首页> 外文期刊>Haematologica >Fludarabine + prednisone +/- alpha-interferon followed or not by alpha-interferon maintenance therapy for previously untreated patients with chronic lymphocytic leukemia: long term results of a randomized study | Haematologica
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Fludarabine + prednisone +/- alpha-interferon followed or not by alpha-interferon maintenance therapy for previously untreated patients with chronic lymphocytic leukemia: long term results of a randomized study | Haematologica

机译:氟达拉滨+泼尼松+/-α-干扰素联合或不联合α-干扰素维持治疗,对先前未经治疗的慢性淋巴细胞性白血病患者:一项随机研究的长期结果血液学

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BACKGROUND AND OBJECTIVES: Fludarabine is an effective therapy for patients with chronic lymphocytic leukemia (CLL) and interferon-alpha (IFN-alpha) has been reported to have anti-leukemic activity in CLL patients. A randomized study was designed to evaluate whether the addition of IFN-alpha to a first-line treatment with fludarabine and prednisone could increase the response rate in patients with advanced CLL and whether IFN-alpha given as maintenance therapy could improve the duration of response. DESIGN AND METHODS: One hundred and thirty-three patients were randomized to receive fludarabine (25 mg/m2/i.v., days 9-13) and prednisone (20 mg/m2, days 1, 3, 5, 7 and 14 and 40 mg/m2, days 9-13) (arm A: 66 patients) or in addition to the same schedule, IFN-alpha (2 MUI/sc, days 1, 3, 5, 7, 9, 11, 13 and 15) (arm B: 67 patients). Seventy-eight patients responsive to therapy entered the post-remission phase of the study in which 41 patients were randomized to receive IFN-alpha (3 MUI three times a week) and 37 to clinical observation. RESULTS: A similar response rate (complete responses + partial responses) was observed in the 2 arms: 86% for arm A and 84% for arm B (p = 0.4). A longer response duration was observed in patients who achieved a complete response (p = 0.001) and in patients who received maintenance therapy with IFN-alpha (p < 0.05). However, the quality of response was the only significant and independent factor influencing response duration (p < 0.01). No benefits in terms of infection-related mortality and morbidity could be ascribed to IFN-alpha administration. INTERPRETATION AND CONCLUSIONS: In previously untreated CLL patients with advanced disease a high response rate is obtained from first-line fludarabine and prednisone and no benefit is derived from the addition of IFN-alpha to this regimen. The achievement of a good quality response to therapy was the only independent predictor of a prolonged response.
机译:背景与目的:氟达拉滨对慢性淋巴细胞性白血病(CLL)患者是一种有效的治疗方法,据报道干扰素-α(IFN-α)对CLL患者具有抗白血病活性。设计了一项随机研究,以评估在氟达拉滨和强的松一线治疗中添加IFN-α是否可以提高晚期CLL患者的缓解率,以及作为维持疗法的IFN-α是否可以改善缓解持续时间。设计与方法:133例患者被随机分配接受氟达拉滨(25 mg / m2 / iv,第9-13天)和泼尼松(20 mg / m2,第1、3、5、7和14、40和40 mg) / m2,第9至13天)(A组:66名患者),或除同一时间表外,IFN-alpha(2 MUI / sc,第1、3、5、7、9、11、13和15天)( B组:67名患者)。对治疗有反应的78位患者进入研究的缓解后阶段,其中41位患者被随机分配接受IFN-α(每周3次MUI 3次)和37位接受临床观察。结果:在两个组中观察到相似的缓解率(完全缓解+部分缓解):A组为86%,B组为84%(p = 0.4)。达到完全缓解的患者(p = 0.001)和接受IFN-α维持治疗的患者(p <0.05)观察到更长的缓解时间。但是,响应质量是影响响应持续时间的唯一重要且独立的因素(p <0.01)。就感染相关的死亡率和发病率而言,没有任何益处可归因于IFN-α的给药。解释和结论:在先前未接受治疗的患有晚期疾病的CLL患者中,一线氟达拉滨和泼尼松治疗的应答​​率高,并且在该方案中添加IFN-α并没有益处。对治疗的良好质量反应的实现是长期反应的唯一独立预测因子。

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