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一项比较干扰素α与白消安治疗慢性粒细胞白血病的随机试验的长期随访。日本厚生省白血病研究组。

A long term follow-up of a randomized trial comparing interferon-alpha with busulfan for chronic myelogenous leukemia. The Kouseisho Leukemia Study Group.

作者信息

Ohnishi K, Tomonaga M, Kamada N, Onozawa K, Kuramoto A, Dohy H, Mizoguchi H, Miyawaki S, Tsubaki K, Miura Y, Omine M, Kobayashi T, Naoe T, Ohshima T, Hirashima K, Ohtake S, Takahashi I, Morishima Y, Naito K, Asou N, Tanimoto M, Sakuma A, Ohno R

机构信息

Department of Medicine III, Hamamatsu University School of Medicine, Japan.

出版信息

Leuk Res. 1998 Sep;22(9):779-86. doi: 10.1016/s0145-2126(98)00082-4.

Abstract

To evaluate the long-term effectiveness of interferon-alpha (IFN-alpha) therapy in patients with chronic myelogenous leukemia (CML) in chronic phase, we examined the updated outcomes of 159 patients who had been enrolled between 1988 and 1991 into a randomized trial comparing IFN-alpha with busulfan. At a median follow-up of 73 months, the median survival was 71 months in the IFN-alpha group and 55 months in the busulfan group (P=0.0563), and the median time of remaining in chronic phase was 58 months in the IFN-alpha group and 39 months in the busulfan group (P=0.4676). Landmark analysis showed a significant advantage in survival (P=0.009) and duration of chronic phase (P=0.0001) in patients with any cytogenetic response among the IFN-alpha group. About half patients were discontinued IFN-alpha administration in spite of cytogenetic response in this study. It appears that continuation of IFN-alpha might possibly confer a survival advantage. Pretreatment factors associated with cytogenetic response included high hemoglobin level, low percentage of peripheral basophils and low leukocyte counts. Multivariate analysis identified lower percentage of bone marrow basophilia (P=0.007) for survival advantage. If a group with a very good prognosis is predicted by a new prognostic model, it might be an option to wait for bone marrow transplantation.

摘要

为评估干扰素-α(IFN-α)治疗慢性期慢性粒细胞白血病(CML)患者的长期疗效,我们研究了1988年至1991年间纳入一项比较IFN-α与白消安的随机试验的159例患者的最新结局。在中位随访73个月时,IFN-α组的中位生存期为71个月,白消安组为55个月(P = 0.0563),IFN-α组的慢性期中位持续时间为58个月,白消安组为39个月(P = 0.4676)。标志性分析显示,IFN-α组中任何细胞遗传学反应的患者在生存(P = 0.009)和慢性期持续时间(P = 0.0001)方面具有显著优势。在本研究中,尽管有细胞遗传学反应,但仍有大约一半的患者停止了IFN-α治疗。似乎继续使用IFN-α可能会带来生存优势。与细胞遗传学反应相关的预处理因素包括高血红蛋白水平、外周血嗜碱性粒细胞百分比低和白细胞计数低。多变量分析确定较低的骨髓嗜碱性粒细胞百分比(P = 0.007)具有生存优势。如果通过新的预后模型预测出预后非常好的一组患者,等待骨髓移植可能是一种选择。

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