Nachman James B
Pritzger School of Medicine, University of Chicago, USA.
Rev Clin Exp Hematol. 2003 Sep;7(3):261-9.
Adolescents with acute lymphoblastic leukemia (ALL) have a higher incidence of T-cell immunophenotype, a higher incidence of Philadelphia chromosome positive ALL, a lower incidence of high hyperdiploidy and TEL-AML1 translocation, and a lower incidence of extramedullary bulk disease compared to younger patients. There appears to be little difference between 10-15 and 16-21 year old patients. Adolescents with ALL have a lower event free survival (EFS) compared to younger patients. Adolescents 16-21 years of age treated on pediatric ALL trials have a significantly better EFS than those treated on adult trials. Pediatric treatment protocols utilize more vincristine, steroid and L-asparaginase compared to adult trials. In a recently completed Children's Cancer Group trial, adolescents 16-21 years of age had a four-year EFS of 73.1%. Avascular necrosis of bone is an important complication of therapy in adolescents with ALL.
与较年轻患者相比,急性淋巴细胞白血病(ALL)青少年患者的T细胞免疫表型发生率更高、费城染色体阳性ALL的发生率更高、高超二倍体和TEL-AML1易位的发生率更低,以及髓外肿块病的发生率更低。10至15岁和16至21岁患者之间似乎没有太大差异。ALL青少年患者的无事件生存率(EFS)低于较年轻患者。在儿科ALL试验中接受治疗的16至21岁青少年的EFS明显优于在成人试验中接受治疗的患者。与成人试验相比,儿科治疗方案使用更多的长春新碱、类固醇和L-天冬酰胺酶。在最近完成的儿童癌症组试验中,16至21岁青少年的四年EFS为73.1%。骨缺血性坏死是ALL青少年患者治疗的重要并发症。