T-cell pediatric acute lymphoblastic leukemia: analysis of survival and prognostic factors in 4 consecutive protocols of the Spanish cooperative study group SHOP

被引:7
|
作者
Rives, Susana [1 ]
Estella, Jesus
Camos, Mireia [1 ]
Garcia-Miguel, Purificacion [2 ]
Verdeguer, Amparo [3 ]
Miguel Couselo, Jose [4 ]
Tasso, Maria [5 ]
Molina, Javier [6 ]
Gomez, Pedro [7 ]
Fernandez-Delgado, Rafael [8 ]
Navajas, Aurora [9 ]
Badell, Isabel [10 ]
机构
[1] Univ Barcelona, Hosp St Joan de Deu, Hematol Lab, Barcelona, Spain
[2] Hosp La Paz, Madrid, Spain
[3] Hosp La Fe, Dept Hematooncol Pediat, E-46009 Valencia, Spain
[4] Hosp Xeral Galicia, Dept Hematooncol Pediat, La Coruna, Spain
[5] Hosp Univ Alicante, Dept Hematooncol Pediat, Alicante, Spain
[6] Hosp Virgen del Camino, Dept Hematooncol Pediat, Pamplona, Navarra, Spain
[7] Hosp Reina Sofia, Dept Hematooncol Pediat, Cordoba, Spain
[8] Hosp Clin Valencia, Dept Hematooncol Pediat, Valencia, Spain
[9] Hosp Cruces, Dept Hematooncol Pediat, Bilbao, Bizkaia, Spain
[10] Univ Autonoma Barcelona, Dept Hematooncol Pediat, Hosp Santa Creu & St Pau, E-08193 Barcelona, Spain
来源
MEDICINA CLINICA | 2012年 / 139卷 / 04期
关键词
T-cell acute lymphoblastic leukemia; Pediatric; Prognostic factors; MINIMAL RESIDUAL DISEASE; GENE-EXPRESSION; CLINICAL-SIGNIFICANCE; CHILDREN; PRECURSOR; PATHWAYS; SUBTYPES; THERAPY; DIFFERS; FUSION;
D O I
10.1016/j.medcli.2011.12.019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives: Acute lymphoblastic leukemia (ALL) is the most frequent cancer in childhood, with cure rates of 80-85%. In T-cell ALL (15% of ALL), prognostic factors are ill defined. We aimed to describe the event-free survival (EFS) and analyze clinical prognostic factors in a series of pediatric T-ALL of 4 consecutive clinical trials. Patients and methods: Children with T-ALL aged 1-18 years treated in 37 institutions in Spain were enrolled in 4 consecutive dials from February-1989 to November-2009. Results: A total of 218 T-ALL patients out of 1,652 pediatric ALL were evaluable during the study period (SHOP/ALL-89: 35, ALL-94: 63, ALL-99: 62, ALL-2005: 58). There were 164 boys (75%). Median age (years) was 7.8 range (1.3-18.6). Median leukocytes (10(9)/L) was 78.2, range 0.8-930. Fifteen (6.8%) children had central nervous system (CNS) involvement at diagnosis. Regarding response to induction treatment, 150 (75%) patients had less than 5% blasts on day-14 bone marrow and 199 achieved complete remission at the end of induction. Overall survival (OS) at 60 months for SHOP/ALL-89, ALL-94, ALL-99 was 48 (8), 49(6), 70 (6) %, respectively, and at 48 months for SHOP/ALL-2005 (ongoing protocol) was 74 (8) %. Median follow-up (months) was 206, 152, 74 and 17 respectively. Analysis of prognostic factors revealed no statistical differences regarding sex or age. Leukocyte count over 200 x 10(9)/l (P = .024), CNS infiltration at diagnosis (P < .006) and treatment response had prognostic significance (end-induction complete remission) (P = .0000), day 14-bone marrow (P = .005). Conclusions: Results for the SHOP/ALL-89 and ALL-94 protocols were inferior to other contemporary protocols but there has been an improvement in survival in the 2 last trials. In line with other T-ALL series, response to treatment had the strongest prognostic impact. (C) 2011 Elsevier Espana, S.L. All rights reserved.
引用
收藏
页码:141 / 149
页数:9
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