Senff Nancy J, Zoutman Willem H, Vermeer Maarten H, Assaf Chalid, Berti Emilio, Cerroni Lorenzo, Espinet Blanca, de Misa Cabrera Ricardo Fernandez, Geerts Marie-Louise, Kempf Werner, Mitchell Tracey J, Paulli Marco, Petrella Tony, Pimpinelli Nicola, Santucci Marco, Whittaker Sean J, Willemze Rein, Tensen Cornelis P
Department of Dermatology, Leiden University Medical Center, Leiden, The Netherlands.
J Invest Dermatol. 2009 May;129(5):1149-55. doi: 10.1038/jid.2008.357. Epub 2008 Nov 20.
Primary cutaneous diffuse large B-cell lymphoma, leg type (PCLBCL, LT) is the most aggressive type of primary cutaneous B-cell lymphoma. In a recent study on 12 patients it was found that inactivation of CDKN2A by either deletion of 9p21.3 or promoter hypermethylation is correlated with a worse prognosis. In the present EORTC multicenter study, skin biopsies of 64 PCLBCL, LT patients were analyzed by multiplex ligation-dependent probe amplification to validate these previous results and to fine-map the losses in this region. Although no minimal common region of loss could be identified, most homozygous loss was observed in the CDKN2A gene (43 of 64; 67%) encoding p16 and p14ARF. Promoter hypermethylation of p16 and p14ARF was found in six and zero cases, respectively. Survival was markedly different between patients with versus without aberrations in the CDKN2A gene (5-year disease-specific survival 43 versus 70%; P=0.06). In conclusion, our results confirm that deletion of chromosome 9p21.3 is found in a considerable proportion of PCLBCL, LT patients and that inactivation of the CDKN2A gene is associated with an unfavorable prognosis. In most patients the deletion involves a large area of at least several kilobase pairs instead of a small minimal common region.
原发性皮肤弥漫性大B细胞淋巴瘤,腿部型(PCLBCL,LT)是原发性皮肤B细胞淋巴瘤中侵袭性最强的类型。在最近一项针对12例患者的研究中发现,9p21.3缺失或启动子高甲基化导致的CDKN2A失活与预后较差相关。在当前的欧洲癌症研究与治疗组织(EORTC)多中心研究中,对64例PCLBCL,LT患者的皮肤活检样本进行了多重连接依赖探针扩增分析,以验证先前的结果并精细定位该区域的缺失。尽管未能确定最小的共同缺失区域,但在编码p16和p14ARF的CDKN2A基因中观察到大多数纯合缺失(64例中有43例;67%)。分别在6例和0例中发现了p16和p14ARF的启动子高甲基化。CDKN2A基因有无异常的患者之间生存率存在显著差异(5年疾病特异性生存率分别为43%和70%;P = 0.06)。总之,我们的结果证实,相当一部分PCLBCL,LT患者存在9p21.3染色体缺失,且CDKN2A基因失活与不良预后相关。在大多数患者中,缺失涉及至少几千碱基对的大片区域,而非小的最小共同区域。