Dexamethasone versus prednisone for induction therapy in childhood acute lymphoblastic leukemia: a systematic review and meta-analysis

被引:76
作者
Teuffel, O. [1 ]
Kuster, S. P. [2 ]
Hunger, S. P. [3 ,4 ]
Conter, V. [5 ,6 ]
Hitzler, J. [1 ]
Ethier, M-C
Shah, P. S. [7 ,8 ]
Beyene, J. [8 ,9 ,10 ]
Sung, L. [1 ,8 ]
机构
[1] Hosp Sick Children, Div Haematol Oncol, Toronto, ON M5G 1X8, Canada
[2] Mt Sinai Hosp, Dept Microbiol, Toronto, ON M5G 1X5, Canada
[3] Univ Colorado Denver Sch Med, Childrens Hosp, Aurora, CO USA
[4] Univ Colorado Denver Sch Med, Dept Pediat, Aurora, CO USA
[5] Univ Milano Bicocca, Dept Pediat, Osped San Gerardo, Monza, Italy
[6] Osped Riuniti Bergamo, Dept Pediat, I-24100 Bergamo, Italy
[7] Mt Sinai Hosp, Dept Pediat, Toronto, ON M5G 1X5, Canada
[8] Univ Toronto, Dept Hlth Policy Management & Evaluat, Toronto, ON, Canada
[9] Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada
[10] McMaster Univ, Dept Clin Epidemiol, Hamilton, ON L8S 4L8, Canada
基金
加拿大健康研究院;
关键词
childhood leukemia; corticosteroids; treatment; toxicity; STANDARD-RISK; CHILDREN; GLUCOCORTICOIDS; TRIAL; ALL97;
D O I
10.1038/leu.2011.84
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This systematic review and meta-analysis compared the efficacy and toxicity of dexamethasone (DEX) versus prednisone (PRED) for induction therapy in childhood acute lymphoblastic leukemia (ALL). We searched biomedical literature databases and conference proceedings for randomized controlled trials comparing DEX and PRED during induction therapy for childhood ALL. A total of eight studies were eligible for inclusion in this meta-analysis. DEX, in comparison with PRED, reduced events (that is, death from any cause, refractory or relapsed leukemia, or second malignancy; risk ratio (RR) 0.80; 95% confidence interval (CI), 0.68-0.94) and central nervous system relapse (RR 0.53; 95% CI, 0.44-0.65), but did not alter bone marrow relapse (RR 0.90; 95% CI, 0.69-1.18) or overall mortality (RR 0.91; 95% CI, 0.76-1.09). Patients receiving DEX had a higher risk of mortality during induction (RR 2.31; 95% CI, 1.46-3.66), neuro-psychiatric adverse events (RR 4.55; 95% CI, 2.45-8.46) and myopathy (RR 7.05; 95% CI, 3.00-16.58). There was no statistically significant difference in the risk of osteonecrosis, sepsis, fungal infection, diabetes or pancreatitis. DEX in induction therapy for children with ALL is more efficacious than PRED. However, DEX is also associated with more toxicity, and currently it remains unclear whether short-term superiority of DEX will also result in better overall survival. Leukemia (2011) 25, 1232-1238; doi:10.1038/leu.2011.84; published online 29 April 2011
引用
收藏
页码:1232 / 1238
页数:7
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