Li Linyu, Zhang Xuhan, Zhang Tingting, Song Zheng, Hu Ge, Li Wei, Li Lanfang, Qiu Lihua, Qian Zhengzi, Zhou Shiyong, Liu Xianming, Feng Lixia, Pan Yi, Zhai Qiongli, Meng Bin, Ren Xiubao, Fu Kai, Wang Ping, Wang Xianhuo, Zhang Huilai
Department of Lymphoma, Sino-US Center for Lymphoma and Leukemia Research, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center of Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China.
Department of Pathology, Sino-US Center for Lymphoma and Leukemia Research, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center of Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China.
Clin Lymphoma Myeloma Leuk. 2018 Oct;18(10):e381-e389. doi: 10.1016/j.clml.2018.06.010. Epub 2018 Jun 19.
Double-expression lymphoma (DEL) is a rare subgroup of diffuse large B-cell lymphoma (DLBCL), which has coexpression of MYC and BCL-2. Coexpression of MYC and BCL-2 is considered a prognostic marker portending poor outcomes. However, the prognostic effect of BCL-2 and BCL-6 expression in DLBCL remains controversial.
Immunohistochemical staining was performed to detect MYC, BCL-2 and BCL-6 expression in 212 patients with newly diagnosed DLBCL and assess the prognostic effects of BCL-2 and BCL-6 expression. The DLBCL patients were treated with R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine [Oncovin], prednisone)-like regimens.
Retrospective analysis revealed that BCL-2 and BCL-2/MYC were prognostic factors indicative of poor outcomes. Patients with BCL-2 and/or MYC expression had a poorer prognosis than that of patients with BCL-2 and/or MYC expression. Patients with BCL-2/MYC expression showed a trend toward poorer survival than those with BCL-2/MYC expression, suggesting that BCL-2 plays a more important role than MYC. Also, patients with BCL-6/MYC expression had poorer progression-free survival than those with BCL-6/MYC expression. In addition, patients with BCL-2/MYC/BCL-6 expression had the worst prognosis, suggesting that BCL-6 is a prognostic factor for poor outcomes for MYC DLBCL patients. Altogether, our findings have shown that BCL-2 is an independent prognostic factor and possibly plays a more important role than MYC in MYC DLBCL patients. Furthermore, we found that BCL-6 expression could also be a prognostic factor portending poor outcomes for MYC DLBCL patients.
双表达淋巴瘤(DEL)是弥漫性大B细胞淋巴瘤(DLBCL)的一个罕见亚组,其具有MYC和BCL-2的共表达。MYC和BCL-2的共表达被认为是预后不良的一个预后标志物。然而,BCL-2和BCL-6表达在DLBCL中的预后作用仍存在争议。
对212例新诊断的DLBCL患者进行免疫组织化学染色,以检测MYC、BCL-2和BCL-6的表达,并评估BCL-2和BCL-6表达的预后作用。DLBCL患者接受类似R-CHOP(利妥昔单抗加环磷酰胺、多柔比星、长春新碱[安可平]、泼尼松)方案的治疗。
回顾性分析显示,BCL-2和BCL-2/MYC是提示预后不良的预后因素。有BCL-2和/或MYC表达的患者比没有BCL-2和/或MYC表达的患者预后更差。有BCL-2/MYC表达的患者比没有BCL-2/MYC表达的患者有生存较差的趋势,表明BCL-2比MYC发挥更重要的作用。此外,有BCL-6/MYC表达的患者比没有BCL-6/MYC表达的患者无进展生存期更差。另外,有BCL-2/MYC/BCL-6表达的患者预后最差,表明BCL-6是MYC DLBCL患者预后不良的一个预后因素。总之,我们的研究结果表明,BCL-2是一个独立的预后因素,并且在MYC DLBCL患者中可能比MYC发挥更重要的作用。此外,我们发现BCL-6表达也可能是MYC DLBCL患者预后不良的一个预后因素。