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Guidelines for Complications of Cancer Treatment Vol VIII Part B

Guidelines for Complications of Cancer Treatment Vol VIII Part B

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4. Efficacy and safety <strong>of</strong> rasburicase, a recombinanturate oxidase (Elitek), in the management <strong>of</strong>malignancy-associated hyperuricemia inpediatric and adult patients: final results <strong>of</strong> amulticenter compassionate use trial.Jeha S, Kantarjian H, Irwin D, et al. Leukemia.2005;19:34-8.The recombinant urate oxidase, rasburicase (Elitek, San<strong>of</strong>i-Synthelabo, Inc.), has recently received regulatory approval<strong>for</strong> the prevention and treatment <strong>of</strong> hyperuricemia in childrenwith leukemia, lymphoma, and solid tumors. Prior to approval,682 children and 387 adults in the US and Canada receivedrasburicase on compassionate-use basis. Uric acidconcentration declined rapidly in both adult and pediatricpatients after rasburicase treatment. Similar responses wereobserved in patients treated with subsequent courses. Possibledrug-related adverse events, including allergic reactions, wereuncommon. These data confirm that rasburicase is effectiveand safe <strong>for</strong> the treatment and prophylaxis <strong>of</strong> children andadults with malignancy-associated hyperuricemia.5. Reduced-dose rasburicase (recombinantxanthine oxidase) in adult cancer patients withhyperuricemia.Trifilio S, Gordon L, Singhal S, et al Bone MarrowTransplant. 2006;37:997-1001.Recombinant urate oxidase (rasburicase) lowers uric acidlevels rapidly to very low levels at the labeled dose <strong>of</strong> 0.15-0.2 mg/kg daily <strong>for</strong> 5 days. Our past experience showed that alower dose (3 mg) lowered uric acid levels sufficiently in mostpatients. A retrospective review was conducted to determinethe effect <strong>of</strong> a fixed 3 mg dose <strong>of</strong> rasburicase in 43 adult patientswith cancer undergoing hematopoietic stem cell transplantationor receiving chemotherapy who had elevated or rising uric439

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