Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu.
Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu.
Ann Oncol. 2011 Jul;22(7):1601-1607. doi: 10.1093/annonc/mdq627. Epub 2011 Jan 3.
CD5-positive (CD5+) diffuse large B-cell lymphoma (DLBCL) shows poor prognosis and frequent central nervous system (CNS) relapses under anthracycline-containing chemotherapy. The aim of this study was to determine the prognosis and CNS relapse incidence of CD5+ DLBCL in the rituximab era.
We analyzed 337 patients with CD5+ DLBCL who received chemotherapy with (R-chemotherapy group; n = 184) or without (chemotherapy group; n = 153) rituximab.
No significant difference was found in clinical background comparisons between the two groups. In the R-chemotherapy group, 60% of the patients were older than 65 years at diagnosis. Both the complete response rate and overall survival (OS) were significantly better in the R-chemotherapy group (P = 0.0003 and P = 0.002, respectively). Multivariate analysis confirmed that chemotherapy without rituximab was associated with unfavorable OS. However, the probability of CNS relapse did not differ between the two groups (P = 0.89). The CNS relapse was strongly associated with short OS (P < 0.0001). In the R-chemotherapy group, 83% of patients who experienced CNS relapse had parenchymal disease.
Our results indicate that rituximab improves the OS of patients with CD5+ DLBCL but does not decrease the CNS relapse rate. More effective treatments with CNS prophylaxis are needed for CD5+ DLBCL patients.
在含蒽环类药物的化疗中,CD5 阳性(CD5+)弥漫性大 B 细胞淋巴瘤(DLBCL)预后较差,中枢神经系统(CNS)复发频繁。本研究旨在确定利妥昔单抗时代 CD5+DLBCL 的预后和 CNS 复发率。
我们分析了 337 例接受化疗的 CD5+DLBCL 患者,其中接受利妥昔单抗化疗(R-化疗组;n=184)或未接受利妥昔单抗化疗(化疗组;n=153)。
两组患者的临床背景比较无显著差异。在 R-化疗组中,60%的患者在诊断时年龄大于 65 岁。R-化疗组的完全缓解率和总生存率(OS)均显著提高(P=0.0003 和 P=0.002)。多因素分析证实,未使用利妥昔单抗的化疗与不良 OS 相关。然而,两组 CNS 复发的概率无差异(P=0.89)。CNS 复发与较短的 OS 密切相关(P<0.0001)。在 R-化疗组中,83%经历 CNS 复发的患者有实质疾病。
我们的结果表明,利妥昔单抗改善了 CD5+DLBCL 患者的 OS,但并未降低 CNS 复发率。对于 CD5+DLBCL 患者,需要更有效的 CNS 预防治疗。