Multicentre phase II study of CyclOBEAP plus rituximab in patients with diffuse large B-cell lymphoma

被引:10
作者
Niitsu, Nozomi [1 ]
Kohri, Mika [1 ]
Hagiwara, Yuki [1 ]
Tanae, Ken [1 ]
Takahashi, Naoki [1 ]
Bessho, Masami [1 ]
Okamoto, Masataka
机构
[1] Saitama Med Univ, Dept Hematol, Ctr Comprehens Canc, Int Med Ctr, Hidaka, Saitama 3501298, Japan
关键词
diffuse large B-cell lymphoma; CyclOBEAP; rituximab; soluble interleukin-2 receptor; RANDOMIZED CONTROLLED-TRIAL; HIGH-DOSE CHEMOTHERAPY; POOR-PROGNOSIS; GERMINAL CENTER; ELDERLY-PATIENTS; CHOP; TRANSPLANTATION; ETOPOSIDE; SURVIVAL; REGIMEN;
D O I
10.1002/hon.940
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The R-CHOP regimen has been found to improve the outcome of diffuse large B-cell lymphoma (DLBCL). However, it does not provide a satisfactory treatment outcome in the high-risk group. We previously administered the CyclOBEAP regimen to patients with DLBCL, and reported its safety and efficacy. The R-CyclOBEAP regimen was administered over a total period of 12 weeks, and rituximab 375 mg/m(2) was given every 2 weeks. There were 101 eligible patients. CR was achieved in 96 patients (95%). The 5-year overall survival (OS) rate was 85% and progression-free survival (PFS) rate was 76%. When the patients were divided according to the IN, the 5-year OS and PFS rates did not significantly differ among the risk groups. The 5-year PFS of the germinal centre B-cell group was 80% and that of the non-GCB group was 74% (NS). Univariate analysis showed that the presence of B symptoms, extranodal lesions >= 2, and sIL-2R were significant poor prognostic factors. Grade 4 neutropenia was observed in 91 patients and thrombocytopenia in 9 patients. The addition of rituximab to CyclOBEAP therapy may enhance the effect of CyclOBEAP therapy for DLBCL. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:68 / 74
页数:7
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