Department of Oncology and Hematology, University of Modena and Reggio Emilia, Modena.
Department of Oncology and Hematology, University of Modena and Reggio Emilia, Modena.
Ann Oncol. 2010 Jul;21(7):1486-1491. doi: 10.1093/annonc/mdp531. Epub 2009 Nov 17.
Improved treatment have modified survival outcome in patients with diffuse large B-cell lymphoma (DLBCL) and altered the importance of previously recognized prognostic markers.
To evaluate International Prognostic Index (IPI) score before and after rituximab introduction and to validate the absolute lymphocyte count (ALC)/revised International Prognostic Index (R-IPI) model, we carried out a retrospective analysis on a total of 831 patients with DLBCL.
Our results show that IPI lost its discriminating power with the introduction of rituximab. The analysis of our second set allowed us to validate the ALC/R-IPI model. The R-IPI and ALC/R-IPI could still be used for designing clinical trials, but both have difficulty recognizing a high percentage of poor prognosis patients, though it remains an important goal of a good prognostic model considering the modest impact of salvage treatments on survival.
A new model on the basis of significant variables in the rituximab era and built on a large database of patients treated with rituximab is urgently needed. As prognostic models are changing with the efficacy and mechanisms of action of treatment utilized, looking for a new prognostic score is a never-ending story in which researchers are trying to hit a continuously moving target.
改良治疗方案改变了弥漫性大 B 细胞淋巴瘤(DLBCL)患者的生存结局,并改变了先前公认的预后标志物的重要性。
为了评估利妥昔单抗引入前后国际预后指数(IPI)评分的变化,并验证绝对淋巴细胞计数(ALC)/修订后的国际预后指数(R-IPI)模型,我们对 831 例 DLBCL 患者进行了回顾性分析。
我们的结果表明,随着利妥昔单抗的引入,IPI 丧失了区分能力。我们的第二组分析允许我们验证 ALC/R-IPI 模型。R-IPI 和 ALC/R-IPI 仍然可用于设计临床试验,但两者都难以识别出高比例的预后不良患者,尽管考虑到挽救治疗对生存的影响有限,这仍然是一个良好预后模型的重要目标。
在利妥昔单抗时代基于重要变量的基础上建立的新模型,并在接受利妥昔单抗治疗的大量患者数据库上构建,这是一个迫切需要的新模型。由于预后模型随着治疗效果和作用机制的变化而变化,因此寻找新的预后评分是一个永无止境的故事,研究人员正在努力击中不断移动的目标。