Division of Hematology, University of Washington School of Medicine, WA, USA.
Best Pract Res Clin Haematol. 2013 Mar;26(1):89-99. doi: 10.1016/j.beha.2013.04.008. Epub 2013 May 25.
Peripheral T-cell and NK-cell lymphomas (PT/NKCL) are a heterogeneous group of lymphoid neoplasms with poor outcomes. There is no consensus on the best front line therapy or management of relapsed/refractory disease. The use of autologous and allogeneic hematopoietic cell transplantation (HCT) has been studied in both settings to improve outcomes. Multiple retrospective and several prospective trials were reported. While at first sight the outcomes in the relapsed/refractory setting appear similar in B-cell and T-cell lymphomas when treated with high dose therapy (HDT) and autologous HCT, it is becoming obvious that only specific subtypes of PTCL benefit from this approach (i.e. anaplastic large cell lymphoma [ALCL] and angioimmunoblastic lymphoma [AITL] in second CR). In less favorable histologies, HDT seems to provide limited benefit, with the majority of patients experiencing post-transplant relapse. The use of autologous HCT to consolidate first remission has been evaluated in several prospective trials. Again, the best results were observed in ALCL, but the superiority of this approach over chemotherapy alone needs confirmation in randomized trials. In less favorable histologies, high-dose consolidation resulted in low survival rates comparable to those obtained with chemotherapy alone, and without randomized trials it is hard to recommend this strategy to all patients with newly diagnosed PT/NKCL. Allogeneic HCT might provide potent and potentially curative graft-vs-lymphoma effect and overcome chemotherapy resistance. Only a few studies have been reported to date on allogeneic HCT in PT/NKCL. Based on available data, eligible patients benefit significantly from this approach, with 50% or more patients achieving long-term disease control or cure, although at the expense of significant treatment related mortality (TRM). Reduced-intensity conditioning regimens appear to have lower TRM and might extend this approach to older patients. With the recent approval of several novel agents for relapsed/refractory PT/NKCL and their impact on survival of patients after relapse, it is becoming even more difficult to assess the benefit of HCT on overall survival and apply the results of non-randomized studies to clinical practice. Development of effective clinico-pathologic prognostic models might provide the opportunity to better define the role of HCT for patients with various subtypes of PT/NKCL. The first randomized trial comparing upfront autologous and allogeneic HCT was initiated by the German High-Grade Non-Hodgkin Lymphoma Study Group, and the results of this study might help answer some of the controversies for the first time.
外周 T 细胞和自然杀伤 (NK) 细胞淋巴瘤 (PT/NKCL) 是一组异质性的淋巴肿瘤,预后较差。对于一线治疗和复发性/难治性疾病的管理,目前尚无共识。自体和同种异体造血细胞移植 (HCT) 的应用已在这两种情况下进行了研究,以改善预后。多项回顾性和几项前瞻性试验已报告。虽然乍一看,在接受高剂量治疗 (HDT) 和自体 HCT 治疗的复发性/难治性 B 细胞和 T 细胞淋巴瘤中,结果似乎相似,但很明显,只有特定亚型的 PTCL 受益于这种方法(即,间变性大细胞淋巴瘤 [ALCL] 和血管免疫母细胞性 T 细胞淋巴瘤 [AITL] 在第二次完全缓解 [CR] 中)。在预后较差的组织学中,HDT 似乎提供的益处有限,大多数患者在移植后复发。在几项前瞻性试验中评估了自体 HCT 巩固首次缓解的效果。同样,ALCL 观察到的结果最好,但这种方法优于单独化疗的优势仍需在随机试验中得到证实。在预后较差的组织学中,高剂量巩固治疗导致的生存率与单独化疗相似,而且由于没有随机试验,很难向所有新诊断的 PT/NKCL 患者推荐这种策略。同种异体 HCT 可能提供强大且潜在的治愈性移植物抗淋巴瘤效应,并克服化疗耐药性。迄今为止,只有少数关于 PT/NKCL 中同种异体 HCT 的研究报告。基于现有数据,符合条件的患者从这种方法中显著获益,超过 50%的患者实现了长期疾病控制或治愈,尽管代价是显著的治疗相关死亡率 (TRM)。低强度预处理方案似乎具有较低的 TRM,并可能将这种方法扩展到老年患者。随着最近批准了几种用于复发性/难治性 PT/NKCL 的新型药物及其对复发后患者生存的影响,评估 HCT 对总生存的获益并将非随机研究的结果应用于临床实践变得更加困难。有效的临床病理预后模型的开发可能为更好地定义各种亚型的 PT/NKCL 患者的 HCT 作用提供机会。德国高级非霍奇金淋巴瘤研究组发起了一项比较一线自体和同种异体 HCT 的随机试验,该研究的结果可能首次帮助解答一些争议。