Retrospective analysis of intravascular large B-cell lymphoma treated with rituximab-containing chemotherapy as reported by the IVL study group in Japan

Retrospective analysis of intravascular large B-cell lymphoma treated with rituximab-containing chemotherapy as reported by the IVL study group in Japan
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DOI:
10.1200/jco.2007.15.4278
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发表时间:
2008-07-01
影响因子:
45.3
通讯作者:
Kinoshita, Tomohiro
Kinoshita, Tomohiro
中科院分区:
医学1区
文献类型:
--
作者:
Shimada, Kazuyuki;Matsue, Kosei;Kinoshita, Tomohiro

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PurposeTo评估含利妥昔单抗化疗的血管内大B细胞淋巴瘤(IVLBCL)的安全性和有效性。患者和方法我们回顾性分析了106例(59名男性,47名女性)IVLBCL患者,他们在1994年至2007年期间接受利妥昔单抗(R-化疗,n = 49)或不接受利妥昔单抗(化疗,n = 57)。患者的中位年龄为67岁(范围:34 - 84岁)。国际预后指数高-中/高97%的patients.ResultsThe完全缓解率较高的患者在R-化疗组(82%)比化疗组(51%; P = .001)。存活患者的中位随访时间为18个月(范围:1至95个月)。诊断后2年,R-化疗组患者的无进展生存期(PFS)和总生存期(OS)率(PFS,56%; OS,66%)显著高于化疗组患者(PFS,27%,P = 0.001; OS,46%,P = 0.01)。多变量分析显示,利妥昔单抗的使用与PFS(风险比[HR],0.45; 95%CI,0.25 - 0.80; P = 0.006)和OS(HR,0.42; 95%CI,0.21 - 0.85; P = 0.016)有利相关。治疗相关的死亡观察到三名患者(6%)谁接受R-化疗和五名患者(9%)谁接受chemotherapy.ConclusionOur数据表明,利妥昔单抗时代IVLBCL患者的临床结局改善。未来对含利妥昔单抗的化疗进行前瞻性研究是必要的。
PurposeTo evaluate the safety and efficacy of rituximab-containing chemotherapies for intravascular large B-cell lymphoma (IVLBCL).Patients and MethodsWe retrospectively analyzed 106 patients (59 men, 47 women) with IVLBCL who received chemotherapy either with rituximab (R-chemotherapy, n = 49) or without rituximab (chemotherapy, n = 57) between 1994 and 2007 in Japan. The median patient age was 67 years (range, 34 to 84 years). The International Prognostic Index was high-intermediate/high in 97% of patients.ResultsThe complete response rate was higher for patients in the R-chemotherapy group (82%) than for those in the chemotherapy group (51%; P = .001). The median duration of follow-up for surviving patients was 18 months (range, 1 to 95 months). Progression-free survival (PFS) and overall survival (OS) rates at 2 years after diagnosis were significantly higher for patients in the R-chemotherapy group (PFS, 56%; OS, 66%) than for patients in the chemotherapy group (PFS, 27% with P = .001; OS, 46% with P = 0.01). Multivariate analysis revealed that the use of rituximab was favorably associated with PFS (hazard ratio [HR], 0.45; 95% CI, 0.25 to 0.80; P = .006) and OS (HR, 0.42; 95% CI, 0.21 to 0.85; P = .016). Treatment-related death was observed in three patients (6%) who received R-chemotherapy and in five patients (9%) who received chemotherapy.ConclusionOur data suggest improved clinical outcomes for patients with IVLBCL in the rituximab era. Future prospective studies of rituximab-containing chemotherapies are warranted.