Miyazaki Kana
Department of Hematology and Oncology, Mie University Graduate School of Medicine.
J Clin Exp Hematop. 2016;56(2):79-88. doi: 10.3960/jslrt.56.79.
Diffuse large B-cell lymphoma (DLBCL) comprises a heterogeneous group with pathophysiological, genetic and clinical features. Many patients can be cured with R-CHOP therapy, which is the current standard regimen. Despite recent progress in improving patient survival, the 40% survival of DLBCL patients remains poor. Therefore, the most important issue for patients with DLBCL remains the development of a new front-line therapy. Several studies have reported that intensified chemotherapy with dose-adjusted EPOCH-R or R-ACVBP was superior to R-CHOP. Gene expression profiling has identified two distinct forms of DLBCL: activated B cell-like (ABC) and germinal center B-cell-like (GCB) types. ABC DLBCL exhibits a worse prognosis than GCB DLBCL by molecular diagnosis after R-CHOP therapy. Next-generation sequencing has identified unique oncogenic mechanisms and genetic complexity, which has provided rational therapeutic targets. There are also a number of biomarkers, including CD5, and prognostic factors. Efforts to distinguish many biomarkers will be crucial for individualized treatment in the future.
弥漫性大B细胞淋巴瘤(DLBCL)是一组具有病理生理、遗传和临床特征的异质性疾病。许多患者可通过R-CHOP疗法治愈,这是目前的标准治疗方案。尽管最近在提高患者生存率方面取得了进展,但DLBCL患者40%的生存率仍然很低。因此,DLBCL患者最重要的问题仍然是开发新的一线治疗方法。几项研究报告称,剂量调整的EPOCH-R或R-ACVBP强化化疗优于R-CHOP。基因表达谱分析确定了DLBCL的两种不同形式:活化B细胞样(ABC)和生发中心B细胞样(GCB)类型。经R-CHOP治疗后,通过分子诊断发现ABC DLBCL的预后比GCB DLBCL更差。下一代测序确定了独特的致癌机制和遗传复杂性,这提供了合理的治疗靶点。还有许多生物标志物,包括CD5,以及预后因素。区分众多生物标志物的努力对未来的个体化治疗至关重要。