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R-CHOP或CHOP方案治疗中国患者弥漫性大B细胞淋巴瘤生发中心型和非生发中心型的疗效

Outcome of R-CHOP or CHOP regimen for germinal center and nongerminal center subtypes of diffuse large B-cell lymphoma of Chinese patients.

作者信息

Huang Ying, Ye Sheng, Cao Yabing, Li Zhiming, Huang Jiajia, Huang He, Cai Muyan, Luo Rongzhen, Lin Tongyu

机构信息

State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, 651 Dongfeng Road East, Guangzhou 510060, China.

出版信息

ScientificWorldJournal. 2012;2012:897178. doi: 10.1100/2012/897178. Epub 2012 Nov 4.

Abstract

Diffuse large B-cell lymphoma (DLBCL) can be molecularly subtyped as either germinal center B-cell (GCB) or non-GCB. The role of rituximab(R) in these two groups remains unclear. We studied 204 patients with de novo DLBCL (107 treated with first-line CHOP; 97 treated with first-line R-CHOP), patients being stratified into GCB and non-GCB on the basis of BCL-6, CD10, and MUM1 protein expression. The relationships between clinical characteristics, survival data, and immunophenotype (IHC) were studied. The 5-year overall survival (OS) in the CHOP and R-CHOP groups was 50.4% and 66.6% (P = 0.031), respectively. GCB patients had a better 5-year OS than non-GCB patients whether treated with CHOP or not (65.0% versus 40.9%; P = 0.011). In contrast, there is no difference in the 5-year OS for the GCB and non-GCB with R-CHOP (76.5% versus 61.3%; P = 0.141). In non-GCB subtype, additional rituximab improved survival better than CHOP (61.3% versus 40.9%; P = 0.0303). These results indicated that addition of rituximab to standard chemotherapy eliminates the prognostic value of IHC-defined GCB and non-GCB phenotypes in DLBCL by improving the prognostic value of non-GCB subtype of DLBCL.

摘要

弥漫性大B细胞淋巴瘤(DLBCL)在分子水平上可分为生发中心B细胞(GCB)型或非GCB型。利妥昔单抗(R)在这两组中的作用仍不明确。我们研究了204例初治DLBCL患者(107例接受一线CHOP治疗;97例接受一线R-CHOP治疗),根据BCL-6、CD10和MUM1蛋白表达将患者分为GCB型和非GCB型。研究了临床特征、生存数据和免疫表型(免疫组化)之间的关系。CHOP组和R-CHOP组的5年总生存率(OS)分别为50.4%和66.6%(P = 0.031)。无论是否接受CHOP治疗,GCB型患者的5年OS均优于非GCB型患者(65.0%对40.9%;P = 0.011)。相比之下,接受R-CHOP治疗的GCB型和非GCB型患者的5年OS无差异(76.5%对61.3%;P = 0.141)。在非GCB亚型中,加用利妥昔单抗比CHOP更能提高生存率(61.3%对40.9%;P = 0.0303)。这些结果表明,在标准化疗中添加利妥昔单抗可通过提高DLBCL非GCB亚型的预后价值,消除免疫组化定义GCB和非GCB表型在DLBCL中的预后价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/3504400/9d32147a7eae/TSWJ2012-897178.001.jpg

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