Mantadakis Elpis, Danilatou Vassiliki, Stiakaki Eftichia, Kalmanti Maria
Department of Pediatric Hematology/Oncology, University Hospital of Heraklion, Heraklion, Crete, Greece.
Pediatr Hematol Oncol. 2004 Jan-Feb;21(1):27-35.
Traditionally, children with acute lymphoblastic leukemia receive prednisone, as part of multiagent remission-induction chemotherapy. Recently, many cooperative groups use dexamethasone instead of prednisone during induction. We describe the infectious toxicities experienced by the first two patients in our institution treated with dexamethasone (10 mg/m(2)/day for 4 weeks with gradual tapering) during induction according to the dexamethasone arm of BFM 2000 and review the relevant literature that suggests an increased risk of infectious complications with dexamethasone. Only a prospective two-arm ALL dexamethasone study at two dose levels (6 and 10 mg/m(2)/day) will clarify if indeed the higher dose of dexamethasone during induction is more effective and without unacceptable toxicity.
传统上,急性淋巴细胞白血病患儿接受泼尼松治疗,作为多药联合缓解诱导化疗的一部分。最近,许多协作组在诱导治疗期间使用地塞米松而非泼尼松。我们描述了我院按照BFM 2000地塞米松组方案在诱导治疗期间接受地塞米松(10 mg/m²/天,共4周,逐渐减量)治疗的前两名患者所经历的感染性毒性反应,并回顾了相关文献,这些文献提示地塞米松会增加感染并发症的风险。只有一项前瞻性双臂全剂量地塞米松研究,在两个剂量水平(6和10 mg/m²/天)下进行,才能明确诱导治疗期间较高剂量的地塞米松是否确实更有效且无不可接受的毒性。