Therapeutic monoclonal antibody concentration monitoring: free or total?

Most therapeutic monoclonal antibodies are designed to bind a specific antigen to elicit pharmacological effects. Accurate quantification of a therapeutic monoclonal antibody in biological matrices is essential for assessing its pharmacokinetics and selecting an effective dosing regimen. Therapeutic antibodies may exist in free, partially bound and fully bound forms in the bloodstream. The choice of which form(s) to measure and how to measure them is gaining much attention with the increase in the number of soluble therapeutic targets. This article will review the bioanalytical methods used in supporting the clinical development of the US FDA-approved therapeutic monoclonal antibodies and also discuss how different factors, such as assay format, target and antibody concentrations, and sample dilutions, can have an impact on the measurement of each form of antibody. Appreciation of which form of drug is being measured and what factors may impact measurement under different conditions are important for interpretation of the pharmacokinetics of therapeutic antibodies.

[1]  J. S. Lee,et al.  Widely varying TNF-α levels in patients with myasthenia gravis , 2009, Neurological Sciences.

[2]  R H Levy,et al.  Rationale for Monitoring Free Drug Levels , 1984, Clinical pharmacokinetics.

[3]  J. Oh,et al.  Detection of epidermal growth factor receptor in the serum of gastric carcinoma patients , 1997, Cancer.

[4]  J. Arribas,et al.  Protein ectodomain shedding. , 2002, Chemical reviews.

[5]  G. Ciancio,et al.  Anti-interleukin-2 receptor antibodies-basiliximab and daclizumab-for the prevention of acute rejection in renal transplantation , 2009 .

[6]  Suzanne F. Jones,et al.  A Phase 1 Escalating Single-Dose and Weekly Fixed-Dose Study of Cetuximab: Pharmacokinetic and Pharmacodynamic Rationale for Dosing , 2007, Clinical Cancer Research.

[7]  L. Norton,et al.  Phase I studies of anti-epidermal growth factor receptor chimeric antibody C225 alone and in combination with cisplatin. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[8]  B. Meibohm,et al.  Pharmacokinetic aspects of biotechnology products. , 2004, Journal of pharmaceutical sciences.

[9]  R. Figlin,et al.  Safety, pharmacokinetics, and activity of ABX-EGF, a fully human anti-epidermal growth factor receptor monoclonal antibody in patients with metastatic renal cell cancer. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[10]  P. Kuebler,et al.  An Overview of the Pharmacokinetics and Pharmacodynamics of Efalizumab: A Monoclonal Antibody Approved for Use in Psoriasis , 2006, Journal of clinical pharmacology.

[11]  M. Berger,et al.  Pharmacokinetics of Gemtuzumab Ozogamicin, an Antibody‐Targeted Chemotherapy Agent for the Treatment of Patients with Acute Myeloid Leukemia in First Relapse , 2001, Journal of clinical pharmacology.

[12]  M. Koller,et al.  A safety and pharmacokinetic study of intravenous natalizumab in patients with MS , 1999, Neurology.

[13]  P. Beer,et al.  VITREOUS LEVELS OF UNBOUND BEVACIZUMAB AND UNBOUND VASCULAR ENDOTHELIAL GROWTH FACTOR IN TWO PATIENTS , 2006, Retina.

[14]  G. Meno-Tetang,et al.  On the prediction of the human response: a recycled mechanistic pharmacokinetic/pharmacodynamic approach. , 2005, Basic & clinical pharmacology & toxicology.

[15]  Daniel H. S. Silverman,et al.  Phase I/II 90Y-Zevalin (yttrium-90 ibritumomab tiuxetan, IDEC-Y2B8) radioimmunotherapy dosimetry results in relapsed or refractory non-Hodgkin’s lymphoma , 2000, European Journal of Nuclear Medicine.

[16]  L. Rassenti,et al.  Free circulating soluble CD52 as a tumor marker in chronic lymphocytic leukemia and its implication in therapy with anti‐CD52 antibodies , 2004, Cancer.

[17]  Rene Bruno,et al.  Clinical pharmacokinetics of bevacizumab in patients with solid tumors , 2008, Cancer Chemotherapy and Pharmacology.

[18]  G. Paintaud,et al.  Pharmacokinetics of rituximab and its clinical use: thought for the best use? , 2007, Critical reviews in oncology/hematology.

[19]  Y. Tsukamoto,et al.  A mechanism-based binding model for the population pharmacokinetics and pharmacodynamics of omalizumab. , 2007, British journal of clinical pharmacology.

[20]  B. Dijkmans,et al.  Relationship between serum trough infliximab levels, pretreatment C reactive protein levels, and clinical response to infliximab treatment in patients with rheumatoid arthritis , 2004, Annals of the rheumatic diseases.

[21]  F. Appelbaum,et al.  Monoclonal antibody 1F5 (anti-CD20) serotherapy of human B cell lymphomas. , 1987, Blood.

[22]  L. Goodman,et al.  The Pharmacological Basis of Therapeutics , 1941 .

[23]  G. Sledge,et al.  Phase I safety and pharmacokinetic study of recombinant human anti-vascular endothelial growth factor in patients with advanced cancer. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[24]  J. Fox,et al.  Tissue distribution and complex formation with IgE of an anti-IgE antibody after intravenous administration in cynomolgus monkeys. , 1996, The Journal of pharmacology and experimental therapeutics.

[25]  J. Pulido,et al.  Pharmacokinetics of intravitreal bevacizumab (Avastin). , 2007, Ophthalmology.

[26]  Wei-Ching Liang,et al.  Technology comparisons for anti-therapeutic antibody and neutralizing antibody assays in the context of an anti-TNF pharmacokinetic study. , 2009, Journal of immunological methods.

[27]  R. Slavin,et al.  Asthma symptom re-emergence after omalizumab withdrawal correlates well with increasing IgE and decreasing pharmacokinetic concentrations. , 2009, The Journal of allergy and clinical immunology.

[28]  A. Balcerska,et al.  Serum soluble interleukin 2 receptor α in human cancer of adults and children: a review , 2008 .

[29]  E. Kubista,et al.  Serum EGFR levels and efficacy of trastuzumab-based therapy in patients with metastatic breast cancer. , 2006, European journal of cancer.

[30]  L. Steinman,et al.  Administration of Neutralizing Antibodies to Interleukin-6 (IL-6) Reduces Experimental Autoimmune Encephalomyelitis and Is Associated with Elevated Levels of IL-6 Bioactivity in Central Nervous System and Circulation , 1995, Molecular medicine.

[31]  R. Eckert,et al.  In Vitro Internalization, Intracellular Transport, and Clearance of an Anti-CD11a Antibody (Raptiva) by Human T-Cells , 2004, Journal of Pharmacology and Experimental Therapeutics.

[32]  I. Pastan,et al.  High Shed Antigen Levels within Tumors: An Additional Barrier to Immunoconjugate Therapy , 2008, Clinical Cancer Research.

[33]  G. Hale,et al.  Pharmacokinetics of CAMPATH-1H: assay development and validation. , 2002, Journal of immunological methods.

[34]  T. Illidge,et al.  A new anti-idiotype antibody capable of binding rituximab on the surface of lymphoma cells. , 2004, Blood.

[35]  L. Steinman Blocking adhesion molecules as therapy for multiple sclerosis: natalizumab , 2005, Nature Reviews Drug Discovery.

[36]  I Royston,et al.  IDEC-C2B8 (Rituximab) anti-CD20 monoclonal antibody therapy in patients with relapsed low-grade non-Hodgkin's lymphoma. , 1997, Blood.

[37]  A. Nagler,et al.  Soluble interleukin-2 receptor levels in cytomegalovirus disease and graft versus host disease after T-lymphocyte depleted bone marrow transplantation for hematological neoplasias. , 1994, Leukemia & lymphoma.

[38]  K. Do,et al.  Circulating CD20 is detectable in the plasma of patients with chronic lymphocytic leukemia and is of prognostic significance. , 2003, Blood.

[39]  F. Breedveld,et al.  Regulation of cytokines, cytokine inhibitors, and acute-phase proteins following anti-TNF-alpha therapy in rheumatoid arthritis. , 1999, Journal of immunology.

[40]  D. Marmé,et al.  Vascular endothelial growth factor in the sera and effusions of patients with malignant and nonmalignant disease , 1999, Cancer.

[41]  D. S. Riggs,et al.  Thyroid function in nephrosis. , 1952, The Journal of clinical investigation.

[42]  R. Tacey,et al.  Development and validation of ELISA for herceptin detection in human serum. , 2004, Journal of immunological methods.

[43]  Helen J. Lachmann,et al.  In vivo regulation of interleukin 1β in patients with cryopyrin-associated periodic syndromes , 2009, The Journal of experimental medicine.

[44]  P. Hawkins,et al.  Use of canakinumab in the cryopyrin-associated periodic syndrome. , 2009, The New England journal of medicine.

[45]  W Wang,et al.  Monoclonal Antibody Pharmacokinetics and Pharmacodynamics , 2008, Clinical pharmacology and therapeutics.

[46]  C. Maury,et al.  Radioimmunoassay of tumor necrosis factor in serum. , 1987, Clinical chemistry.

[47]  M. Blumenthal,et al.  Robustness into advanced age of atopy-specific mechanisms in atopy-prone families. , 2003, The journals of gerontology. Series A, Biological sciences and medical sciences.

[48]  J. Grandis,et al.  Pharmacokinetic and pharmacodynamic properties of EGFR inhibitors under clinical investigation. , 2004, Cancer treatment reviews.

[49]  D. Norman Mechanisms of Action and Overview of OKT3 , 1995, Therapeutic drug monitoring.

[50]  M. Maurel,et al.  Evaluation of a peptide ELISA for the detection of rituximab in serum. , 2007, Journal of immunological methods.

[51]  J. Schölmerich,et al.  Inadequately low serum levels of steroid hormones in relation to interleukin-6 and tumor necrosis factor in untreated patients with early rheumatoid arthritis and reactive arthritis. , 2002, Arthritis and rheumatism.

[52]  L. Matis,et al.  Inhibition of complement activity by humanized anti-C5 antibody and single-chain Fv. , 1996, Molecular immunology.

[53]  N. Hogg,et al.  Shedding of lymphocyte function-associated antigen-1 (LFA-1) in a human inflammatory response. , 2006, Blood.

[54]  S. A. Bush,et al.  A phase I/II trial of iodine-131-tositumomab (anti-CD20), etoposide, cyclophosphamide, and autologous stem cell transplantation for relapsed B-cell lymphomas. , 2000, Blood.

[55]  I. T. Ten Berge,et al.  Pharmacokinetics of murine anti-human CD3 antibodies in man are determined by the disappearance of target antigen. , 2002, The Journal of pharmacology and experimental therapeutics.

[56]  Stanley B. Cohen,et al.  Pharmacokinetics and Safety of Golimumab, a Fully Human Anti‐TNF‐α Monoclonal Antibody, in Subjects With Rheumatoid Arthritis , 2007, Journal of clinical pharmacology.

[57]  D. Mould,et al.  Determination of humanized anti-Tac in human serum by a sandwich enzyme linked immunosorbent assay. , 1995, Journal of immunological methods.

[58]  J. Pulido,et al.  SIX-MONTH STABILITY OF BEVACIZUMAB (AVASTIN) BINDING TO VASCULAR ENDOTHELIAL GROWTH FACTOR AFTER WITHDRAWAL INTO A SYRINGE AND REFRIGERATION OR FREEZING , 2006, Retina.

[59]  L. Joosten,et al.  Effects of treatment with a fully human anti-tumour necrosis factor α monoclonal antibody on the local and systemic homeostasis of interleukin 1 and TNFα in patients with rheumatoid arthritis , 2001, Annals of the rheumatic diseases.

[60]  Janice M Reichert,et al.  Monoclonal antibodies as innovative therapeutics. , 2008, Current pharmaceutical biotechnology.

[61]  J. Baselga,et al.  Utility of serum HER2 extracellular domain assessment in clinical decision making: pooled analysis of four trials of trastuzumab in metastatic breast cancer. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[62]  P. Tak,et al.  Clinical response, pharmacokinetics, development of human anti-chimaeric antibodies, and synovial tissue response to rituximab treatment in patients with rheumatoid arthritis , 2009, Annals of the rheumatic diseases.

[63]  S. Richards,et al.  Effect of eculizumab on hemolysis and transfusion requirements in patients with paroxysmal nocturnal hemoglobinuria. , 2004, The New England journal of medicine.

[64]  N. Damle Tumour-targeted chemotherapy with immunoconjugates of calicheamicin , 2004, Expert opinion on biological therapy.

[65]  D Tripathy,et al.  Phase II study of receptor-enhanced chemosensitivity using recombinant humanized anti-p185HER2/neu monoclonal antibody plus cisplatin in patients with HER2/neu-overexpressing metastatic breast cancer refractory to chemotherapy treatment. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[66]  R. Ariagno,et al.  Safety, tolerance and pharmacokinetics of a humanized monoclonal antibody to respiratory syncytial virus in premature infants and infants with bronchopulmonary dysplasia. MEDI-493 Study Group. , 1998, The Pediatric infectious disease journal.

[67]  Eleftherios P. Diamandis,et al.  3 – THEORY OF IMMUNOASSAYS , 1996 .

[68]  G. Paintaud,et al.  An Enzyme-Linked Immunosorbent Assay for Therapeutic Drug Monitoring of Cetuximab , 2009, Therapeutic drug monitoring.

[69]  M. Tabrizi,et al.  Elimination mechanisms of therapeutic monoclonal antibodies. , 2006, Drug discovery today.

[70]  R. Hamilton,et al.  Immunological methods for quantifying free and total serum IgE levels in allergy patients receiving omalizumab (Xolair) therapy. , 2005, Journal of immunological methods.

[71]  Y. Sasaki,et al.  Dose escalation and pharmacokinetic study of a humanized anti-HER2 monoclonal antibody in patients with HER2/neu-overexpressing metastatic breast cancer , 1999, British Journal of Cancer.

[72]  H. Booker,et al.  Serum Concentrations of Free Diphenylhydantoin and their Relationship To Clinical Intoxication , 1973, Epilepsia.

[73]  N. Rawal,et al.  C5 Convertase of the Alternative Pathway of Complement , 1998, The Journal of Biological Chemistry.

[74]  A. Kennedy,et al.  Three new assays for rituximab based on its immunological activity or antigenic properties: analyses of sera and plasmas of RTX-treated patients with chronic lymphocytic leukemia and other B cell lymphomas. , 2004, Journal of immunological methods.

[75]  S. Tannenbaum,et al.  Relationship between omalizumab pharmacokinetics, IgE pharmacodynamics and symptoms in patients with severe persistent allergic (IgE-mediated) asthma. , 2009, British journal of clinical pharmacology.

[76]  D Tripathy,et al.  Phase II study of weekly intravenous recombinant humanized anti-p185HER2 monoclonal antibody in patients with HER2/neu-overexpressing metastatic breast cancer. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[77]  H. Paulus,et al.  Efficacy, pharmacokinetic, and safety assessment of adalimumab, a fully human anti-tumor necrosis factor-alpha monoclonal antibody, in adults with rheumatoid arthritis receiving concomitant methotrexate: a pilot study. , 2003, Clinical therapeutics.

[78]  R. Hansen,et al.  Antibody pharmacokinetics and pharmacodynamics. , 2004, Journal of pharmaceutical sciences.

[79]  R. Dockhorn,et al.  Use of an anti-IgE humanized monoclonal antibody in ragweed-induced allergic rhinitis. , 1997, The Journal of allergy and clinical immunology.

[80]  E. Raymond,et al.  Pharmacokinetic profile of cetuximab (Erbitux) alone and in combination with irinotecan in patients with advanced EGFR-positive adenocarcinoma. , 2005, European journal of cancer.

[81]  J. Armitage,et al.  Circulating CD20 and CD52 in patients with non‐Hodgkin's lymphoma or Hodgkin's disease , 2003, British journal of haematology.

[82]  B. Meibohm,et al.  Population Pharmacokinetics of Cetuximab in Patients With Squamous Cell Carcinoma of the Head and Neck , 2008, Journal of clinical pharmacology.

[83]  N. Casadevall,et al.  The immunophenotype of 177 adults with acute myeloid leukemia: proposal of a prognostic score. , 2000, Blood.

[84]  J. E. Rall,et al.  The interaction of thyroid hormones and protein in biological fluids. , 1957, Recent progress in hormone research.

[85]  H. Kantarjian,et al.  Alemtuzumab: validation of a sensitive and simple enzyme-linked immunosorbent assay. , 2004, Leukemia research.