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首页> 外文期刊>Leukemia and lymphoma >Negative impact of concurrent overexpression of MYC and BCL2 in patients with advanced diffuse large B-cell lymphoma treated with dose-intensified immunochemotherapy
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Negative impact of concurrent overexpression of MYC and BCL2 in patients with advanced diffuse large B-cell lymphoma treated with dose-intensified immunochemotherapy

机译:剂量增强免疫化学疗法治疗晚期弥漫性大B细胞淋巴瘤的同时MYC和BCL2过表达的负面影响

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摘要

Co-expression of MYC and BCL2 proteins in diffuse large B-cell lymphoma (DLBCL), or 'double-expressor lymphoma' (DEL), results in poor patient prognosis, but the significance of DEL when aggressive treatments are applied remains uncertain. We performed a retrospective analysis of 40 patients with de novo DLBCL, who were categorized as being at high/high-intermediate risk according to the age-adjusted International Prognostic Index. Patients underwent an R-Double CHOP regimen, a dose-intensified immunochemotherapy with or without consolidative high-dose chemotherapy followed by autologous stem cell transplantation. According to immunohistochemical analysis, 10 (25%) patients were categorized as having DEL, showing positivity for MYC (>= 40%) and BCL2 (>= 50%). The 3 year progression-free survival and overall survival of the DEL group were significantly worse compared with those of the non-DEL group (30% vs. 63%, p=0.019 and 40% vs. 82%, p=0.006, respectively). These results suggest that advanced DEL may need discrete treatment strategies.
机译:MYC和BCL2蛋白在弥漫性大B细胞淋巴瘤(DLBCL)或“双表达淋巴瘤”(DEL)中的共表达会导致患者预后不良,但采用积极治疗时DEL的意义尚不确定。我们对40例新生的DLBCL患者进行了回顾性分析,这些患者根据年龄调整后的国际预后指数被归类为高/高中危。患者接受R-Double CHOP方案,在有或没有合并大剂量化疗的情况下进行剂量增强的免疫化学疗法,然后进行自体干细胞移植。根据免疫组化分析,将10名(25%)患者归类为DEL,显示出MYC(> = 40%)和BCL2(> = 50%)阳性。与非DEL组相比,DEL组的3年无进展生存期和总生存期明显更差(分别为30%vs. 63%,p = 0.019和40%vs. 82%,p = 0.006) )。这些结果表明,晚期DEL可能需要离散治疗策略。

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