青少年急性淋巴细胞白血病:一个新的“时代”。

James B Nachman
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引用次数: 0

摘要

与年轻患者相比,患有急性淋巴细胞白血病(ALL)的青少年具有更高的t细胞免疫表型发生率,更高的费城染色体阳性ALL发生率,更低的高二倍体和TEL-AML1易位发生率,以及更低的髓外肿物发病率。在10-15岁和16-21岁的患者之间似乎差别不大。与年轻患者相比,青少年ALL患者的无事件生存率(EFS)较低。在儿童ALL试验中治疗的16-21岁青少年的EFS明显优于成人试验。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,16-21岁青少年的四年EFS为73.1%。骨缺血性坏死是青少年急性淋巴细胞白血病治疗的一个重要并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adolescents with acute lymphoblastic leukemia: a new "age".

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.

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