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首页> 外文期刊>Hematological oncology >Low-dose oral fludarabine plus cyclophosphamide in elderly patients with untreated and relapsed or refractory chronic lymphocytic Leukaemia.
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Low-dose oral fludarabine plus cyclophosphamide in elderly patients with untreated and relapsed or refractory chronic lymphocytic Leukaemia.

机译:低剂量口服氟达拉滨加环磷酰胺治疗未治疗,复发或难治性慢性淋巴细胞性白血病的老年患者。

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Fludarabine plus cyclophosphamide (FC) at conventional doses is an effective treatment for chronic lymphocytic leukaemia (CLL). However, FC at standard doses may give hematological and non-hematological toxicity, predominantly in the elderly. Intravenous or oral low-dose FC regimens remain highly effective in elderly patients with Low-Grade Lymphomas other than CLL and are well tolerated. We tested efficacy and toxicity of oral FC at reduced doses in 26 elderly patients (median 71 years) with previously untreated (UT-CLL, n = 14) or relapsed/refractory CLL (R-CLL, n = 12), unfit for conventional treatments. Twentyfour-of-26 (92%) patients (14/14, 100% UT-CLL; 10/12, 83.5% R-CLL) obtained a response, with 12/26 (46%) complete responses (9/14, 64.2% in UT-CLL; 3/12, 25% in R-CLL). Non-hematological toxicity was mild and myelosuppression was documented in 8/26 (31%) patients (4/14, 28% UT-CLL; 4/12, 33% R-CLL). With a median follow-up of 24 months, median event-free survival was 48 months with no differences between UT-CLL and R-CLL and all responders were alive. Low-dose oral FC treatment showed good efficacy in both untreated and refractory/relapsed CLL. The treatment is useful in elderly patients who cannot benefit of more aggressive schedules and is easy to administer on an outpatient basis. Copyright (c) 2008 John Wiley & Sons, Ltd.
机译:常规剂量的氟达拉滨加环磷酰胺(FC)是治疗慢性淋巴细胞性白血病(CLL)的有效方法。但是,标准剂量的FC可能会引起血液学和非血液学毒性,主要发生在老年人中。静脉或口服低剂量FC方案对除CLL以外的低级淋巴瘤的老年患者仍然有效,并且耐受性良好。我们测试了26例先前未接受过治疗(UT-CLL,n = 14)或复发/难治性CLL(R-CLL,n = 12),不适合常规治疗的老年患者(降低剂量)口服FC的疗效和毒性治疗。 26个患者中有24个(92%)(14 / 14,100%UT-CLL; 10 / 12,83.5%R-CLL)获得了缓解,其中12/26(46%)个完全缓解(9/14, UT-CLL为64.2%; R / CLL为3 / 12,25%)。非血液学毒性轻微,在8/26(31%)患者中记录了骨髓抑制(4 / 14,28%UT-CLL; 4 / 12,33%R-CLL)。中位随访期为24个月,中位无事件生存期为48个月,UT-CLL和R-CLL之间无差异,所有应答者均存活。低剂量口服FC治疗在未治疗和难治性/复发性CLL中均显示出良好的疗效。该疗法对无法从更积极的治疗方案中受益的老年患者很有用,并且易于在门诊患者基础上给药。版权所有(c)2008 John Wiley&Sons,Ltd.

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