Long-term results of Total Therapy studies 11, 12 and 13A for childhood acute lymphoblastic leukemia at St Jude Children's Research Hospital

被引:153
作者
Pui, CH
Boyett, JM
Rivera, GK
Hancock, ML
Sandlund, JT
Ribeiro, RC
Rubnitz, JE
Behm, FG
Raimondi, SC
Gajjar, A
Razzouk, B
Campana, D
Kun, LE
Relling, MV
Evans, WE
机构
[1] St Jude Childrens Res Hosp, Dept Hematoloncol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Pathol, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Biostat & Epidemiol, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Dept Pharmaceut Sci, Memphis, TN 38105 USA
[5] St Jude Childrens Res Hosp, Dept Radiat Oncol, Memphis, TN 38105 USA
[6] Univ Tennessee, Memphis, TN USA
[7] Coll Med, Memphis, TN USA
[8] Coll Pharm, Memphis, TN USA
关键词
CNS relapse; B-lineage ALL; T-lineage ALL; prognostic factors; leukemia; chemotherapy;
D O I
10.1038/sj.leu.2401938
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We present the long-term results of three consecutive clinical trials (Total Therapy studies 11, 12 and 13A) conducted far children with newly diagnosed acute lymphoblastic leukemia (ALL) between 1984 and 1994. In study 11 (1984-1988), the overall event-free survival rates (+/-1 s.e.) were 71.8+/-2.4% and 69.3 +/- 2.4%, and the cumulative risks of isolated central nervous system (CNS) relapse 5.6 +/- 1.2% and 5.9 +/- 1.3%, at 5 and 10 years, respectively. In study 12 (1988-1991), event-free survival rates were 67.6 +/- 3.4% and 61.5+/- 9.0%, and isolated CNS relapse rates were 10.4 +/- 2.3% and 10.4 +/-: 2.3%, respectively. Early intensive intrathecal therapy in study 13A (1991-1994) has yielded a very low 5-year isolated CNS relapse rate of 1.2+/-0.9%, boosting the 5-year event-free survival rate to 76.9 +/- 3.3%. Factors consistently associated with an adverse prognosis included male sex, infant or adolescent age group, leukocyte count >100 x 10(9)/l, nonhyperdiploidy karyotype and poor early response to treatment. Risk classification based on age and leukocyte count had prognostic significance in B-lineage hut not T-lineage ALL. Early therapeutic interventions or modifications for patients with specific genetic abnormalities or persistent minimal residual leukemia may further improve long-term results.
引用
收藏
页码:2286 / 2294
页数:9
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