首页> 外文期刊>Journal of Clinical Oncology >Multicenter phase II study of fludarabine phosphate for patients with newly diagnosed lymphoplasmacytoid lymphoma, Waldenstrom's macroglobulinemia, and mantle-cell lymphoma.
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Multicenter phase II study of fludarabine phosphate for patients with newly diagnosed lymphoplasmacytoid lymphoma, Waldenstrom's macroglobulinemia, and mantle-cell lymphoma.

机译:氟达拉滨磷酸酯在新诊断的淋巴浆细胞样淋巴瘤,Waldenstrom巨球蛋白血症和套细胞淋巴瘤患者中的多中心II期研究。

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PURPOSE: Fludarabine phosphate (F-AMP) has significant activity in follicular lymphoma and in B-cell chronic lymphatic leukemia, where it has demonstrated high complete response (CR) rates. Lymphoplasmacytoid (LPC) lymphoma, Waldenstrom's macroglobulinemia (WM), and mantle-cell lymphoma (MCL) also present with advanced-stage disease and are incurable with standard alkylator-based chemotherapy. A phase II trial was undertaken to determine the activity of F-AMP in patients newly diagnosed with these diseases. PATIENTS AND METHODS: Between 1992 and 1996, 78 patients (aged 18 to 75 years) received intravenous F-AMP (25 mg/m2/d for 5 days, every 4 weeks) until maximum response, plus two further cycles as consolidation. The primary end point was response rate; secondary end points included time to progression (TTP), duration of response, and overall survival (OS). RESULTS: Forty-four (62%) of 71 assessable patients had a response to F-AMP (LPC lymphoma, 63%; WM, 79%; MCL, 41%); the CR rate was 15%. At a median follow-up of 1.5 years, 19 of 44 responding patients have had progression of lymphoma; the median duration of response was 2.5 years. The median survival has not yet been reached. There was no significant difference in the duration of response or OS between patients with different histologies; TTP was shorter in patients with MCL (P = .015). Myelosuppression was relatively common, and the treatment-related mortality (TRM) was 5%, mostly associated with pancytopenia and infection. CONCLUSION: Single-agent fludarabine phosphate is active in previously untreated LPC lymphoma and WM, with only moderate activity in MCL. However, the CR rate is low, and the TRM is relatively high. Its role in combination chemotherapy remains to be demonstrated.
机译:目的:磷酸氟达拉滨(F-AMP)在滤泡性淋巴瘤和B细胞慢性淋巴白血病中均具有显着活性,并在其中表现出较高的完全缓解(CR)率。淋巴浆细胞样(LPC)淋巴瘤,Waldenstrom巨球蛋白血症(WM)和套细胞淋巴瘤(MCL)也存在晚期疾病,并且使用基于烷基化器的标准化疗无法治愈。进行了一项II期试验,以确定新诊断为这些疾病的患者中F-AMP的活性。患者与方法:在1992年至1996年之间,有78位患者(年龄在18至75岁之间)接受了静脉F-AMP(25 mg / m2 / d,连续5天,每4周一次),直到达到最大缓解为止,另外还进行了两次巩固治疗。主要终点是反应率。次要终点包括进展时间(TTP),反应持续时间和总生存期(OS)。结果:71名可评估患者中有44名(62%)对F-AMP有反应(LPC淋巴瘤为63%; WM为79%; MCL为41%); CR率为15%。在1.5年的中位随访中,有44例反应者中有19例进展为淋巴瘤;中位反应时间为2.5年。中位生存期尚未达到。不同组织学的患者反应或OS持续时间无显着差异。 MCL患者的TTP较短(P = .015)。骨髓抑制相对常见,与治疗有关的死亡率(TRM)为5%,主要与全血细胞减少和感染有关。结论:单药氟达拉滨磷酸酯在先前未治疗的LPC淋巴瘤和WM中具有活性,在MCL中仅具有中等活性。但是,CR率较低,TRM较高。它在联合化疗中的作用仍有待证明。

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