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18 - Prediction of therapeutic index of antibody-based therapeutics: mathematical modeling approaches

from II - INTEGRATED APPROACHES OF PREDICTIVE TOXICOLOGY

Published online by Cambridge University Press:  06 December 2010

Jinghai J. Xu
Affiliation:
Merck Research Laboratory, New Jersey
Laszlo Urban
Affiliation:
Novartis Institutes for Biomedical Research, Massachusetts
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Summary

Biologics represent a landmark shift in the pharmaceutical industry. The global market for human medicines was $750 billion and global sales of biologic medicines were $87 billion in 2008. Monoclonal antibodies (mAbs) represented one of the most important classes of biologics with sales of $33 billion. Remicade (infliximab; Centocor) for Crohn's disease was the market leader, followed by Rituxan (rituximab; Genentech) for non-Hodgkin's lymphoma, Herceptin (trastuzumab; Genentech) for HER2–positive breast cancer, Avastin (bevacizumab; Genentech) for colorectal cancer, Humira (adalimumab; Abbott) for rheumatoid arthritis, Synagis (palivizumab; Medimmune) for pediatric respiratory disease, and Erbitux (cetuximab; Imclone Systems) for colorectal cancer. The growing interest in using mAbs as therapeutics lies in their exquisite specificity for the target antigen. Unlike small-molecule therapeutics, which almost always show off-target effects due to overlapping activities against related members of enzyme families, antibodies can be targeted to individual protein targets. High specificity of antibody–antigen interaction can lead to a desirable therapeutic with high efficacy with minimal nontarget side effects.

MATHEMATICAL MODELING IN DRUG DISCOVERY

Mathematical modeling in the pharmaceutical industry has been done traditionally in the pharmacokinetic, pharmacodynamics, and drug metabolism groups. Researchers in these groups employ the tools of pharmacokinetic-pharmacodynamic (PKPD) modeling. Generally, a model is picked to best fit the animal data, and this model is used for translation from animal to human data for dose predictions based on allometric scaling (i.e., parameters of the models are scaled based on body weights of the species).

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Publisher: Cambridge University Press
Print publication year: 2010

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References

Maggon, K. Global pharmaceutical market review & world top ten/twenty drugs 2008. http://knol.google.com/k/krishan-maggon/global-pharmaceutical-market-review/ 3fy5eowy8suq3/6# Accessed March 28, 2009.
Aggarwal, S. What's fueling the biotech engine?Nat Biotech. 2007;25(10):1097–1104.CrossRefGoogle ScholarPubMed
Derendorf, H, Meibohm, B. Modeling of pharmacokinetic/pharmacodynamic (PK/PD) relationships: Concepts and perspectives. Pharma Res. 1999;16(2):176–185.CrossRefGoogle Scholar
Gibaldi, M, Perrier, D. Pharmacokinetics. 2nd ed.New York, NY: Informa HealthCare; 1982.Google Scholar
Rowland, M, Tozer, TN. Clinical Pharmacokinetics: Concepts and Applications. 3rd ed.Philadelphia, PA: Lippincott Williams & Wilkins; 1995.Google Scholar
West, GB, Brown, JH, Enquist, BJ. A general model for the origin of allometric scaling laws in biology. Science. 1997;276(5309):122–126.CrossRefGoogle ScholarPubMed
Mager, . Quantitative structure–pharmacokinetic/pharmacodynamic relationships. Adv Drug Deliv Rev. 2006;58(12–13):1326–1356.CrossRefGoogle ScholarPubMed
Wang, W, Wang, EQ, Balthasar, JP. Monoclonal antibody pharmacokinetics and pharmacodynamics. Clin Pharmacol Ther. 2008;84(5):548–558.CrossRefGoogle ScholarPubMed
Garg, A, Balthasar, J. Physiologically-based pharmacokinetic (PBPK) model to predict IgG tissue kinetics in wild-type and FcRn-knockout mice. J Pharmacokinet Pharmacodynam. 2007;34(5):687–709.CrossRefGoogle ScholarPubMed
Davda, JP, Jain, M, Batra, SK, Gwilt, PR, Robinson, DH. A physiologically based pharmacokinetic (PBPK) model to characterize and predict the disposition of monoclonal antibody CC49 and its single chain Fv constructs. Int Immunopharmacol. 2008;8(3):401–413.CrossRefGoogle ScholarPubMed
Lammerts van Bueren, JJ, Bleeker, WK, Bogh, HO, et al. Effect of target dynamics on pharmacokinetics of a novel therapeutic antibody against the epidermal growth factor receptor: Implications for the mechanisms of action. Cancer Res. 2006;66(15):7630–7638.CrossRefGoogle ScholarPubMed
Tabrizi, MA, Tseng, C-ML, Roskos, LK. Elimination mechanisms of therapeutic monoclonal antibodies. Drug Discov Today. 2006;11(1–2):81–88.CrossRefGoogle ScholarPubMed
Klee, EW, Carlson, DF, Fahrenkrug, SC, Ekker, SC, Ellis, LBM. Identifying secretomes in people, pufferfish and pigs. Nucleic Acids Res. 2004;32(4):1414–1421.CrossRefGoogle ScholarPubMed
Grimmond, SM, Miranda, KC, Yuan, Z, et al. The mouse secretome: Functional classification of the proteins secreted into the extracellular environment. Genome Res. 2003;13:1350–1359.CrossRefGoogle ScholarPubMed
Strachan, RT, Ferrara, G, Roth, BL. Screening the receptorome: An efficient approach for drug discovery and target validation. Drug Discov Today. 2006;11(15–16):708–716.CrossRefGoogle ScholarPubMed
Oda, K, Matsuoka, Y, Funahashi, A, Kitano, H. A comprehensive pathway map of epidermal growth factor receptor signaling. Mol Syst Biol. 2005;1–17.CrossRefGoogle ScholarPubMed
Hendriks, BS, Hua, F, Chabot, JR. Analysis of mechanistic pathway models in drug discovery: p38 pathway. Biotechnol Progr. 2008;24(1):96–109.CrossRefGoogle ScholarPubMed
Wiley, HS, Shvartsman, SY, Lauffenburger, DA. Computational modeling of the EGF-receptor system: A paradigm for systems biology. Trends Cell Biol. 2003;13(1): 43–50.CrossRefGoogle ScholarPubMed
Levenspiel, O. Chemical Reaction Engineering. 3rd ed.Hoboken, NJ: Wiley; 1998.Google Scholar
Deen, WM. Analysis of Transport Phenomena.New York, NY: Oxford University Press; 1998.Google Scholar
Dickman, S. Tough mining. Plos Biol. 2003;1(2):144.CrossRefGoogle ScholarPubMed
Roopenian, DC, FcRn, Akilesh S.: The neonatal Fc receptor comes of age. Nat Rev Immunol. 2007;7:715–725.CrossRefGoogle ScholarPubMed
JJLv, Bueren, Bleeker, WK, Bøgh, HO, et al. Effect of target dynamics on pharmacokinetics of a novel therapeutic antibody against the epidermal growth factor receptor: Implications for the mechanisms of action. Cancer Res. 2006;66:7630–7638.Google Scholar
Finkelman, FD, Madden, KB, Morris, SC, et al. Anti-cytokine antibodies as carrier proteins. Prolongation of in vivo effects of exogenous cytokines by injection of cytokine-anti-cytokine antibody complexes. J Immunol. 1993;151(3):1235–1244.Google ScholarPubMed
Lu, Z-Y, Brailly, H, Rossi, J-F, Wijdenes, J, Bataille, R, Klein, B. Overall interleukin-6 production exceeds 7 mg/day in multiple myeloma complicated by sepsis. Cytokine. 1993;5(6):578–582.CrossRefGoogle ScholarPubMed
Kishimoto, T. Interleukin-6: Discovery of a pleiotropic cytokine. Arthritis Res. Ther. 2006;8(Suppl 2):S2.CrossRefGoogle ScholarPubMed
Haringman, JJ, Gerlag, DM, Smeets, TJM, et al. A randomized controlled trial with an anti-CCL2 (anti-monocyte chemotactic protein 1) monoclonal antibody in patients with rheumatoid arthritis. Arthritis & Rheumatism. 2006;54(8):2387–2392.CrossRefGoogle ScholarPubMed
Jones, AT, Ziltener, HJ. Enhancement of the biologic effects of interleukin-3 in vivo by anti- interleukin-3 antibodies. Blood. 1993;82(4):1133–1141.Google ScholarPubMed
Mihara, M, Koishihara, Y, Fukui, H, Yasukawa, K, Ohsugi, Y. Murine anti-human IL-6 monoclonal antibody prolongs the half-life in circulating blood and thus prolongs the bioactivity of human IL-6 in mice. Immunology. 1991;74(1):55–59.Google ScholarPubMed
Slifka, MK, Whitton, JL. Clinical implications of dysregulated cytokine production. J Molec Med. 2000;78(2):74–80.CrossRefGoogle ScholarPubMed
Suzuki, H, Takemura, H, Yoshizaki, K, et al. IL-6-anti-IL-6 autoantibody complexes with IL-6 activity in sera from some patients with systemic sclerosis. J Immunol. 1994;152(2):935–942.Google ScholarPubMed
Ewer, SM, Ewer, MS. Cardiotoxicity profile of trastuzumab. Drug Saf. 2008;31(6): 459–467.CrossRefGoogle ScholarPubMed
Perez, EA. Cardiac toxicity of ErbB2-targeted therapies: what do we know?Clin Breast Cancer. 2008;8:S114-S120.CrossRefGoogle ScholarPubMed
Suter, TM, Cook-Brunsb, , Bartonc, C. Cardiotoxicity associated with trastuzumab (Herceptin) therapy in the treatment of metastatic breast cancer. The Breast. 2004;13(3):173–183.CrossRefGoogle ScholarPubMed
Kovtun, YV, Goldmacher, VS. Cell killing by antibody–drug conjugates. Cancer Lett. 2007;255(2):232–240.CrossRefGoogle ScholarPubMed
Schellekens, H. Immunogenicity of therapeutic proteins: Clinical implications and future prospects. Clin Therapeut. 2002;24(11):1720–1740.CrossRefGoogle ScholarPubMed
Pendley, C, Schantz, A, Wagner, C. Immunogenicity of therapeutic monoclonal antibodies. Curr Opin Molec Therapeut. 2003;5:172–179.Google ScholarPubMed
Kessler, M, Goldsmith, D, Schellekens, H. Immunogenicity of biopharmaceuticals. Nephrology Dialysis Transplantation. 2006;21:v9–v12.CrossRefGoogle ScholarPubMed
Schellekens, H. Bioequivalence and the immunogenicity of biopharmaceuticals. Nat Rev Drug Discov. 2002;1(6):457–462.CrossRefGoogle ScholarPubMed
Crommelin, DJA, Sindelar, RD, Meibohm, B, eds. Pharmaceutical Biotechnology: Fundamentals and Applications. 3rd ed.Philadelphia, PA: Informa HealthCare; 2007.CrossRef
Ghosh, S, Goldin, E, Gordon, FH, et al. Natalizumab for active Crohn's disease. N Engl J Med. 2003;348(1):24–32.CrossRefGoogle ScholarPubMed
Fineberg, SE, Galloway, JA, Fineberg, NS, Rathbun, MJ, Hufferd, S. Immunogenicity of recombinant DNA human insulin. Diabetologia. 1983;25(6):465–469.CrossRefGoogle ScholarPubMed
Perelson, AS. Modelling viral and immune system dynamics. Nat Rev Immunol. 2002;2(1):28–36.CrossRefGoogle ScholarPubMed
Chakraborty, AK, Dustin, ML, Shaw, AS. In silico models for cellular and molecular immunology: successes, promises and challenges. Nat Immunol. 2003;4(10):933–936.CrossRefGoogle Scholar
Goldstein, B, Faeder, JR, Hlavacek, WS. Mathematical and computational models of immune-receptor signalling. Nat Rev Immunol. 2004;4(6):445–456.CrossRefGoogle ScholarPubMed
Lenz, H-J. Management and preparedness for infusion and hypersensitivity reactions. The Oncologist. 2007;12(5):601–609.CrossRefGoogle ScholarPubMed
Mosekilde, E, Jensen, KS, Binder, C, Pramming, S, Thorsteinsson, B.Modeling absorption kinetics of subcutaneous injected soluble insulinJ Pharmacokinet Pharmacodynam. 1989;17(1):67–87.CrossRefGoogle ScholarPubMed
Wach, P, Trajanoski, Z, Kotanko, P, Skrabal, F. Numerical approximation of mathematical model for absorption of subcutaneously injected insulin. Med Biol Eng Comput. 1995;33(1):18–23.CrossRefGoogle ScholarPubMed
Muller, PY, Brennan, FR. Safety assessment and dose selection for first-in-human clinical trials with immunomodulatory monoclonal antibodies. Clin Pharmacol Ther. 2009;85(3):247–258.CrossRefGoogle ScholarPubMed
Suntharalingam, G, Perry, MR, Ward, S, et al. Cytokine storm in a phase 1 trial of the anti-CD28 monoclonal antibody TGN1412. N Engl J Med. 2006;355(10):1018–1028.CrossRefGoogle Scholar
Duff, GW. Expert Group on Phase One Clinical Trials.Norwich, UK: Department of Health (UK); 2006.Google Scholar

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