Foran J M, Rohatiner A Z, Coiffier B, Barbui T, Johnson S A, Hiddemann W, Radford J A, Norton A J, Tollerfield S M, Wilson M P, Lister T A
Department of Histopathology, St. Bartholomew's Hospital, London, England.
J Clin Oncol. 1999 Feb;17(2):546-53. doi: 10.1200/JCO.1999.17.2.546.
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.
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).
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.
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.
磷酸氟达拉滨(F-AMP)在滤泡性淋巴瘤和B细胞慢性淋巴细胞白血病中具有显著活性,已显示出较高的完全缓解(CR)率。淋巴浆细胞样(LPC)淋巴瘤、华氏巨球蛋白血症(WM)和套细胞淋巴瘤(MCL)也表现为晚期疾病,采用基于烷化剂的标准化疗无法治愈。开展了一项II期试验以确定F-AMP对新诊断出这些疾病的患者的活性。
1992年至1996年期间,78例年龄在18至75岁的患者接受静脉注射F-AMP(25mg/m²/天,共5天,每4周一次)直至出现最大反应,再加上两个巩固周期。主要终点为缓解率;次要终点包括疾病进展时间(TTP)、缓解持续时间和总生存期(OS)。
71例可评估患者中有44例(62%)对F-AMP有反应(LPC淋巴瘤,63%;WM,79%;MCL,41%);CR率为15%。中位随访1.5年时,44例有反应的患者中有19例出现淋巴瘤进展;中位缓解持续时间为2.5年。中位生存期尚未达到。不同组织学类型的患者在缓解持续时间或OS方面无显著差异;MCL患者的TTP较短(P = 0.015)。骨髓抑制相对常见,治疗相关死亡率(TRM)为5%,主要与全血细胞减少和感染有关。
单药磷酸氟达拉滨对既往未治疗的LPC淋巴瘤和WM有活性,对MCL只有中度活性。然而,CR率较低,TRM相对较高。其在联合化疗中的作用仍有待证实。