Comparison of Hypersensitivity Reactions to PEG-Asparaginase in Children After Intravenous and Intramuscular Administration

被引:22
作者
August, Keith J. [1 ]
Miller, Weston P. [2 ]
Dalton, Amanda [1 ]
Shinnick, Sara [3 ]
机构
[1] Childrens Mercy Hosp, Kansas City, MO 64108 USA
[2] Univ Minnesota, Div Blood & Marrow Transplant, Minneapolis, MN USA
[3] Sigma Tau Pharmaceut, Gaithersburg, MD USA
关键词
acute lymphoblastic leukemia; pediatrics; asparaginase; hypersensitivity reactions; ACUTE LYMPHOBLASTIC-LEUKEMIA; ESCHERICHIA-COLI ASPARAGINASE; INTENSIVE ASPARAGINASE; ERWINIA ASPARAGINASE; REMISSION INDUCTION; ALLERGIC REACTIONS; RISK; ANTIBODIES; ADULTS; ONCASPAR(TM);
D O I
10.1097/MPH.0b013e31828e5471
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction:Polyethylene-glycolated (PEG)-asparaginase (PEG-ASP) is a crucial component of pediatric acute lymphoblastic leukemia therapy. Although hypersensitivity reactions to PEG-ASP occur less frequently than with other formulations, they are not uncommon and have an adverse impact on patient outcomes. Intravenous (IV) administration of PEG-ASP reduces patient pain and anxiety and is being used with increasing frequency in children.Materials and Methods:A retrospective review was performed to compare the incidence of hypersensitivity reactions to PEG-ASP in children when administered either by intramuscular (IM) or IV routes between January 2006 and May 2008.Results:Of 68 patients studied, 7 experienced a hypersensitivity reaction (10.3%). Two of 16 patients (12.5%) who received only IV PEG-ASP and 3 of 27 patients (11.1%) exposed to only IM PEG-ASP experienced a hypersensitivity reaction. Severe reactions (grade 3 or 4) occurred only once after 119 total doses (0.8%) of IV PEG-ASP and once after 215 total doses (0.5%) of IM PEG-ASP (P=1.0). Thrombosis or pancreatitis were rare and were not increased after IV PEG-ASP administration.Discussion:IV PEG-ASP is well tolerated and does not result in a significant increase in the incidence of hypersensitivity reactions in children.
引用
收藏
页码:E283 / E286
页数:4
相关论文
共 34 条
[1]   Weekly polyethylene glycol conjugated L-asparaginase compared with biweekly dosing produces superior induction remission rates in childhood relapsed acute lymphoblastic leukemia: a pediatric oncology group study [J].
Abshire, TC ;
Pollock, BH ;
Billett, AL ;
Bradley, P ;
Buchanan, GR .
BLOOD, 2000, 96 (05) :1709-1715
[2]   Intensive high-dose asparaginase consolidation improves survival for pediatric patients with T cell acute lymphoblastic leukemia and advanced stage lymphoblastic lymphoma: a Pediatric Oncology Group study [J].
Amylon, MD ;
Shuster, J ;
Pullen, J ;
Berard, C ;
Link, MP ;
Wharam, M ;
Katz, J ;
Yu, A ;
Laver, J ;
Ravindranath, Y ;
Kurtzberg, J ;
Desai, S ;
Camitta, B ;
Murphy, SB .
LEUKEMIA, 1999, 13 (03) :335-342
[3]   COMPARATIVE PHARMACOKINETIC STUDIES OF 3 ASPARAGINASE PREPARATIONS [J].
ASSELIN, BL ;
WHITIN, JC ;
COPPOLA, DJ ;
RUPP, IP ;
SALLAN, SE ;
COHEN, HJ .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (09) :1780-1786
[4]   A randomized comparison of native Escherichia coli asparaginase and polyethylene glycol conjugated asparaginase for treatment of children with newly diagnosed standard-risk acute lymphoblastic leukemia:: a Children's Cancer Group study [J].
Avramis, VI ;
Sencer, S ;
Periclou, AP ;
Sather, H ;
Bostrom, BC ;
Cohen, LJ ;
Ettinger, AG ;
Ettinger, LJ ;
Franklin, J ;
Gaynon, PS ;
Hilden, JM ;
Lange, B ;
Majlessipour, F ;
Mathew, P ;
Needle, M ;
Neglia, J ;
Reaman, G ;
Holcenberg, JS .
BLOOD, 2002, 99 (06) :1986-1994
[5]  
BILLETT AL, 1992, CANCER, V70, P201, DOI 10.1002/1097-0142(19920701)70:1<201::AID-CNCR2820700131>3.0.CO
[6]  
2-M
[7]  
CHEUNG NKV, 1986, AM J PEDIAT HEMATOL, V8, P99
[8]   4-AGENT INDUCTION AND INTENSIVE ASPARAGINASE THERAPY FOR TREATMENT OF CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA [J].
CLAVELL, LA ;
GELBER, RD ;
COHEN, HJ ;
HITCHCOCKBRYAN, S ;
CASSADY, JR ;
TARBELL, NJ ;
BLATTNER, SR ;
TANTRAVAHI, R ;
LEAVITT, P ;
SALLAN, SE .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (11) :657-663
[9]  
DELLINGER CT, 1976, CANCER-AM CANCER SOC, V38, P1843, DOI 10.1002/1097-0142(197610)38:4<1843::AID-CNCR2820380463>3.0.CO
[10]  
2-J