% and 9% at 3 years. CR at transplant was associated with an improved LFS in univariate and multivariate analysis. The 3-year LFS was 18% for patients undergoing allo-SCT in CR versus 3% in advanced disease (P=0.008). Absence of thrombosis and an intermediate or favorable AML karyotype were associated with an improved outcome for patients who received allo-SCT in CR. New strategies are needed to improve the outcome of patients with MPN-MDS/MPN in blast phase.
费城染色体阴性骨髓增殖性肿瘤(MPN)或骨髓增生异常/骨髓增殖性肿瘤(MDS/MPN)进展为急性髓系白血病(AML)是疾病过程中的不良事件。尽管异基因造血干细胞移植(allo-SCT)被认为是唯一的治愈性疗法,但关于处于原始细胞期的费城染色体阴性MPN或MDS/MPN患者接受allo-SCT后的结局数据很少。本回顾性研究纳入了60例患者。43例AML继发于MPN,而17例AML由MDS/MPN演变而来。患者分别在完全缓解(CR)期或疾病进展期接受allo-SCT,其中26例处于CR期,34例处于疾病进展期。中位随访时间为31个月(范围25 - 44个月),3年总生存期(OS)和无白血病生存期(LFS)分别为18%和9%。在单因素和多因素分析中,移植时处于CR期与改善的LFS相关。处于CR期接受allo-SCT的患者3年LFS为18%,而处于疾病进展期的患者为3%(P = 0.008)。对于在CR期接受allo-SCT的患者,无血栓形成以及AML核型为中间型或良好型与较好的结局相关。需要新的策略来改善处于原始细胞期的MPN - MDS/MPN患者的结局。