Shimada Kazuyuki, Matsue Kosei, Yamamoto Kazuhito, Murase Takuhei, Ichikawa Naoaki, Okamoto Masataka, Niitsu Nozomi, Kosugi Hiroshi, Tsukamoto Norifumi, Miwa Hiroshi, Asaoku Hideki, Kikuchi Ako, Matsumoto Morio, Saburi Yoshio, Masaki Yasufumi, Yamaguchi Motoko, Nakamura Shigeo, Naoe Tomoki, Kinoshita Tomohiro
Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550 Japan.
J Clin Oncol. 2008 Jul 1;26(19):3189-95. doi: 10.1200/JCO.2007.15.4278. Epub 2008 May 27.
To evaluate the safety and efficacy of rituximab-containing chemotherapies for intravascular large B-cell lymphoma (IVLBCL).
We 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.
The 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.
Our data suggest improved clinical outcomes for patients with IVLBCL in the rituximab era. Future prospective studies of rituximab-containing chemotherapies are warranted.
评估含利妥昔单抗的化疗方案治疗血管内大B细胞淋巴瘤(IVLBCL)的安全性和疗效。
我们回顾性分析了1994年至2007年期间在日本接受化疗的106例IVLBCL患者(59例男性,47例女性),其中49例接受含利妥昔单抗的化疗(R-化疗组),57例未接受利妥昔单抗化疗(化疗组)。患者中位年龄为67岁(范围34至84岁)。97%的患者国际预后指数为高中/高。
R-化疗组患者的完全缓解率(82%)高于化疗组(51%;P = 0.001)。存活患者的中位随访时间为18个月(范围1至95个月)。R-化疗组患者诊断后2年的无进展生存率(PFS)和总生存率(OS)显著高于化疗组(PFS,56%;OS,66%),化疗组PFS为27%(P = 0.001),OS为46%(P = 0.01)。多因素分析显示,使用利妥昔单抗与PFS(风险比[HR],0.45;95%可信区间[CI],0.25至0.80;P = 0.006)和OS(HR,0.42;95%CI,0.21至0.85;P = 0.016)呈正相关。接受R-化疗的3例患者(6%)和接受化疗的5例患者(9%)出现治疗相关死亡。
我们的数据表明,在利妥昔单抗时代,IVLBCL患者的临床结局有所改善。有必要对含利妥昔单抗的化疗方案进行未来的前瞻性研究。