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Substitution with doxorubicin for daunorubicin during induction for high risk pediatric acute lymphoblastic leukemia results in increased toxicity

机译:高危儿科急性淋巴细胞白血病诱导期间用阿霉素替代柔红霉素可增加毒性

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摘要

Widespread drug shortages have affected the availability of chemotherapy agents commonly used to treat pediatric ALL [1]. Induction chemotherapy for high risk acute lymphoblastic leukemia (HR ALL) consists of vincristine, PEG-aspargase, daunorubicin, and a glucocorticoid with associated low rates of morbidity and mortality, and a high rate of remission efficacy [2].The shortage of daunorubicin, which began in the spring of 2011, compromised the delivery of standard induction chemotherapy to pediatric HR-ALL patients. Daunorubicin and doxorubicin are historically considered dose equivalent in the treatment of ALL based upon in vitro testing showing similar sensitivity in untreated pediatric ALL samples [3].
机译:广泛的药物短缺影响了通常用于治疗小儿ALL的化疗药物的可用性[1]。高危急性淋巴细胞白血病(HR ALL)的诱导化疗由长春新碱,PEG-天冬酰胺酶,柔红霉素和糖皮质激素组成,具有较低的发病率和死亡率,且缓解率较高[2]。该疗法于2011年春季开始,影响了对小儿HR-ALL患者的标准诱导化疗的递送。根据体外试验显示,柔红霉素和阿霉素在ALL治疗中历来被视为剂量当量,在未治疗的儿科ALL样品中显示出相似的敏感性[3]。

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