首页> 外文期刊>Journal of Clinical Oncology >Reclassification of 300 primary cutaneous B-Cell lymphomas according to the new WHO-EORTC classification for cutaneous lymphomas: comparison with previous classifications and identification of prognostic markers.
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Reclassification of 300 primary cutaneous B-Cell lymphomas according to the new WHO-EORTC classification for cutaneous lymphomas: comparison with previous classifications and identification of prognostic markers.

机译:根据新的WHO-EORTC皮肤淋巴瘤分类对300例原发性皮肤B细胞淋巴瘤进行重新分类:与以前的分类进行比较并鉴定预后指标。

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PURPOSE: 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. PATIENTS AND METHODS: 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. RESULTS: 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. CONCLUSION: 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.
机译:目的:在新的WHO-欧洲癌症研究和治疗组织(WHO-EORTC)的皮肤淋巴瘤分类中,主要分为三类原发性皮肤B细胞淋巴瘤(CBCL):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)的预后良好,而原发性皮肤大B细胞淋巴瘤腿型(PCLBCL-LT)的预后中等。这项研究旨在评估与以前的分类方案(EORTC 1997; WHO 2001)相比,新分类的临床意义,并在新定义的分类中定义预后因素。患者和方法:在本研究中,对300例先前根据EORTC分类进行分类的CBCL患者的临床资料和组织学切片进行了回顾,并根据WHO和新的WHO-EORTC分类方案进行了重新分类。结果: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年疾病特异性存活率分别为98%,95%和50%。与EORTC和WHO方案相比,5.3%和36.3%的CBCL患者被重新分类为另一种预后类别。 PCFCL的多变量分析显示腿部定位和FOXP1的表达是独立的参数,与预后不良相关。 Bcl-2或MUM-1的表达对这一组患者的生存无明显影响。在PCLBCL-LT中,未发现独立的预后参数。结论:这些结果强调了WHO-EORTC分类的临床意义,但建议在PCFCL组中,应区分腿部淋巴瘤和其他部位淋巴瘤。

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