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α干扰素联合小剂量阿糖胞苷治疗晚期慢性粒细胞白血病患者

Interferon-alpha plus low-dose cytosine arabinoside in advanced phase chronic myelogenous leukaemia patients.

作者信息

Ferrajoli A, Liberati A M, Caricchi P, Donti E, Morra E, Lazzarino M, Betti A R, Bernasconi P, Saglio G

机构信息

Department of Internal Medicine and Oncological Sciences, University of Perugia, Italy.

出版信息

Eur J Haematol. 1995 Sep;55(3):184-8. doi: 10.1111/j.1600-0609.1995.tb00248.x.

Abstract

Twenty-nine late chronic and accelerated phase chronic myelogenous leukaemia (CML) patients were entered in a pilot study designed to test the therapeutic efficacy of treatment with interferon-alpha (IFN-alpha) and low-dose cytosine arabinoside (ARA-C). IFN-alpha was administered at a dose of 2-10 x 10(6) IU/day and ARA-C at 15 mg/m2/day for 14 days each month. The treatment was well tolerated by 73% of the patients. Side effects were mainly asthenia, anorexia, anaemia and piastrinopenia. Haematological and cytogenetic responses were evaluated in the 19 patients who received more than 6 cycles. Four complete haematological response, 7 partial haematological response, 6 minor haematological response, 2 stable disease were obtained in this patient group. Two complete cytogenetic responses and 2 minor cytogenetic responses were detected in these patients. Suppression of secondary Ph' positive clones which appeared during the previous IFN-alpha treatment was documented in 3 accelerated phase patients after ARA-C was added to their IFN-alpha treatment. It would therefore seem that late chronic and accelerated phase CML patients benefit from combined IFN-alpha/ARA-C treatment and achieve haematological and cytogenetic responses not obtained during previous treatment without being exposed to undue toxicity. However, we cannot judge whether it offers any advantage in terms of survival.

摘要

29例晚期慢性期和加速期慢性粒细胞白血病(CML)患者进入一项初步研究,该研究旨在测试α-干扰素(IFN-α)和小剂量阿糖胞苷(ARA-C)联合治疗的疗效。IFN-α的给药剂量为2 - 10×10⁶IU/天,ARA-C为15mg/m²/天,每月各给药14天。73%的患者对该治疗耐受性良好。副作用主要为乏力、厌食、贫血和血小板减少。对接受超过6个周期治疗的19例患者评估了血液学和细胞遗传学反应。该患者组获得了4例完全血液学缓解、7例部分血液学缓解、6例微小血液学缓解、2例病情稳定。在这些患者中检测到2例完全细胞遗传学缓解和2例微小细胞遗传学缓解。在3例加速期患者中,于IFN-α治疗中加用ARA-C后,记录到之前IFN-α治疗期间出现的继发性Ph'阳性克隆受到抑制。因此,晚期慢性期和加速期CML患者似乎从IFN-α/ARA-C联合治疗中获益,并且获得了既往治疗中未达到的血液学和细胞遗传学反应,且未遭受过度毒性。然而,我们无法判断其在生存方面是否具有任何优势。

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