Gemtuzumab ozogamicin:: first clinical experiences in children with relapsed/refractory acute myeloid leukemia treated on compassionate-use basis

被引:75
作者
Zwaan, CM
Reinhardt, D
Corbacioglu, S
van Wering, ER
Bökkerink, JPM
Tissing, WJE
Samuelsson, U
Feingold, J
Creutzig, U
Kaspers, GJL
机构
[1] Free Univ Amsterdam, Ctr Med, Dept Pediat Hematol Oncol, NL-1081 HV Amsterdam, Netherlands
[2] Univ Munster, Childrens Hosp, AML BFM Study Grp, D-4400 Munster, Germany
[3] Dutch Childhood Oncol Grp, The Hague, Netherlands
[4] Univ Ulm, Dept Pediat, D-7900 Ulm, Germany
[5] Univ Nijmegen, Med Ctr St Radboud, Dept Pediat Hematooncol, Nijmegen, Netherlands
[6] Erasmus Univ, Ctr Med, Sophia Childrens Hosp, Dept Pediat Oncol, Rotterdam, Netherlands
[7] Wyeth Pharmaceut, St Davids, PA USA
[8] Linkoping Univ, Dept Hlth & Environm, Div Pediat, Linkoping, Sweden
关键词
D O I
10.1182/blood-2002-07-1947
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gemtuzumab ozogamicin (GO; Mylotarg) was developed to treat CD33(+) acute myeloid leukemia (AML). To date, only studies in adults and preliminary data from a phase 1 study in children have been reported. We report data on 15 children with relapsed/refractory CD33(+) AML who were treated with GO I monotherapy on compassionate use basis (4-9 mg/m(2) up to 3 courses). Eight children showed a reduction in bone marrow blasts to 6% or less, including 5 in complete remission without full platelet recovery, (CRp). Three of the 5 children with CRp received transplants almost directly following the last GO course, without awaiting further platelet regeneration. Hence in these children no clear discrimination bet tween complete remission (CR) and CRp could be made. In 6 of 8 responding patients further treatment was given. consisting of stem cell transplantation (SCT). Two patients are still alive, currently 6 and 9 months after SCT. Hematologic toxicity was difficult to assess due to subsequent SCT or leukemia. tide effects, in one patient each included veno-occlusive disease, transient grade 3 hyperbilirubinemia, transient grade 3 transaminase elevation, And grade 3 hypo-tension during GO administration. No infections or mucositis occurred. This report demonstrates clinical efficacy of GO in a subset of relapsed/refractory pediatric CD33(+) AML patients and suggests that intensive postremission therapy after remission induction by GO may. result in durable responses in some patients, although follow-up is-still short. Further studies are needed to determine the efficacy and safety of GO in children with AML. (C) 2003 by The American Society of Hematology.
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页码:3868 / 3871
页数:4
相关论文
共 14 条
[1]  
Bross PF, 2001, CLIN CANCER RES, V7, P1490
[2]  
CREUTZIG U, 1995, BLOOD, V86, P3097
[3]  
Fleischhack G, 1998, BRIT J HAEMATOL, V102, P647
[4]  
Giles FJ, 2001, CANCER-AM CANCER SOC, V92, P406, DOI 10.1002/1097-0142(20010715)92:2<406::AID-CNCR1336>3.0.CO
[5]  
2-U
[6]  
HINMAN LM, 1993, CANCER RES, V53, P3336
[7]  
Jilani I, 2001, BLOOD, V98, p586A
[8]  
Larson RA, 2002, BLOOD, V100, p338A
[9]   Hepatic sinusoidal obstruction after gemtuzumab ozogamicin (Mylotug) therapy [J].
Rajvanshi, P ;
Shulman, HM ;
Sievers, EL ;
McDonald, GB .
BLOOD, 2002, 99 (07) :2310-2314
[10]   Selective ablation of acute myeloid leukemia using antibody-targeted chemotherapy: A phase I study of an anti-CD33 calicheamicin immunoconjugate [J].
Sievers, EL ;
Appelbaum, FR ;
Spielberger, RT ;
Forman, SJ ;
Flowers, D ;
Smith, FO ;
Shannon-Dorcy, K ;
Berger, MS ;
Bernstein, ID .
BLOOD, 1999, 93 (11) :3678-3684