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首页> 外文期刊>Leukemia: Official journal of the Leukemia Society of America, Leukemia Research Fund, U.K >Dexamethasone versus prednisone for induction therapy in childhood acute lymphoblastic leukemia: a systematic review and meta-analysis.
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Dexamethasone versus prednisone for induction therapy in childhood acute lymphoblastic leukemia: a systematic review and meta-analysis.

机译:地塞米松与泼尼松诱导治疗儿童急性淋巴细胞白血病:系统评价和荟萃分析。

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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.
机译:本系统评价和荟萃分析比较了地塞米松 (DEX) 与泼尼松 (PRED) 诱导治疗儿童急性淋巴细胞白血病 (ALL) 的疗效和毒性。我们检索了生物医学文献数据库和会议论文集,以寻找比较DEX和PRED在儿童ALL诱导治疗期间的随机对照试验。共有8项研究符合纳入本荟萃分析的条件。与PRED相比,DEX减少了事件(即任何原因导致的死亡、难治性或复发性白血病或第二恶性肿瘤;风险比(RR)0.80;95%置信区间(CI),0.68-0.94)和中枢神经系统复发(RR 0.53;95%CI,0.44-0.65),但没有改变骨髓复发(RR 0.90;95%CI,0.69-1.18)或总死亡率(RR 0.91;95%CI, 0.76-1.09). 接受DEX治疗的患者在诱导期间死亡风险更高(RR 2.31;95% CI,1.46-3.66)、神经精神不良事件(RR 4.55;95% CI,2.45-8.46)和肌病(RR 7.05;95% CI,3.00-16.58)。骨坏死、败血症、真菌感染、糖尿病或胰腺炎的风险无统计学意义差异。DEX 在 ALL 患儿诱导治疗中的疗效高于 PRED。然而,DEX也与更多的毒性有关,目前尚不清楚DEX的短期优势是否也会导致更好的总生存期。

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