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每周与每两周一次硼替佐米联合利妥昔单抗治疗复发性滤泡性淋巴瘤、套细胞淋巴瘤和华氏巨球蛋白血症患者。

Weekly versus twice weekly bortezomib given in conjunction with rituximab, in patients with recurrent follicular lymphoma, mantle cell lymphoma and Waldenström macroglobulinaemia.

机构信息

CR-UK Medical Oncology Unit, St Bartholomew's Hospital, London, UK.

出版信息

Br J Haematol. 2010 Nov;151(4):346-53. doi: 10.1111/j.1365-2141.2010.08340.x. Epub 2010 Sep 29.

Abstract

The combination of bortezomib and rituximab was evaluated in patients with mantle cell lymphoma (MCL), follicular lymphoma (FL) and Waldenström macroglobulinaemia (WM), in a Phase I and later, a randomized Phase II study. In the randomized study, 42 patients with recurrent/refractory disease received either: bortezomib 1·3 mg/m(2) on days 1, 4, 8 and 11 of a 3-week cycle with rituximab 375 mg/m(2) on day 1 (21 patients) or: bortezomib 1·6 mg/m(2) and rituximab on days 1, 8, 15 and 22 of a 5-week cycle (with rituximab being given only in cycles 1 and 4).Twenty-eight patients were withdrawn (toxicity 16, progression 7, and 'patient choice' 5). The main toxicities were neurological, gastro-intestinal and haematological. The overall response rate was 28/42(67%) and by histology: MCL 11/19, FL 8/15, and WM 9/10. Ten of 28 responding patients remained progression-free at 1-3·5 years. Toxicity and efficacy were equivalent between the two groups. The combination has significant toxicity but is effective, particularly in patients with WM.

摘要

硼替佐米和利妥昔单抗联合治疗套细胞淋巴瘤(MCL)、滤泡性淋巴瘤(FL)和华氏巨球蛋白血症(WM)患者的 1 期和随后的随机 2 期研究。在这项随机研究中,42 例复发性/难治性疾病患者接受以下治疗:硼替佐米 1.3 mg/m2,在每 3 周周期的第 1、4、8 和 11 天,利妥昔单抗 375 mg/m2,在第 1 天(21 例);或硼替佐米 1.6 mg/m2 和利妥昔单抗,在每 5 周周期的第 1、8、15 和 22 天(仅在周期 1 和 4 给予利妥昔单抗)。28 例患者退出(毒性 16 例,进展 7 例,“患者选择”5 例)。主要毒性为神经、胃肠和血液学毒性。总缓解率为 42/42(67%),按组织学:MCL 11/19,FL 8/15,WM 9/10。28 例缓解患者中有 10 例在 1-3.5 年内无疾病进展。两组间毒性和疗效相当。该联合方案具有显著的毒性,但有效,特别是在 WM 患者中。

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