Hehlmann R, Heimpel H, Hasford J, Kolb H J, Pralle H, Hossfeld D K, Queisser W, Löffler H, Heinze B, Georgii A
Klinikum Mannheim, Universität Heidelberg, Mannheim, Deutschland.
Blood. 1993 Jul 15;82(2):398-407.
In a randomized multicenter study the influence of hydroxyurea versus busulfan on the duration of the chronic phase and on survival of chronic myelogenous leukemia (CML) was determined. In addition cross resistance and adverse reactions of the drugs were analyzed. From July 1983 to January 1991, 441 CML patients were randomized to receive hydroxyurea or busulfan. Of these, 90.7% were Philadelphia positive; 25.7% were low, 38.2% intermediate, and 36.2% high risk patients according to Sokal's score. The median survival of the busulfan treated Philadelphia-positive patients is 45.4 months and of the hydroxyurea group 58.2 months (P = .008). The survival advantage for the hydroxyurea treated patients is recognized in all risk groups. Sixty four patients reached therapy resistance before blast crisis and were crossed over to the alternative drug. The 23 patients with primary hydroxyurea had a median survival of 5.6 years, the 41 patients with primary busulfan therapy a median survival of 2.7 years (P = .02). Adverse reactions were less frequent with hydroxyurea with no severe adverse effects (lung fibrosis, long lasting bone marrow aplasia). The analysis of white blood cell counts in the course of treatment showed lower counts in the hydroxyurea patients. We conclude that hydroxyurea is superior to busulfan in therapy of CML in chronic phase and should be used as first line therapy. Busulfan may have a role as secondary therapy after hydroxyurea resistance or intolerance.
在一项随机多中心研究中,确定了羟基脲与白消安对慢性粒细胞白血病(CML)慢性期持续时间和生存率的影响。此外,还分析了药物的交叉耐药性和不良反应。从1983年7月至1991年1月,441例CML患者被随机分配接受羟基脲或白消安治疗。其中,90.7%为费城染色体阳性;根据索卡尔评分,25.7%为低危、38.2%为中危、36.2%为高危患者。接受白消安治疗的费城染色体阳性患者的中位生存期为45.4个月,羟基脲组为58.2个月(P = 0.008)。在所有风险组中均认识到羟基脲治疗患者的生存优势。64例患者在急变期前出现治疗耐药并改用替代药物。23例初始接受羟基脲治疗的患者中位生存期为5.6年,41例初始接受白消安治疗的患者中位生存期为2.7年(P = 0.02)。羟基脲的不良反应较少,且无严重不良反应(肺纤维化、长期骨髓抑制)。治疗过程中的白细胞计数分析显示羟基脲治疗患者的白细胞计数较低。我们得出结论,在慢性期CML治疗中,羟基脲优于白消安,应作为一线治疗药物。白消安可在羟基脲耐药或不耐受后作为二线治疗药物。