Hoelzer D F
Department of Hematology, University of Frankfurt, Germany.
Hematol Oncol Clin North Am. 1993 Feb;7(1):139-60.
Results for adult ALL have improved, with CR rates of 68% to 91% and a cure rate of 25% to 41%. The outcome for patients with T-ALL has especially improved, and the major drugs responsible are C and ara-C. Outcome for B-ALL has improved by using short intensive cycles including, among other drugs, C and high-dose MTX. The inferior outcome of adult ALL compared with childhood ALL seems related to the high proportion of Ph1/BCR-ABL positive ALL patients, which constitute about 30% in adults versus less than 5% in children. The major prognostic factors for survival in adult ALL are age, time to achieve CR, cytogenetic abnormalities, immunologic subtype, and WBC; these may serve as a guide for BMT in first CR. New approaches in the treatment of adult ALL include the use of HGFs, the use of biologic response modifiers, and the detection of MRD to tailor treatment decisions.
成人急性淋巴细胞白血病(ALL)的治疗结果有所改善,完全缓解(CR)率为68%至91%,治愈率为25%至41%。T-ALL患者的治疗结果尤其得到改善,主要药物是环磷酰胺(C)和阿糖胞苷(ara-C)。通过使用包括C和大剂量甲氨蝶呤(MTX)等药物的短期强化疗程,B-ALL的治疗结果得到改善。与儿童ALL相比,成人ALL较差的治疗结果似乎与Ph1/BCR-ABL阳性ALL患者的高比例有关,该比例在成人中约为30%,而在儿童中不到5%。成人ALL生存的主要预后因素包括年龄、达到CR的时间、细胞遗传学异常、免疫亚型和白细胞计数;这些因素可作为首次完全缓解时进行骨髓移植(BMT)的指导。成人ALL治疗的新方法包括使用造血生长因子(HGFs)、使用生物反应调节剂以及检测微小残留病(MRD)以制定治疗决策。