Raza A, Gezer S, Anderson J, Lykins J, Bennett J, Browman G, Goldberg J, Larson R, Vogler R, Preisler H D
Roswell Park Memorial Institute, Buffalo, New York.
Exp Hematol. 1992 Nov;20(10):1194-200.
Pretherapy bone marrow (BM) aspirates of 143 patients with acute myeloid leukemia (AML) were incubated simultaneously with bromodeoxyuridine (BrdU) and tritiated cytosine arabinoside ([3H]Ara-C) to determine the labeling index (LI) and extent of [3H]Ara-C incorporation. Of 143 AML patients, 121 received high-dose Ara-C (HDAra-C) as a single agent for induction therapy (55 newly diagnosed, 66 in first relapse), whereas 22 received HDAra-C plus mAMSA. The data demonstrate that a subset of patients who will fail HDAra-C remission induction therapy because of drug-resistant disease can be prospectively identified on the basis of the low amount of Ara-C incorporated by their leukemia cells.
对143例急性髓系白血病(AML)患者的治疗前骨髓抽吸物同时与溴脱氧尿苷(BrdU)和氚标记的阿糖胞苷([3H]Ara-C)一起孵育,以确定标记指数(LI)和[3H]Ara-C掺入程度。143例AML患者中,121例接受大剂量阿糖胞苷(HDAra-C)作为单一诱导治疗药物(55例新诊断患者,66例首次复发患者),而22例接受HDAra-C加胺苯吖啶治疗。数据表明,由于耐药性疾病而将在HDAra-C缓解诱导治疗中失败的一部分患者可根据其白血病细胞掺入阿糖胞苷的量少而被前瞻性地识别出来。