Service d'Onco-Hématologie, Hôpital de l'Archet, Nice, France.
Curr Opin Oncol. 2011 Mar;23(2):209-13. doi: 10.1097/CCO.0b013e328342b8ad.
Addition of rituximab to conventional chemotherapies was shown to improve outcome in phase 3 trials of patients with diffuse large B-cell lymphoma (DLBCL). As the challenge in the rituximab era is to increase treatment efficacy, the present review attempts to assess the results of high-dose therapy and autologous stem cell transplantation (ASCT) as front-line treatment for poor-prognosis DLBCL patients.
French and Italian groups demonstrated in several phase 2 series that high-dose front-line treatment with rituximab plus ASCT gave better results than without rituximab. In relapse, the CORAL study, a worldwide collaborative effort, showed that assessment of the latest results for ASCT should also take account of other prognostic factors, including advanced stage, chemo/rituximab refractory disease and a short interval between remission and relapse. This underscores the need for innovative therapeutic strategies such as radiolabelled conditioning regimens and maintenance after ASCT. Allogeneic transplantation, which generates a graft-versus-lymphoma effect that reduces the likelihood of relapse, may also be beneficial for high-risk patients.
In this setting, new approaches based on improved understanding of the biology of the disease will play a key role.
利妥昔单抗联合常规化疗在弥漫性大 B 细胞淋巴瘤(DLBCL)的 3 期临床试验中显示可改善结局。由于在利妥昔单抗时代的挑战是提高治疗效果,本综述尝试评估大剂量治疗和自体干细胞移植(ASCT)作为不良预后 DLBCL 患者一线治疗的结果。
法国和意大利的几个 2 期系列研究表明,利妥昔单抗联合 ASCT 进行高剂量一线治疗的效果优于没有利妥昔单抗的治疗。在复发时,一项全球合作的 CORAL 研究表明,评估 ASCT 的最新结果还应考虑其他预后因素,包括晚期、化疗/利妥昔单抗难治性疾病以及缓解与复发之间的短间隔。这强调了需要采用创新的治疗策略,例如放射性标记的预处理方案和 ASCT 后的维持治疗。异基因移植可产生移植物抗淋巴瘤效应,降低复发的可能性,对高危患者也可能有益。
在这种情况下,基于对疾病生物学的深入理解而提出的新方法将发挥关键作用。