Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, California.
Department of Computational and Quantitative Medicine, City of Hope, Duarte, California.
Biol Blood Marrow Transplant. 2019 Dec;25(12):2383-2387. doi: 10.1016/j.bbmt.2019.07.041. Epub 2019 Aug 5.
Standard therapy for relapsed or refractory (rel/ref) primary mediastinal large B cell lymphoma (PMBCL) is salvage therapy followed by autologous (auto) hematopoietic stem cell transplantation (HSCT). However, many patients have refractory disease and are unable to undergo autoHSCT, and a sizeable proportion of patients will relapse after autoHSCT. By analogy to diffuse large B cell lymphoma, these patients may be treated with allogeneic (allo) HSCT with curative intent, but at the risk of significant morbidity and mortality. Given the advent of effective immunotherapy approaches for rel/ref PMBCL, it is important to better understand the toxicity and efficacy of alloHSCT in these patients, to which these new approaches could be an alternative. Therefore, we retrospectively studied the outcomes of alloHSCT in a multicenter cohort of 28 patients with rel/ref PMBCL who underwent transplantation at 4 centers. Most patients (79%) were sensitive to pretransplantation therapy and 86% received reduced-intensity conditioning. The overall progression-free survival (PFS), overall survival (OS), and cumulative incidences of nonrelapse mortality and relapse in the cohort at 5 years were 34%, 45%, 32%, and 33%, respectively. Outcomes were significantly better in patients with pretransplantation responsive disease (2-year PFS and OS of 50% and 58%, respectively) compared with refractory patients (2-year PFS and OS of 0%). In our multicenter retrospective study, alloHSCT produced durable remissions in a proportion of patients with treatment-sensitive disease before transplantation (5-year PFS of 44%) and should be considered in the treatment of patients with rel/ref PMBCL.
复发或难治性(rel/ref)原发性纵隔大 B 细胞淋巴瘤(PMBCL)的标准治疗方法是挽救治疗,随后进行自体(auto)造血干细胞移植(HSCT)。然而,许多患者患有难治性疾病,无法进行自体 HSCT,而且相当一部分患者在自体 HSCT 后会复发。与弥漫性大 B 细胞淋巴瘤类似,这些患者可能会接受异基因(allo)HSCT 以达到治愈目的,但存在严重发病率和死亡率的风险。鉴于针对 rel/ref PMBCL 的有效免疫治疗方法的出现,了解 alloHSCT 在这些患者中的毒性和疗效非常重要,这些新方法可能是替代方法。因此,我们回顾性研究了 4 个中心的 28 例 rel/ref PMBCL 患者接受 alloHSCT 的多中心队列的结果。大多数患者(79%)对移植前的治疗敏感,86%的患者接受了强度降低的预处理。该队列的 5 年总无进展生存(PFS)、总生存(OS)以及非复发死亡率和复发的累积发生率分别为 34%、45%、32%和 33%。与难治性患者相比,移植前有反应性疾病的患者的结果明显更好(2 年 PFS 和 OS 分别为 50%和 58%)。在我们的多中心回顾性研究中,alloHSCT 在移植前治疗敏感疾病的患者中产生了持久缓解(5 年 PFS 为 44%),并应考虑在治疗 rel/ref PMBCL 患者中使用。