Zöchbauer S, Gsur A, Brunner R, Kyrle P A, Lechner K, Pirker R
Clinic for Internal Medicine I, University of Vienna Medical School, Austria.
Leukemia. 1994 Jun;8(6):974-7.
In order to further define the role of the MDR1 gene in acute myeloid leukemia (AML), we determined the association between the presence of P-glycoprotein on leukemic cells and the efficacy of therapy in patients with AML. Immunocytochemistry with monoclonal antibody C219 was performed to demonstrate the presence of P-glycoprotein. Positive staining ranged from 0 to 60% of the leukemic cells. For further analysis, patients were assigned into groups with 0-5% staining cells (group 1, n = 33) and with > 5% staining cells (group 2, n = 19). The complete remission rate of induction chemotherapy was 76% for group 1 but only 32% for group 2 (p = 0.002). The median duration of overall survival was 19 months for patients in group 1 as compared to 3 months for patients in group 2 (p = 0.007). The data indicate that P-glycoprotein expression is associated with an unfavorable prognosis in patients with AML.
为了进一步明确多药耐药基因1(MDR1)在急性髓系白血病(AML)中的作用,我们确定了白血病细胞上P-糖蛋白的存在与AML患者治疗疗效之间的关联。采用单克隆抗体C219进行免疫细胞化学检测以证实P-糖蛋白的存在。阳性染色范围为白血病细胞的0%至60%。为了进一步分析,将患者分为染色细胞为0%-5%的组(第1组,n = 33)和染色细胞>5%的组(第2组,n = 19)。第1组诱导化疗的完全缓解率为76%,而第2组仅为32%(p = 0.002)。第1组患者的总生存期中位数为19个月,而第2组患者为3个月(p = 0.007)。数据表明,P-糖蛋白表达与AML患者的不良预后相关。