Thaler J
Universitätsklinik für Innere Medizin, Innsbruck.
Acta Med Austriaca. 1993;20(3):65-9.
In 1983 Talpaz et al. (43) for the first time demonstrated the efficacy of interferon-alpha (IFN-alpha) for the treatment of patients with chronic myelogenous leukemia (CML). This observation has been confirmed by several study groups in the consecutive years. An overview over the 7 largest trials including more than 400 patients reveals response rates (partial and complete hematological remissions) of 55 to 91%. In contrast to conventional chemotherapy IFN-alpha treatment resulted in a decrease of Philadelphia-chromosome positive metaphases (cytogenetic remissions) in 19 to 47% of these patients. A complete disappearance of the Philadelphia chromosome was found in 5 to 10% of patients. The following factors influence the response to IFN-alpha in patients with CML: phase and duration of the disease, several well defined risk factors, and IFN-dose. Currently available data are strongly suggestive for a survival benefit of patients with cytogenetic remissions, although definitive prove by phase-III trials is lacking. Actual studies focus on combinations of IFN-alpha and cytostatics, e.g. low-dose cytosine arabinoside.
1983年,塔尔帕兹等人(43)首次证明了α干扰素(IFN-α)治疗慢性粒细胞白血病(CML)患者的疗效。这一观察结果在随后几年得到了几个研究小组的证实。对包括400多名患者的7项最大规模试验的综述显示,缓解率(部分和完全血液学缓解)为55%至91%。与传统化疗不同,IFN-α治疗使19%至47%的此类患者费城染色体阳性中期相减少(细胞遗传学缓解)。5%至10%的患者费城染色体完全消失。以下因素影响CML患者对IFN-α的反应:疾病阶段和持续时间、几个明确的危险因素以及IFN剂量。目前可得的数据强烈提示细胞遗传学缓解的患者有生存获益,尽管缺乏III期试验的确切证据。目前的研究集中在IFN-α与细胞抑制剂的联合应用,例如小剂量阿糖胞苷。