期刊
BRITISH JOURNAL OF HAEMATOLOGY
卷 153, 期 1, 页码 58-65出版社
WILEY-BLACKWELL
DOI: 10.1111/j.1365-2141.2011.08588.x
关键词
childhood leukaemia; erythrocytes; leukaemia; new drugs for leukaemia
类别
P>l-asparaginase encapsulated within erythrocytes (GRASPA (R)) should allow serum asparagine depletion over a longer period than the native form of the enzyme, using lower doses and allowing better tolerance. The GRASPALL 2005-01 study, a multicentre randomized controlled trial, investigated three doses of GRASPA (R) for the duration of asparagine depletion in a phase I/II study in adults and children with acute lymphoblastic leukaemia (ALL) in first relapse. Between February 2006 and April 2008, 18 patients received GRASPA (R) (50 iu/kg: n = 6, 100 iu/kg: n = 6, 150 iu/kg: n = 6) after randomization, and six patients were assigned to the Escherichia coli native l-asparaginase (E. colil-ASNase) control group. GRASPA (R) was effective at depleting l-asparagine. One single injection of 150 iu/kg of GRASPA (R) provided similar results to 8 x 10 000 iu/m2 intravenous injections of E. colil-ASNase. The safety profile of GRASPA (R) showed a reduction in the number and severity of allergic reactions and a trend towards less coagulation disorders. Other expected adverse events were comparable to those observed with E. colil-ASNase and there was also no difference between the three doses of GRASPA (R).
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