Hamlin Paul A, Portlock Carol S, Straus David J, Noy Ariela, Singer Andrew, Horwitz Steven M, Oconnor Owen A, Yahalom Joachim, Zelenetz Andrew D, Moskowitz Craig H
Medicine-Lymphoma Service, Memorial Sloan Kettering Cancer Center, New York, NY 10021, USA.
Br J Haematol. 2005 Sep;130(5):691-9. doi: 10.1111/j.1365-2141.2005.05661.x.
Primary mediastinal large B-cell lymphoma (PMLBL) is a distinct clinicopathological entity with unclear prognostic factors and optimal treatment approach. To elucidate an optimal treatment and identify predictive factors, a retrospective analysis of 141 consecutive patients was undertaken. Patients received cyclophosphamide, hydroxydaunomycin, Oncovin, prednisone (CHOP)-like therapy, the non-Hodgkin lymphoma (NHL)-15 regimen or upfront autologous stem cell transplantation (ASCT) on Institutional Review Board approved trials or according to the institutional guidelines. Evaluation included lactate dehydrogenase, International Prognostic Index (IPI) assessment, computed tomography scan and gallium imaging. With a median follow-up of 10.9 years, event-free survival (EFS) and overall survival (OS) was 50% and 66% respectively. EFS/OS for CHOP/CHOP-like, NHL-15 and upfront ASCT was 34/51%, 60/84% and 60/78% respectively. CHOP/CHOP-like regimens had inferior EFS and OS versus NHL-15 or upfront ASCT (P < 0.001). A total of 23% of patients received radiotherapy. Multivariate analysis revealed the following outcome predictors: for EFS, greater than or equal to two extranodal sites and initial therapy received (NHL-15 or upfront ASCT); for OS, only initial therapy with NHL-15. We conclude: (i) dose-dense chemotherapy with NHL-15 may be superior to CHOP for PMLBL; (ii) The impact of consolidative radiotherapy requires randomised controlled trials; (iii) The age-adjusted IPI did not predict survival in this analysis; (iv) high-dose chemotherapy/ASCT should be reserved for upfront anthracycline-based therapy failure or in clinical trials for high-risk patients.
原发性纵隔大B细胞淋巴瘤(PMLBL)是一种独特的临床病理实体,其预后因素和最佳治疗方法尚不清楚。为了阐明最佳治疗方案并确定预测因素,我们对141例连续患者进行了回顾性分析。患者接受了环磷酰胺、羟基柔红霉素、长春新碱、泼尼松(CHOP)样治疗、非霍奇金淋巴瘤(NHL)-15方案或在机构审查委员会批准的试验中或根据机构指南进行的前期自体干细胞移植(ASCT)。评估包括乳酸脱氢酶、国际预后指数(IPI)评估、计算机断层扫描和镓显像。中位随访10.9年,无事件生存期(EFS)和总生存期(OS)分别为50%和66%。CHOP/CHOP样方案、NHL-15方案和前期ASCT的EFS/OS分别为34/51%、60/84%和60/78%。与NHL-15方案或前期ASCT相比,CHOP/CHOP样方案的EFS和OS较差(P<0.001)。共有23%的患者接受了放疗。多变量分析显示了以下预后预测因素:对于EFS,两个或更多结外部位以及接受的初始治疗(NHL-15方案或前期ASCT);对于OS,仅为初始接受NHL-15方案治疗。我们得出结论:(i)对于PMLBL,采用NHL-15方案的剂量密集化疗可能优于CHOP方案;(ii)巩固放疗的影响需要随机对照试验;(iii)在本分析中,年龄校正的IPI不能预测生存;(iv)高剂量化疗/ASCT应保留用于前期基于蒽环类药物治疗失败的患者或用于高危患者的临床试验。