Department of Stem Cell Transplantation, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Department of Haematology, Vita-Salute San Raffaele University Milano, Milano, Italy.
Br J Haematol. 2019 Aug;186(3):484-489. doi: 10.1111/bjh.15952. Epub 2019 May 15.
Allogeneic stem cell transplantation (alloSCT) is a curative procedure for myelofibrosis. Elderly people are mainly affected, limiting the feasibility of myeloablative regimens. The introduction of reduced-intensity conditioning (RIC) made alloSCT feasible for older patients. Nevertheless, the incidence of myelofibrosis is not negligible in young patients, who are theoretically able to tolerate high-intensity therapy. Very few data are available about the efficacy of RIC-alloSCT in younger myelofibrosis patients. This study included 56 transplanted patients aged <55 years. Only 30% had a human leucocyte antigen (HLA)-matched sibling donor, the others were transplanted from a fully-matched (36%) or partially-matched (34%) unrelated donor. All transplants were conditioned according the European Society for Blood and Marrow Transplantation protocol: busulfan-fludarabine + anti-thymocyte globulin, followed by ciclosporin and mycophenolate. One patient experienced primary graft failure. Incidence of graft-versus-host disease grade II-IV was 44% (grade III/IV 23%). One-year non-relapse mortality was 7% and the 5-year cumulative incidence of relapse was 19%. After a median follow-up of 8·6 years, the estimated 5-year progression-free survival and overall survival (OS) was 68% and 82%, respectively. Patients with fully-matched donor had a 5-year OS of 92%, in contrast to 68% for those with a mismatched donor (P = 0·03). The most important outcome-determining factor is donor HLA-matching. In conclusion, RIC-alloSCT ensures optimal engraftment and low relapse rate in younger myelofibrosis patients, enabling the possibility of cure in this group.
异基因造血干细胞移植(alloSCT)是治疗骨髓纤维化的一种有治愈可能的方法。老年人受影响最大,限制了清髓性方案的可行性。减强度预处理(RIC)的引入使得 alloSCT 对老年患者变得可行。然而,年轻患者骨髓纤维化的发病率也不容忽视,他们理论上能够耐受高强度治疗。RIC-alloSCT 在年轻骨髓纤维化患者中的疗效数据非常有限。这项研究纳入了 56 名年龄<55 岁的移植患者。只有 30%的患者有人类白细胞抗原(HLA)匹配的同胞供者,其余的患者是从完全匹配(36%)或部分匹配(34%)的无关供者中移植的。所有的移植都按照欧洲血液和骨髓移植学会的方案进行预处理:白消安-氟达拉滨+抗胸腺细胞球蛋白,随后是环孢素和霉酚酸酯。1 例患者发生原发性移植物失败。Ⅱ-Ⅳ级移植物抗宿主病的发生率为 44%(Ⅲ/Ⅳ级 23%)。1 年非复发死亡率为 7%,5 年累积复发率为 19%。中位随访 8.6 年后,估计 5 年无进展生存率和总生存率(OS)分别为 68%和 82%。完全匹配供者的 5 年 OS 为 92%,而不匹配供者的 5 年 OS 为 68%(P=0.03)。最重要的预后决定因素是供者 HLA 匹配。总之,RIC-alloSCT 可确保年轻骨髓纤维化患者获得最佳的植入和低复发率,使该组患者有治愈的可能。