Antibody against poly(ethylene glycol) adversely affects PEG-asparaginase therapy in acute lymphoblastic leukemia patients

被引:554
作者
Armstrong, Jonathan K.
Hempel, Georg
Koling, Susanne
Chan, Linda S.
Fisher, Timothy
Meiselman, Herbert J.
Garratty, George
机构
[1] Univ So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USA
[2] Univ Munster, Inst Pharmaceut & Med Chem, D-4400 Munster, Germany
[3] Muenster Univ Clin, Clin Child & Adolescent Med Pediat Hematol & Onco, Munster, Germany
[4] Univ So Calif, Keck Sch Med, Dept Pediat, Los Angeles, CA USA
[5] Univ So Calif, Keck Sch Med, Dept Emergency Med, Los Angeles, CA USA
[6] Univ So Calif, Keck Sch Med, Dept Surg, Los Angeles, CA USA
[7] Amer Red Cross Blood Serv, Pomona, CA USA
关键词
lymphoblastic leukemia; antibody; poly(ethylene glycol); asparaginase medac; PEG-asparaginase; Oncaspar;
D O I
10.1002/cncr.22739
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Rapid clearance of poly(ethylene glycol)-asparaginase (PEG-ASNase) has been reported for up to one-third of patients treated for acute lymphoblastic leukemia (ALL), potentially rendering their treatment ineffective. A 25% occurrence of an antibody against PEG (anti-PEG) was previously reported in healthy blood donors. The objective of the study was to determine whether anti-PEG was associated with rapid clearance PEG-ASNase. METHODS. The investigation reanalyzed stored sera from pediatric patients enrolled in the ALL Berlin-Frankfurt-Muenster 2000 studies. Twenty-eight samples were selected to include 15 subjects with undetectable ASNase activity after receiving PEG-ASNase. Sixteen subjects treated with unmodified ASNase were also included, 8 with low ASNase activity. Sera were tested for anti-PEG using 2 techniques: 1) serology, by agglutination of PEG-coated red blood cells; 2) now cytometry, by analysis of 10 pm PEG beads stained for bound immunoglobulins. RESULTS. Of the 15 sera from PEG-ASNase-treated patients with undetectable ASNase activity, anti-PEG was detected in 9 by serology and in 12 by flow cytometry. Anti-PEG was detected in 1 PEG-ASNase-treated patient with lower ASNase activity (123 U/L). No relation was observed between anti-PEG and serum ASNase activity for patients treated with unmodified ASNase. CONCLUSIONS. The presence of anti-PEG was very closely associated with rapid clearance of PEG-ASNase. Further comprehensive studies are warranted to fully elucidate the effect of anti-PEG on PEG-conjugated agents. Screening and monitoring for anti-PEG may allow identification of patients for whom a modified dosing strategy or use of a non-PEGylated drug would be appropriate.
引用
收藏
页码:103 / 111
页数:9
相关论文
共 46 条
[1]  
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3582
[2]  
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3578
[3]  
Armstrong JK, 2003, BLOOD, V102, p556A
[4]  
Armstrong JK, 2003, BLOOD, V102, p94A
[5]   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
[6]   Pharmacokinetic/pharmacodynamic relationships of asparaginase formulations - The past, the present and recommendations for the future [J].
Avramis, VI ;
Panosyan, EH .
CLINICAL PHARMACOKINETICS, 2005, 44 (04) :367-393
[7]   Monitoring of asparaginase activity and asparagine levels in children on different asparaginase preparations [J].
Boos, J ;
Werber, G ;
Ahlke, E ;
SchulzeWesthoff, P ;
NowakGottl, U ;
Wurthwein, G ;
Verspohl, EJ ;
Ritter, J ;
Jurgens, H .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (09) :1544-1550
[8]   Monoclonal antibody-based quantitation of poly(ethylene glycol-derivatized proteins, liposomes, and nanoparticles [J].
Cheng, TL ;
Cheng, CM ;
Chen, BM ;
Tsao, DA ;
Chuang, KH ;
Hsiao, SW ;
Lin, YH ;
Roffler, SR .
BIOCONJUGATE CHEMISTRY, 2005, 16 (05) :1225-1231
[9]   Efficient clearance of poly(ethylene glycol)modified immunoenzyme with anti-PEG monoclonal antibody for prodrug cancer therapy [J].
Cheng, TL ;
Chen, BM ;
Chern, JW ;
Wu, MF ;
Roffler, SR .
BIOCONJUGATE CHEMISTRY, 2000, 11 (02) :258-266
[10]  
DELGADO C, 1992, CRIT REV THER DRUG, V9, P249