Haematology, Policlinico Hospital, Bari, Italy.
Haematology, "G.Moscati" Hospital, Taranto, Italy.
Clin Lymphoma Myeloma Leuk. 2019 Jan;19(1):35-40. doi: 10.1016/j.clml.2018.08.012. Epub 2018 Sep 12.
Hodgkin lymphoma (HL) is a potentially curable disease, and modern therapy is expected to successfully cure more than 80% of the patients. However, patients progressing after intensive treatments, such as autologous stem cell transplantation (SCT), have a very poor outcome. Allogeneic SCT offers the only strategy with a curative potential for these patients. This study reports a retrospective multicenter experience of the Rete Ematologica Pugliese (REP) over the past 17 years, aiming to define the impact of each patient's disease and transplant-related characteristics on outcomes.
We retrospectively studied 72 patients with HL who received allogeneic SCT from 2000 to 2017. At the time of allogeneic SCT, 33 (46%) patients had chemosensitive disease, and 39 (54%) were chemo-refractory. All patients received reduced-intensity conditioning, 50% received grafts from a matched sibling donor, and 50% from a matched-unrelated donor.
With a median follow-up of 48 months (range, 3-195 months), 30 patients are alive, and 42 have died. The Kaplan-Meier estimates of overall survival and progression-free survival at 5 years were 35% and 34%, respectively. Following transplantation, 12 (17%) patients died of non-relapse mortality at a median of 90 days (range, 1 day-20 months). The causes of death included infection (n = 7), graft-versus-host disease (n = 3), and multi-organ failure (n = 2).
Allogeneic SCT results extend survival in selected patients with relapsed/refractory HL, showing low treatment-related mortality. Patients with active disease at the time of allogeneic transplantation have poor outcomes. Allogeneic SCT may be an effective salvage strategy for patients who relapse after an autologous SCT.
霍奇金淋巴瘤(HL)是一种潜在可治愈的疾病,现代疗法有望成功治愈超过 80%的患者。然而,经过强化治疗(如自体干细胞移植[SCT])后进展的患者预后非常差。异基因 SCT 是这些患者唯一具有治愈潜力的策略。本研究报告了过去 17 年里 Pugliese 血液学网络(REP)的一项回顾性多中心经验,旨在确定每位患者疾病和移植相关特征对结局的影响。
我们回顾性研究了 2000 年至 2017 年期间接受异基因 SCT 的 72 例 HL 患者。在进行异基因 SCT 时,33 例(46%)患者疾病对化疗敏感,39 例(54%)患者对化疗耐药。所有患者均接受了强度降低的预处理,50%的患者接受了亲缘相合供者的移植物,50%的患者接受了亲缘无关供者的移植物。
中位随访 48 个月(范围,3-195 个月),30 例患者存活,42 例患者死亡。5 年时的总生存率和无进展生存率的 Kaplan-Meier 估计值分别为 35%和 34%。移植后,12 例(17%)患者因非复发相关死亡,中位时间为 90 天(范围,1 天-20 个月)。死亡原因包括感染(n=7)、移植物抗宿主病(n=3)和多器官衰竭(n=2)。
异基因 SCT 可延长复发/难治性 HL 患者的生存时间,且治疗相关死亡率较低。在进行异基因移植时患有活动性疾病的患者结局较差。异基因 SCT 可能是自体 SCT 后复发患者的有效挽救策略。