메뉴 건너뛰기




Volumn 37, Issue 2, 2016, Pages 66-74

Challenges and advances in the assessment of the disposition of antibody-drug conjugates

Author keywords

antibody drug conjugate; biotherapeutics; cancer; pharmacokinetics; preclinical

Indexed keywords

ANTIBODY CONJUGATE; CYTOTOXIC AGENT; DRUG ANTIBODY; ANTINEOPLASTIC AGENT; MONOCLONAL ANTIBODY;

EID: 84930607275     PISSN: 01422782     EISSN: 1099081X     Source Type: Journal    
DOI: 10.1002/bdd.1957     Document Type: Review
Times cited : (42)

References (43)
  • 1
    • 84873053339 scopus 로고    scopus 로고
    • Antibody-drug conjugates in cancer therapy
    • Sievers EL, Senter PD,. Antibody-drug conjugates in cancer therapy. Annu Rev Med 2013; 64: 15-29.
    • (2013) Annu Rev Med , vol.64 , pp. 15-29
    • Sievers, E.L.1    Senter, P.D.2
  • 2
    • 49449119098 scopus 로고    scopus 로고
    • Antibody-drug conjugates for cancer therapy
    • Carter PJ, Senter PD,. Antibody-drug conjugates for cancer therapy. Cancer J 2008; 14 (3): 154-169.
    • (2008) Cancer J , vol.14 , Issue.3 , pp. 154-169
    • Carter, P.J.1    Senter, P.D.2
  • 3
    • 84874343465 scopus 로고    scopus 로고
    • Drug-conjugated antibodies for the treatment of cancer
    • Lambert JM,. Drug-conjugated antibodies for the treatment of cancer. Br J Clin Pharmacol 2012; 76 (2): 248-262.
    • (2012) Br J Clin Pharmacol , vol.76 , Issue.2 , pp. 248-262
    • Lambert, J.M.1
  • 4
    • 84877310777 scopus 로고    scopus 로고
    • Maturing antibody-drug conjugate pipeline hits 30
    • Mullard A,. Maturing antibody-drug conjugate pipeline hits 30. Nature Rev Drug Discov 2013; 12: 329-332.
    • (2013) Nature Rev Drug Discov , vol.12 , pp. 329-332
    • Mullard, A.1
  • 6
    • 84866735537 scopus 로고    scopus 로고
    • Pharmacokinetic considerations for antibody drug conjugates
    • Lin K, Tibbitts J,. Pharmacokinetic considerations for antibody drug conjugates. Pharm Res 2012; 29: 2354-2366.
    • (2012) Pharm Res , vol.29 , pp. 2354-2366
    • Lin, K.1    Tibbitts, J.2
  • 7
    • 84869137056 scopus 로고    scopus 로고
    • ADME of antibody-maytansinoid conjugates
    • Erickson HK, Lambert JM,. ADME of antibody-maytansinoid conjugates. AAPS J 2012; 14 (4): 799-805.
    • (2012) AAPS J , vol.14 , Issue.4 , pp. 799-805
    • Erickson, H.K.1    Lambert, J.M.2
  • 8
    • 84871362496 scopus 로고    scopus 로고
    • Antibody-drug conjugates for the treatment of cancer
    • Flygare JA, Pillow TH, Aristoff P,. Antibody-drug conjugates for the treatment of cancer. Chem Biol Drug Des 2013; 81: 113-121.
    • (2013) Chem Biol Drug des , vol.81 , pp. 113-121
    • Flygare, J.A.1    Pillow, T.H.2    Aristoff, P.3
  • 9
    • 84862752215 scopus 로고    scopus 로고
    • The effect of different linkers on target cell catabolism and pharmacokinetics/pharmacodynamics of trastuzumab maytansinoid conjugates
    • Erickson HK, Lewis Phillips GD, Leipold DD, et al., The effect of different linkers on target cell catabolism and pharmacokinetics/pharmacodynamics of trastuzumab maytansinoid conjugates. Mol Cancer Ther 2012; 11 (5): 1133-1142.
    • (2012) Mol Cancer Ther , vol.11 , Issue.5 , pp. 1133-1142
    • Erickson, H.K.1    Lewis Phillips, G.D.2    Leipold, D.D.3
  • 10
    • 6044223544 scopus 로고    scopus 로고
    • Effects of drug loading on the antitumor activity of a monoclonal antibody drug conjugate
    • Hamblett KJ, Senter PD, Chace DF, et al., Effects of drug loading on the antitumor activity of a monoclonal antibody drug conjugate. Clin Cancer Res 2004; 10: 7063-7070.
    • (2004) Clin Cancer Res , vol.10 , pp. 7063-7070
    • Hamblett, K.J.1    Senter, P.D.2    Chace, D.F.3
  • 12
    • 84856120429 scopus 로고    scopus 로고
    • Monoclonal antibodies: What are the pharmacokinetic and pharmacodynamics considerations for drug development?
    • Deng R, Jin F, Prabhu S, Iyer S,. Monoclonal antibodies: what are the pharmacokinetic and pharmacodynamics considerations for drug development? Expert Opin Drug Metab Toxicol 2012; 8 (2): 141-160.
    • (2012) Expert Opin Drug Metab Toxicol , vol.8 , Issue.2 , pp. 141-160
    • Deng, R.1    Jin, F.2    Prabhu, S.3    Iyer, S.4
  • 13
    • 72949106918 scopus 로고    scopus 로고
    • Pharmacokinetics of biotech drugs: Peptides, proteins and monoclonal antibodies
    • Lin JH,. Pharmacokinetics of biotech drugs: peptides, proteins and monoclonal antibodies. Curr Drug Metabol 2009; 10: 661-691.
    • (2009) Curr Drug Metabol , vol.10 , pp. 661-691
    • Lin, J.H.1
  • 14
    • 84866736720 scopus 로고    scopus 로고
    • Anti-neuropilin-1 (MNRP1685A): Unexpected pharmacokinetic differences across species, from preclinical models to humans
    • Xin Y, Bai S, Damico-Beyer LA, et al., Anti-neuropilin-1 (MNRP1685A): unexpected pharmacokinetic differences across species, from preclinical models to humans. Pharm Res 2012; 29 (9): 2512-2521.
    • (2012) Pharm Res , vol.29 , Issue.9 , pp. 2512-2521
    • Xin, Y.1    Bai, S.2    Damico-Beyer, L.A.3
  • 15
    • 77951156788 scopus 로고    scopus 로고
    • Cross-species binding analyses of mouse and human neonatal Fc receptor show dramatic differences in immunoglobulin G and albumin binding
    • Andersen JT, Daba MB, Berntzen G, Michaelsen TE, Sandlie I,. Cross-species binding analyses of mouse and human neonatal Fc receptor show dramatic differences in immunoglobulin G and albumin binding. J Biol Chem 2010; 285: 4826-4836.
    • (2010) J Biol Chem , vol.285 , pp. 4826-4836
    • Andersen, J.T.1    Daba, M.B.2    Berntzen, G.3    Michaelsen, T.E.4    Sandlie, I.5
  • 16
    • 84899030660 scopus 로고    scopus 로고
    • Auristatin antibody drug conjugate physical instability and the role of drug payload
    • Adem YT1, Schwarz KA, Duenas E, Patapoff TW, Galush WJ, Esue O,. Auristatin antibody drug conjugate physical instability and the role of drug payload. Bioconjug Chem 2014; 25 (4): 656-664.
    • (2014) Bioconjug Chem , vol.25 , Issue.4 , pp. 656-664
    • Adem, Y.1    Schwarz, K.A.2    Duenas, E.3    Patapoff, T.W.4    Galush, W.J.5    Esue, O.6
  • 18
    • 84872957381 scopus 로고    scopus 로고
    • Bioanalytical assay strategies for the development of antibody-drug conjugate biotherapeutics
    • Kaur S, Xu K, Saad OM, Dere FC, Carrasco-Triguero M,. Bioanalytical assay strategies for the development of antibody-drug conjugate biotherapeutics. Bioanalysis 2013; 5 (2): 201-226.
    • (2013) Bioanalysis , vol.5 , Issue.2 , pp. 201-226
    • Kaur, S.1    Xu, K.2    Saad, O.M.3    Dere, F.C.4    Carrasco-Triguero, M.5
  • 19
    • 84877245142 scopus 로고    scopus 로고
    • Bioanalysis of antibody-drug conjugates: American Association of Pharmaceutical Scientists Antibody-Drug Conjugate Working Group position paper
    • Gorovits B, Alley SC, Bilic S, et al., Bioanalysis of antibody-drug conjugates: American Association of Pharmaceutical Scientists Antibody-Drug Conjugate Working Group position paper. Bioanalysis 2013; 5 (9): 997-1006.
    • (2013) Bioanalysis , vol.5 , Issue.9 , pp. 997-1006
    • Gorovits, B.1    Alley, S.C.2    Bilic, S.3
  • 20
    • 79952450423 scopus 로고    scopus 로고
    • Characterization of intact antibody-drug conjugates from plasma/serum in vivo by affinity capture capillary liquid chromatography-mass spectrometry
    • Xu K, Liu L, Saad OM, et al., Characterization of intact antibody-drug conjugates from plasma/serum in vivo by affinity capture capillary liquid chromatography-mass spectrometry. Anal Biochem 2011; 412: 56-66.
    • (2011) Anal Biochem , vol.412 , pp. 56-66
    • Xu, K.1    Liu, L.2    Saad, O.M.3
  • 21
    • 84877281414 scopus 로고    scopus 로고
    • Characterization of the drug-to-antibody ratio distribution for antibody-drug conjugates in plasma/serum
    • Xu K, Liu L, Dere R, et al., Characterization of the drug-to-antibody ratio distribution for antibody-drug conjugates in plasma/serum. Bioanalysis 2013; 5 (9): 1057-1071.
    • (2013) Bioanalysis , vol.5 , Issue.9 , pp. 1057-1071
    • Xu, K.1    Liu, L.2    Dere, R.3
  • 22
    • 84897474532 scopus 로고    scopus 로고
    • Measurement of in vivo drug load distribution of cysteine-linked antibody-drug conjugates using microscale liquid chromatography mass spectrometry
    • Hengel SM, Sanderson R, Valliere-Douglass J, Nicholas N, Leiske C, Alley SC,. Measurement of in vivo drug load distribution of cysteine-linked antibody-drug conjugates using microscale liquid chromatography mass spectrometry. Anal Chem 2014; 86 (7): 3420-3425.
    • (2014) Anal Chem , vol.86 , Issue.7 , pp. 3420-3425
    • Hengel, S.M.1    Sanderson, R.2    Valliere-Douglass, J.3    Nicholas, N.4    Leiske, C.5    Alley, S.C.6
  • 23
    • 84866170999 scopus 로고    scopus 로고
    • Differential effects of predosing on tumor and tissue uptake of an 111In-labeled anti-TENB2 antibody-drug conjugate
    • Boswell CA, Mundo EE, Zhang C, et al., Differential effects of predosing on tumor and tissue uptake of an 111In-labeled anti-TENB2 antibody-drug conjugate. J Nucl Med 2012; 53 (9): 1454-1461.
    • (2012) J Nucl Med , vol.53 , Issue.9 , pp. 1454-1461
    • Boswell, C.A.1    Mundo, E.E.2    Zhang, C.3
  • 24
    • 70349083423 scopus 로고    scopus 로고
    • The pharmacologic basis for antibody-auristatin conjugate activity
    • Alley SC, Zhang X, Okeley NM, et al., The pharmacologic basis for antibody-auristatin conjugate activity. J Pharmacol Exp Ther 2009; 330 (3): 932-938.
    • (2009) J Pharmacol Exp Ther , vol.330 , Issue.3 , pp. 932-938
    • Alley, S.C.1    Zhang, X.2    Okeley, N.M.3
  • 25
    • 80054794058 scopus 로고    scopus 로고
    • Impact of drug conjugation on pharmacokinetics and tissue distribution of anti-STEAP1 antibody-drug conjugates in rats
    • Boswell CA, Mundo EE, Zhang C, et al., Impact of drug conjugation on pharmacokinetics and tissue distribution of anti-STEAP1 antibody-drug conjugates in rats. Bioconjug Chem 2011; 22 (10): 1994-2004.
    • (2011) Bioconjug Chem , vol.22 , Issue.10 , pp. 1994-2004
    • Boswell, C.A.1    Mundo, E.E.2    Zhang, C.3
  • 26
    • 84862769765 scopus 로고    scopus 로고
    • Compartmental tissue distribution of antibody therapeutics: Experimental approaches and interpretations
    • Boswell CA, Bumbaca D, Fielder PJ, Khawli LA,. Compartmental tissue distribution of antibody therapeutics: experimental approaches and interpretations. AAPS J 2012; 14 (3): 612-618.
    • (2012) AAPS J , vol.14 , Issue.3 , pp. 612-618
    • Boswell, C.A.1    Bumbaca, D.2    Fielder, P.J.3    Khawli, L.A.4
  • 27
    • 70350712272 scopus 로고    scopus 로고
    • Phase I biodistribution and pharmacokinetic study of Lewis Y-targeting immunoconjugate CMD-193 in patients with advanced epithelial cancers
    • Herbertson RA, Tebbutt NC, Lee FT, et al., Phase I biodistribution and pharmacokinetic study of Lewis Y-targeting immunoconjugate CMD-193 in patients with advanced epithelial cancers. Clin Cancer Res 2009; 15 (21): 6709-6715.
    • (2009) Clin Cancer Res , vol.15 , Issue.21 , pp. 6709-6715
    • Herbertson, R.A.1    Tebbutt, N.C.2    Lee, F.T.3
  • 28
    • 84908356069 scopus 로고    scopus 로고
    • A mechanistic pharmacokinetic model elucidating the disposition of trastuzumab emtansine (T-DM1), an antibody-drug conjugate (ADC) for treatment of metastatic breast cancer
    • Bender B, Leipold DD, Xu K, Shen BQ, Tibbitts J, Friberg LE,. A mechanistic pharmacokinetic model elucidating the disposition of trastuzumab emtansine (T-DM1), an antibody-drug conjugate (ADC) for treatment of metastatic breast cancer. AAPS J 2014; 16 (5): 994-1008.
    • (2014) AAPS J , vol.16 , Issue.5 , pp. 994-1008
    • Bender, B.1    Leipold, D.D.2    Xu, K.3    Shen, B.Q.4    Tibbitts, J.5    Friberg, L.E.6
  • 29
    • 84907598646 scopus 로고    scopus 로고
    • Population pharmacokinetics of trastuzumab emtansine (T-DM1), a HER2-targeted antibody-drug conjugate, in patients with HER2-positive metastatic breast cancer: Clinical implications of the effect of covariates
    • Lu D, Girish S, Gao Y, et al., Population pharmacokinetics of trastuzumab emtansine (T-DM1), a HER2-targeted antibody-drug conjugate, in patients with HER2-positive metastatic breast cancer: clinical implications of the effect of covariates. Cancer Chemother Pharmacol 2014; 74 (2): 399-410.
    • (2014) Cancer Chemother Pharmacol , vol.74 , Issue.2 , pp. 399-410
    • Lu, D.1    Girish, S.2    Gao, Y.3
  • 30
    • 84895073197 scopus 로고    scopus 로고
    • Target-mediated drug disposition model and its approximations for antibody-drug conjugates
    • Gibiansky L, Gibiansky E,. Target-mediated drug disposition model and its approximations for antibody-drug conjugates. J Pharmacokinet Pharmacodyn 2014; 41 (1): 35-47.
    • (2014) J Pharmacokinet Pharmacodyn , vol.41 , Issue.1 , pp. 35-47
    • Gibiansky, L.1    Gibiansky, E.2
  • 31
    • 84880733804 scopus 로고    scopus 로고
    • Bench to bedside translation of antibody drug conjugates using a multiscale mechanistic PK/PD model: A case study with brentuximab-vedotin
    • Shah DK, Haddish-Berhane N, Betts A,. Bench to bedside translation of antibody drug conjugates using a multiscale mechanistic PK/PD model: a case study with brentuximab-vedotin. J Pharmacokinet Pharmacodyn 2012; 39 (6): 643-659.
    • (2012) J Pharmacokinet Pharmacodyn , vol.39 , Issue.6 , pp. 643-659
    • Shah, D.K.1    Haddish-Berhane, N.2    Betts, A.3
  • 32
    • 84903759033 scopus 로고    scopus 로고
    • Comparative clinical pharmacokinetics of antibody-drug conjugates in first-in-human Phase 1 studies
    • Deslandes A,. Comparative clinical pharmacokinetics of antibody-drug conjugates in first-in-human Phase 1 studies. MAbs 2014; 6 (4): 859-870.
    • (2014) MAbs , vol.6 , Issue.4 , pp. 859-870
    • Deslandes, A.1
  • 33
    • 84865706368 scopus 로고    scopus 로고
    • Catabolic fate and pharmacokinetic characterization of trastuzumab emtansine (T-DM1): An emphasis on preclinical and clinical catabolism
    • Shen BQ, Bumbaca D, Saad O, et al., Catabolic fate and pharmacokinetic characterization of trastuzumab emtansine (T-DM1): an emphasis on preclinical and clinical catabolism. Curr Drug Metab 2012; 13 (7): 901-910.
    • (2012) Curr Drug Metab , vol.13 , Issue.7 , pp. 901-910
    • Shen, B.Q.1    Bumbaca, D.2    Saad, O.3
  • 34
    • 84888201843 scopus 로고    scopus 로고
    • Preclinical safety profile of trastuzumab emtansine (T-DM1): Mechanism of action of its cytotoxic component retained with improved tolerability
    • Poon KA, Flagella K, Beyer J, et al., Preclinical safety profile of trastuzumab emtansine (T-DM1): mechanism of action of its cytotoxic component retained with improved tolerability. Toxicol Appl Pharmacol 2013; 273 (2): 298-313.
    • (2013) Toxicol Appl Pharmacol , vol.273 , Issue.2 , pp. 298-313
    • Poon, K.A.1    Flagella, K.2    Beyer, J.3
  • 35
    • 77954031486 scopus 로고    scopus 로고
    • Phase I study of trastuzumab-DM1, an HER2 antibody-drug conjugate, given every 3 weeks to patients with HER2-positive metastatic breast cancer
    • Krop IE, Beeram M, Modi S, et al., Phase I study of trastuzumab-DM1, an HER2 antibody-drug conjugate, given every 3 weeks to patients with HER2-positive metastatic breast cancer. J Clin Oncol 2010; 28 (16): 2698-2704.
    • (2010) J Clin Oncol , vol.28 , Issue.16 , pp. 2698-2704
    • Krop, I.E.1    Beeram, M.2    Modi, S.3
  • 36
    • 56449129810 scopus 로고    scopus 로고
    • Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate
    • Lewis Phillips GD, Li G, Dugger DL, et al., Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate. Cancer Res 2008; 68 (22): 9280-9290.
    • (2008) Cancer Res , vol.68 , Issue.22 , pp. 9280-9290
    • Lewis Phillips, G.D.1    Li, G.2    Dugger, D.L.3
  • 37
    • 79955042204 scopus 로고    scopus 로고
    • Design of antibody-maytansinoid conjugates allows for efficient detoxification via liver metabolism
    • Sun X, Widdison W, Mayo M, et al., Design of antibody-maytansinoid conjugates allows for efficient detoxification via liver metabolism. Bioconjug Chem 2011; 22 (4): 728-735.
    • (2011) Bioconjug Chem , vol.22 , Issue.4 , pp. 728-735
    • Sun, X.1    Widdison, W.2    Mayo, M.3
  • 38
    • 78049515807 scopus 로고    scopus 로고
    • Brentuximab vedotin (SGN-35) for relapsed CD30-positive lymphomas
    • Younes A, Bartlett NL, Leonard JP, et al., Brentuximab vedotin (SGN-35) for relapsed CD30-positive lymphomas. N Engl J Med 2010; 363 (19): 1812-1821.
    • (2010) N Engl J Med , vol.363 , Issue.19 , pp. 1812-1821
    • Younes, A.1    Bartlett, N.L.2    Leonard, J.P.3
  • 39
    • 84863012529 scopus 로고    scopus 로고
    • Conjugation site modulates the in vivo stability and therapeutic activity of antibody-drug conjugates
    • Shen BQ, Xu K, Liu L, et al., Conjugation site modulates the in vivo stability and therapeutic activity of antibody-drug conjugates. Nat Biotechnol 2012; 30: 184-189.
    • (2012) Nat Biotechnol , vol.30 , pp. 184-189
    • Shen, B.Q.1    Xu, K.2    Liu, L.3
  • 40
    • 84874300889 scopus 로고    scopus 로고
    • Location matters: Site of conjugation modulates stability and pharmacokinetics of antibody drug conjugates
    • Strop P1, Liu SH, Dorywalska M, et al., Location matters: site of conjugation modulates stability and pharmacokinetics of antibody drug conjugates. Chem Biol 2013; 20 (2): 161-167.
    • (2013) Chem Biol , vol.20 , Issue.2 , pp. 161-167
    • Strop, P.1    Liu, S.H.2    Dorywalska, M.3
  • 41
    • 84906043250 scopus 로고    scopus 로고
    • Antibody-drug conjugates: An emerging modality for the treatment of cancer
    • Leal M, Sapra P, Hurvitz SA, et al., Antibody-drug conjugates: an emerging modality for the treatment of cancer. Ann NY Acad Sci 2014; 1321 (1): 41-54.
    • (2014) Ann NY Acad Sci , vol.1321 , Issue.1 , pp. 41-54
    • Leal, M.1    Sapra, P.2    Hurvitz, S.A.3
  • 42
    • 0034770328 scopus 로고    scopus 로고
    • Pharmacokinetics of gemtuzumab ozogamicin, an antibody-targeted chemotherapy agent for the treatment of patients with acute myeloid leukemia in first relapse
    • Dowell JA, Korth-Bradley J, Liu H, King SP, Berger MS,. Pharmacokinetics of gemtuzumab ozogamicin, an antibody-targeted chemotherapy agent for the treatment of patients with acute myeloid leukemia in first relapse. J Clin Pharmacol 2001; 41: 1206-1214.
    • (2001) J Clin Pharmacol , vol.41 , pp. 1206-1214
    • Dowell, J.A.1    Korth-Bradley, J.2    Liu, H.3    King, S.P.4    Berger, M.S.5
  • 43
    • 84886825064 scopus 로고    scopus 로고
    • SGN-CD33A: A novel CD33-targeting antibody-drug conjugate using a pyrrolobenzodiazepine dimer is active in models of drug-resistant AML
    • Kung Sutherland MS, Walter RB, Jeffrey SC, et al., SGN-CD33A: a novel CD33-targeting antibody-drug conjugate using a pyrrolobenzodiazepine dimer is active in models of drug-resistant AML. Blood 2013; 122 (8): 1455-1463.
    • (2013) Blood , vol.122 , Issue.8 , pp. 1455-1463
    • Kung Sutherland, M.S.1    Walter, R.B.2    Jeffrey, S.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.