Gang Anne O, Pedersen Mette Ø, Knudsen Helle, Lauritzen Anne F, Pedersen Michael, Nielsen Signe L, Brown Peter, Høgdall Estrid, Klausen Tobias W, Nørgaard Peter
Department of Hematology.
Leuk Lymphoma. 2015 Jul;56(7):2039-46. doi: 10.3109/10428194.2014.982645. Epub 2015 Jan 21.
Addition of etoposide to the R-CHOP chemotherapy regimen with cyclophosphamide, doxorubicin, vincristine, prednisone and rituximab (R-CHOEP) has resulted in improved survival in young patients with high-risk diffuse large B-cell lymphoma (DLBCL). It is not known whether biological factors can predict this effect. In this study, 245 patients representing all young patients with high-risk DLBCL treated with R-CHOP or R-CHOEP in 2004-2012 in Denmark were extracted from the Danish lymphoma database. Patients were stratified according to cell of origin (COO) into germinal-center B-cell-like (GCB) or non-GCB by Hans' algorithm. Only in patients with the GCB phenotype was treatment with R-CHOEP associated with improved progression-free survival (PFS) and overall survival (OS) compared with R-CHOP. Patients with GCB phenotype treated with R-CHOEP also had superior OS compared with patients with non-GCB phenotype treated with R-CHOEP. This was not seen in R-CHOP treated patients. This could suggest that R-CHOEP should be restricted to patients with GCB phenotype.
在环磷酰胺、阿霉素、长春新碱、泼尼松和利妥昔单抗组成的R-CHOP化疗方案(R-CHOEP)中加入依托泊苷,可提高高危弥漫性大B细胞淋巴瘤(DLBCL)年轻患者的生存率。目前尚不清楚生物学因素是否能预测这种效果。在本研究中,从丹麦淋巴瘤数据库中提取了2004年至2012年在丹麦接受R-CHOP或R-CHOEP治疗的所有高危DLBCL年轻患者,共245例。根据起源细胞(COO),采用汉斯算法将患者分为生发中心B细胞样(GCB)或非GCB。仅在GCB表型的患者中,与R-CHOP相比,R-CHOEP治疗可改善无进展生存期(PFS)和总生存期(OS)。与接受R-CHOEP治疗的非GCB表型患者相比,接受R-CHOEP治疗的GCB表型患者的OS也更优。在接受R-CHOP治疗的患者中未观察到这种情况。这可能表明R-CHOEP应仅限于GCB表型的患者。