Abstract The chemotherapy agent L-asparaginase (L-asp) has been an important part of acute lymphoblastic leukemia therapy for over 30 years. It is evident that L-asp has a long-term curative effect. However, L-asp is associated with high incidence of adverse reactions. This has prompted the development of pegylated asparaginase (PEG-asp), which has undergone extensive testing. Apparently, PEG-asp has a prolonged half-life with a better tolerance profile while retaining the antileukemic effect. In this review, we attempt to outline the history of clinical application of L-asp, the pharmacological and clinical potential of various preparations of L-asp, the development of PEG-asp, and the clinical application and adverse events of PEG-asp. The literatures reviewed in this article is collected through online search of the major databases both in English and Chinese.
Masetti R, Pession A. First-line treatment of acute lymphoblastic leukemia with pegasparaginase[J]. Biologics, 2009, 3: 359-368.
[5]
Graham ML. Pegaspargase: a review of clinical studies[J]. Adv Drug Deliv Rev, 2003, 55(10): 1293-1302.
[6]
Broome JD. Evidence that the L-asparaginase of guinea pig serum is respnsible for its antilymhpoma effects and properties of the L-asparaginase of guinea pig serum in relation to those of the antilymphoma substance[J]. Exp Med, 1963, 118(1): 99-120.
[7]
Hann I, Vora A, Richards S, et al. Benefit of intensified treatment for all children with acute lymphoblastic leukaemia: results from MRC UKALL XI and MRC ALL97 randomised trials. UK Medical Research Council's Working Party on Childhood Leukaemia[J]. Leukemia, 2000, 14(3): 356-363.
[8]
Lee MB, Bridges JM. L-asparaginase activity in human and animal sera[J]. Nature (London), 1968, 217(5130): 758-759.
Narta UK, Kanwar SS, Azmi W. Pharmacological and clinical evaluation of L-asparaginase in the treatment of leukemia[J]. Crit Rev Oncol Hematol, 2007, 61(3): 208-221.
[11]
Mitchell L, Hoogendoorn H, Giles AR, et al. Increased endogenous thrombin generation in children with acute lymphoblastic leukemia: risk of thrombotic complications in L-asparaginase induced antithrombin Ⅲ deficiency[J]. Blood, 1994, 83(2): 386-391.
[12]
Savitri, Asthana N, Azmi W. Microbial l-asparaginase: a potent antitumor enzyme[J]. Indian Biotechnol, 2003, 2(2): 184-194.
[13]
Duval M, Suciu S, Ferster A, et al. Comparison of Escherichia coli-asparaginase with Erwinia-asparaginase in the treatment of childhood lymphoid malignancies: results of a randomized European Organisation for Research and Treatment of Cancer-Children's Leukemia Group phase 3 trial[J]. Blood, 2002, 99(8): 2734-2739.
[14]
Ho DH, Yap HY, Brown N, et al. Clinical pharmacology of intramuscularly administered l-asparginase[J]. Clin Pharmacol, 1981, 21(2):72-78.
[15]
Brueck M, Koerholz D, Nuernberger W, et al. Elimination of L-asparaginase in children treated for acute lymphoblastic leukemia[J]. Dev Pharmacol Ther, 1989, 12(4): 200-204.
[16]
Broome JD. Factors which may influence the effectiveness of L-asparaginases as tumor inhibitors[J]. Cancer, 1968, 22(3): 595-602.
[17]
Woo MH, Hak LJ, Storm MC, et al. Hypersensitivity or development of antibodies to asparaginase does not impact treatment outcome of childhood acute lymphoblastic leukemia[J]. Clin Oncol, 2000, 18(7): 1525-1532.
[18]
Otten J, Suciu S, Lutz P, et al. The importance of L-asparaginase (A'ase) in the treatment of acute lymphoblastic leukemia (ALL) in children: results of the EORTC 58881 randomized phase Ⅲ trial showing greater efficiency of E. coli (E. coli) as compared to Erwinia (Erw) A'ase[J]. Blood, 1996, 88(10): 2663-2663.
[19]
Pacquement H, Philippe N, Mechinaud F, et al. Importance of L-asparaginase (ASP), detrimental effects of additional cytosinearabinoside (ARA-C) and of iv 6-mercaptopurine (6-MP) in the treatment of lymphoblastic non-Hodgkin lymphoma (LB-NHL): results of the EORTC 58881 randomized trial[J]. SIOP XXIX, 1997, 160: 429.
[20]
Oettgen HF, Stephenson PA, Schwartz MR, et al. Toxicity of E. Coli l-asparaginase in man[J]. Cancer, 1970, 25(2): 253-278.
3.0.CO;2-U target="_blank">
[21]
Fabry U, Ktirholz D, Jfirgens H, et al. Anaphylaxis to L-asparaginase during treatment for acute lymphoblastic leukaemia in children-evidence of a complement mediated mechanism[J]. Pediatr Res, 1985, 19(4): 400-408.
[22]
Edman P, Nylen U, Sjoholm I. Dialysis membranes containing asparaginase entrapped in microparticles[J]. Methods Enzymol, 1988, 137: 491-496.
[23]
Lee JH, Kim SW, Sung KJ. Sagittal sinus thrombosis associated with transient free protein S deficiency after L-asparaginase treatment: case report and review of the literature[J]. Clin Neurol Neurosurg, 2000, 102(1): 33-36.
Vrooman LM, Supko JG, Neuberg DS, et al. Erwin ia asparaginase after allergy to E. coli asparaginase in children with acute lymphoblastic leuemia[J]. Pediatr Blood Cancer, 2010, 54(2): 199-205.
[26]
Lowas SR, Marks D, Malempati S. Prevalence of transient hyperglycemia during induction chemotherapy for pediatric acute lymphoblastic leukemia[J]. Pediatr Blood Cancer, 2009, 52(7): 814-818.
Aljabri K, Sirrs S, Nantel S. Hypertriglyceridemia and hypercholesterolemia induced by L-asparaginase[J]. Ann Saudi Med, 2003, 23(3-4): 173-174.
[30]
He YF, Wei W, Sun ZM, et al. Fatal lactic acidosis and hypoglycemia in a patient with relapsed natural killer/T-cell lymphoma[J]. Adv Ther, 2007, 24(3): 505-509.
[31]
Pasut G, Sergi M, Veronese FM. Anti-cancer PEG-enzymes: 30 years old, but still a current approach[J]. Adv Drug Deliv Rev, 2008, 60(1): 69-78.
[32]
Holle LM. Pegaspargase: an alternative?[J]. Ann Pharmacother, 1997, 31(5): 616-624.
[33]
Yamaoka T, Tabata Y, Ikada Y. Distribution and tissue uptake of poly(ethylene glycol) with different molecular `weights after intravenous administration to mice[J]. J Pharm Sci, 1994, 83(4): 601-606.
[34]
Silverman LB, Gelber RD, Dalton VK, et al. Improved outcome for children with acute lymphoblastic leukemia: results of Dana-Farber Consortium Protocol 91-01[J]. Blood, 2001, 97(5): 1211-1218.
[35]
Avramis VI, Sencer S, Periclou AP, et al. 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]. Blood, 2002, 99(6): 1986-1994.
[36]
Kurre HA, Ettinger AG, Veenstra DL, et al. Pharmacoeconomic analysis of pegaspargase versus native Escherichia coli L-asparaginase for the treatment of children with standard-risk, acute lymphoblastic leukemia: the Children's Cancer Group study (CCG-1962)[J]. Pediatr Hematol Oncol, 2002, 24(3):175-181.
[37]
Ettinger LJ, Kurtzberg J, Voute PA, et al. An open-label, multicenter study of polyethylene glycol-L-asparaginase for the treatment of acute lymphoblastic leukemia[J]. Cancer, 1995, 75(5): 1176-1181.
3.0.CO;2-Y target="_blank">
[38]
Silverman LB, Supko JG, Stevenson KE, et al. Intravenous PEG-asparaginase during remission induction in children and adolescents with newly diagnosed acute lymphoblastic leukemia[J]. Blood, 2010, 115(7): 1351-1353.
[39]
Keating GM. Asparaginase Erwinia chrysanthemi (Erwinaze®): a guide to its use in acute lymphoblastic leukemia in the USA[J]. BioDrugs, 2013, 27(4): 413-418.