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

机译:弥漫性大B细胞淋巴瘤患者CyclOBEAP加利妥昔单抗的多中心II期研究。

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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 IPI, 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 >or=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.
机译:已发现R-CHOP方案可改善弥漫性大B细胞淋巴瘤(DLBCL)的预后。但是,它在高危组中不能提供令人满意的治疗结果。我们先前曾向患有DLBCL的患者使用CyclOBEAP方案,并报告了其安全性和有效性。 R-CyclOBEAP方案的给药期为12周,每2周给予rituximab 375 mg / m(2)。有101名合格患者。 96例患者(95%)达到CR。 5年总生存(OS)率为85%,无进展生存(PFS)率为76%。根据IPI对患者进行划分时,各风险组之间的5年OS和PFS率无显着差异。生发中心B细胞组的5年PFS为80%,非GCB组的5年PFS为74%(NS)。单因素分析显示,B症状,结外病灶>或= 2和sIL-2R的存在是显着的不良预后因素。 91例患者观察到4级中性粒细胞减少,9例患者观察到血小板减少。在CyclOBEAP治疗中加入利妥昔单抗可以增强CyclOBEAP治疗DLBCL的效果。

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