Jantunen Esa, D'Amore Francesco
Department of Medicine, Kuopio University Hospital, Kuopio, Finland.
Leuk Lymphoma. 2004 Mar;45(3):441-6. doi: 10.1080/10428190310001597955.
Peripheral T-cell lymphomas (PTCL) consist of many subtypes with variable clinical presentation. Long-term prognosis of most subtypes is unfavorable and novel therapeutic approaches are needed. This review attempts to summarize what is known on the feasibility and efficacy of high-dose therapy supported by stem cell transplantation (SCT) in PTCL. In patients with relapsed or refractory PTCL, the outcome of autologous SCT (ASCT) seems to be comparable to that of patients with aggressive B-cell lymphomas. Although excellent treatment results have been encountered with ASCT in patients with anaplastic large cell lymphoma (ALCL), the superiority of this approach over chemotherapy alone needs confirmation in randomized studies. In less favorable subtypes (e.g. alk-negative ALCL, PTCL not otherwise specified, enteropathy-associated T-cell lymphoma, and angioimmunoblastic T-cell lymphoma) high-dose consolidation of the first remission should be studied in prospective trials. Minimal experience is currently available on allogeneic SCT in patients with PTCL. Given the high relapse rate after ASCT in high-risk patients and potential for graft-vs.-lymphoma effect, also this approach should be studied. Due to rarity of PTCL, international collaboration is mandatory in order to study the various aspects of SCT in this patient population.
外周T细胞淋巴瘤(PTCL)由许多具有不同临床表现的亚型组成。大多数亚型的长期预后不佳,需要新的治疗方法。本综述试图总结关于干细胞移植(SCT)支持的高剂量疗法在PTCL中的可行性和疗效的已知情况。在复发或难治性PTCL患者中,自体SCT(ASCT)的结果似乎与侵袭性B细胞淋巴瘤患者相当。虽然间变性大细胞淋巴瘤(ALCL)患者接受ASCT取得了优异的治疗效果,但这种方法相对于单纯化疗的优越性需要在随机研究中得到证实。在预后较差的亚型(如ALK阴性ALCL、未另行指定的PTCL、肠病相关T细胞淋巴瘤和血管免疫母细胞性T细胞淋巴瘤)中,应在前瞻性试验中研究首次缓解后的高剂量巩固治疗。目前关于PTCL患者接受异基因SCT的经验很少。鉴于高危患者ASCT后的高复发率以及移植物抗淋巴瘤效应的可能性,这种方法也应进行研究。由于PTCL罕见,为了研究该患者群体中SCT的各个方面,国际合作是必不可少的。