Senff Nancy J, Hoefnagel Juliette J, Jansen Patty M, Vermeer Maarten H, van Baarlen Joop, Blokx Willeke A, Canninga-van Dijk Marijke R, Geerts Marie-Louise, Hebeda Konnie M, Kluin Philip M, Lam King H, Meijer Chris J L M, Willemze Rein
Department of Dermatology, Leiden University Medical Center, Leiden, The Netherlands.
J Clin Oncol. 2007 Apr 20;25(12):1581-7. doi: 10.1200/JCO.2006.09.6396. Epub 2007 Mar 12.
In the new WHO-European Organisation for Research and Treatment of Cancer (WHO-EORTC) classification for cutaneous lymphomas three major groups of primary cutaneous B-cell lymphoma (CBCL) are distinguished: primary cutaneous marginal zone B-cell lymphoma (PCMZL) and primary cutaneous follicle center lymphoma (PCFCL) with a good prognosis, and primary cutaneous large B-cell lymphoma, leg type (PCLBCL-LT), with an intermediate-level prognosis. This study aimed to assess the clinical significance of the new classification compared with previous classification schemes (EORTC 1997; WHO 2001) and to define prognostic factors within the newly defined categories.
In the present study clinical data and histologic sections of 300 patients with CBCL, formerly classified according to the EORTC classification, were reviewed and reclassified according to the WHO and the new WHO-EORTC classification schemes.
After reclassification, the study comprised 71 patients with PCMZL, 171 patients with PCFCL, and 58 patients with PCLBCL-LT, showing 5-year disease-specific survivals of 98%, 95%, and 50%, respectively. When compared with the EORTC and WHO schemes, 5.3% and 36.3% of patients with CBCL were reclassified into another prognostic category. Multivariate analysis of PCFCL revealed localization on the leg and expression of FOXP1 as independent parameters associated with a poor prognosis. Expression of Bcl-2 or MUM-1 had no significant effect on survival in this group. In PCLBCL-LT, no independent prognostic parameters were found.
These results emphasize the clinical significance of the WHO-EORTC classification, but suggest that within the group of PCFCL, distinction should be made between lymphomas presenting on the legs and lymphomas presenting at other sites.
在世界卫生组织-欧洲癌症研究与治疗组织(WHO-EORTC)新的皮肤淋巴瘤分类中,原发性皮肤B细胞淋巴瘤(CBCL)分为三大类:预后良好的原发性皮肤边缘区B细胞淋巴瘤(PCMZL)和原发性皮肤滤泡中心淋巴瘤(PCFCL),以及预后中等的原发性皮肤大B细胞淋巴瘤,腿部型(PCLBCL-LT)。本研究旨在评估新分类与先前分类方案(EORTC 1997;WHO 2001)相比的临床意义,并确定新定义类别中的预后因素。
在本研究中,回顾了300例先前根据EORTC分类的CBCL患者的临床资料和组织切片,并根据WHO和新的WHO-EORTC分类方案重新分类。
重新分类后,该研究包括71例PCMZL患者、171例PCFCL患者和58例PCLBCL-LT患者,其5年疾病特异性生存率分别为98%、95%和50%。与EORTC和WHO方案相比,分别有5.3%和36.3%的CBCL患者被重新分类到另一个预后类别。对PCFCL的多变量分析显示,腿部定位和FOXP1表达是与预后不良相关的独立参数。Bcl-2或MUM-1的表达对该组患者的生存无显著影响。在PCLBCL-LT中,未发现独立的预后参数。
这些结果强调了WHO-EORTC分类的临床意义,但表明在PCFCL组中,应区分腿部出现的淋巴瘤和其他部位出现的淋巴瘤。