-
1
-
-
77954031486
-
Phase I study of trastuzumab-DM1, a HER2 antibody-drug conjugate, given every 3 weeks to patients with HER2-positive metastatic breast cancer
-
Krop IE, Beeram M, Modi S, Jones SF, Holden SN, Yu W, Girish S, Tibbitts J, Yi JH, Sliwkowski MX, Jacobson F, Lutzker SG, Burris HA (2010) Phase I study of trastuzumab-DM1, a HER2 antibody-drug conjugate, given every 3 weeks to patients with HER2-positive metastatic breast cancer. J Clin Oncol 28:2698-2704
-
(2010)
J Clin Oncol
, vol.28
, pp. 2698-2704
-
-
Krop, I.E.1
Beeram, M.2
Modi, S.3
Jones, S.F.4
Holden, S.N.5
Yu, W.6
Girish, S.7
Tibbitts, J.8
Yi, J.H.9
Sliwkowski, M.X.10
Jacobson, F.11
Lutzker, S.G.12
Burris, H.A.13
-
2
-
-
78049515807
-
Brentuximab vedotin (SGN-35) for relapsed CD30-positive lymphomas
-
Younes A, Bartlett NL, Leonard JP, Kennedy DA, Lynch CM, Sievers EL, Forero-Torres A (2010) Brentuximab vedotin (SGN-35) for relapsed CD30-positive lymphomas. N Engl J Med 363:1812-1821
-
(2010)
N Engl J Med
, vol.363
, pp. 1812-1821
-
-
Younes, A.1
Bartlett, N.L.2
Leonard, J.P.3
Kennedy, D.A.4
Lynch, C.M.5
Sievers, E.L.6
Forero-Torres, A.7
-
3
-
-
79952092706
-
Phase II study of the antibody drug conjugate trastuzumab-DM1 for the treatment of human epidermal growth factor receptor 2 (HER2) - positive breast cancer after prior HER2-directed therapy
-
Burris HA III, Rugo HS, Vukelja SJ, Vogel CL, Borson RA, Limentani S, Tan-Chiu E, Krop IE, Michaelson RA, Girish S, Amler L, Zheng M, Chu YW, Klencke B, O'Shaughnessy JA (2011) Phase II study of the antibody drug conjugate trastuzumab-DM1 for the treatment of human epidermal growth factor receptor 2 (HER2) - positive breast cancer after prior HER2-directed therapy. J Clin Oncol 29:398-405
-
(2011)
J Clin Oncol
, vol.29
, pp. 398-405
-
-
Burris, H.A.1
Rugo, H.S.2
Vukelja, S.J.3
Vogel, C.L.4
Borson, R.A.5
Limentani, S.6
Tan-Chiu, E.7
Krop, I.E.8
Michaelson, R.A.9
Girish, S.10
Amler, L.11
Zheng, M.12
Chu, Y.W.13
Klencke, B.14
O'Shaughnessy, J.A.15
-
4
-
-
67649886201
-
Potent antibody drug conjugates for cancer therapy
-
Senter PD (2009) Potent antibody drug conjugates for cancer therapy. Curr Opin Chem Biol 13:235-244
-
(2009)
Curr Opin Chem Biol
, vol.13
, pp. 235-244
-
-
Senter, P.D.1
-
5
-
-
79959700509
-
Trastuzumab-DM1 (T-DM1) retains all the mechanisms of action of trastuzumab and efficiently inhibits growth of lapatinib insensitive breast cancer
-
Junttila TT, Li G, Parsons K, Lewis Phillips G, Sliwkowski MX (2011) Trastuzumab-DM1 (T-DM1) retains all the mechanisms of action of trastuzumab and efficiently inhibits growth of lapatinib insensitive breast cancer. Breast Cancer Res Treat 128:347-356
-
(2011)
Breast Cancer Res Treat
, vol.128
, pp. 347-356
-
-
Junttila, T.T.1
Li, G.2
Parsons, K.3
Lewis Phillips, G.4
Sliwkowski, M.X.5
-
6
-
-
33645500289
-
Anti-body-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker-dependent intracellular processing
-
Erickson HK, Park PU, Widdison WC, Kovtun YV, Garrett LM, Hoffman K, Lutz RJ, Goldmacher VS, Blättler WA (2006) Anti-body-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker-dependent intracellular processing. Cancer Res 66:4426-4433
-
(2006)
Cancer Res
, vol.66
, pp. 4426-4433
-
-
Erickson, H.K.1
Park, P.U.2
Widdison, W.C.3
Kovtun, Y.V.4
Garrett, L.M.5
Hoffman, K.6
Lutz, R.J.7
Goldmacher, V.S.8
Blättler, W.A.9
-
7
-
-
74949139946
-
Tumor delivery and in vivo processing of disulfide-linked and thioether-linked antibody-maytansinoid conjugates
-
Erickson HK, Widdison WC, Mayo MF, Whiteman K, Audette C, Wilhelm SD, Singh R (2010) Tumor delivery and in vivo processing of disulfide-linked and thioether-linked antibody-maytansinoid conjugates. Bioconjug Chem 21:84-92
-
(2010)
Bioconjug Chem
, vol.21
, pp. 84-92
-
-
Erickson, H.K.1
Widdison, W.C.2
Mayo, M.F.3
Whiteman, K.4
Audette, C.5
Wilhelm, S.D.6
Singh, R.7
-
8
-
-
84862752215
-
The effect of different linkers on target cell catabolism and pharmacokinetics/pharmacodynamics of trastuzumab maytansinoid conjugates
-
Erickson HK, Lewis-Phillips GD, Leipold DD, Provenzano CA, Mai E, Johnson HA, Gunter B, Audette CA, Gupta M, Pinkas J, Tibbitts J (2012) The effect of different linkers on target cell catabolism and pharmacokinetics/pharmacodynamics of trastuzumab maytansinoid conjugates. Mol Cancer Ther 11:1133-1142
-
(2012)
Mol Cancer Ther
, vol.11
, pp. 1133-1142
-
-
Erickson, H.K.1
Lewis-Phillips, G.D.2
Leipold, D.D.3
Provenzano, C.A.4
Mai, E.5
Johnson, H.A.6
Gunter, B.7
Audette, C.A.8
Gupta, M.9
Pinkas, J.10
Tibbitts, J.11
-
9
-
-
70349083423
-
The pharmacologic basis for antibody-auristatin conjugate activity
-
Alley SC, Zhang X, Okeley NM, Anderson M, Law CL, Senter PD, Benjamin DR (2009) The pharmacologic basis for antibody-auristatin conjugate activity. J Pharmacol Exp Ther 330:932-938
-
(2009)
J Pharmacol Exp Ther
, vol.330
, pp. 932-938
-
-
Alley, S.C.1
Zhang, X.2
Okeley, N.M.3
Anderson, M.4
Law, C.L.5
Senter, P.D.6
Benjamin, D.R.7
-
10
-
-
76049122850
-
Intracellular activation of SGN-35, a potent anti-CD30 antibody-drug conjugate
-
Okeley NM, Miyamoto JB, Zhang X, Sanderson RJ, Benjamin DR, Sievers EL, Senter PD, Alley SC (2010) Intracellular activation of SGN-35, a potent anti-CD30 antibody-drug conjugate. Clin Cancer Res 16:888-897
-
(2010)
Clin Cancer Res
, vol.16
, pp. 888-897
-
-
Okeley, N.M.1
Miyamoto, J.B.2
Zhang, X.3
Sanderson, R.J.4
Benjamin, D.R.5
Sievers, E.L.6
Senter, P.D.7
Alley, S.C.8
-
11
-
-
31544441685
-
Enhanced activity of monomethylauristatin F through monoclonal antibody delivery: Effects of linker technology on efficacy and toxicity
-
Doronina SO, Mendelsohn BA, Bovee TD, Cerveny CG, Alley SC, Meyer DL, Oflazoglu E, Toki BE, Sanderson RJ, Zabinski RF, Wahl AF, Senter PD (2006) Enhanced activity of monomethylauristatin F through monoclonal antibody delivery: effects of linker technology on efficacy and toxicity. Bioconjug Chem 17:114-124
-
(2006)
Bioconjug Chem
, vol.17
, pp. 114-124
-
-
Doronina, S.O.1
Mendelsohn, B.A.2
Bovee, T.D.3
Cerveny, C.G.4
Alley, S.C.5
Meyer, D.L.6
Oflazoglu, E.7
Toki, B.E.8
Sanderson, R.J.9
Zabinski, R.F.10
Wahl, A.F.11
Senter, P.D.12
-
12
-
-
0033730929
-
Pharmacokinetic/pharmacodynamic modeling in drug research and development
-
Derendorf H, Lesko LJ, Chaikin P, Colburn WA, Lee P, Miller R, Powell R, Rhodes G, Stanski D, Venitz J (2000) Pharmacokinetic/pharmacodynamic modeling in drug research and development. J Clin Pharmacol 40:1399-1418
-
(2000)
J Clin Pharmacol
, vol.40
, pp. 1399-1418
-
-
Derendorf, H.1
Lesko, L.J.2
Chaikin, P.3
Colburn, W.A.4
Lee, P.5
Miller, R.6
Powell, R.7
Rhodes, G.8
Stanski, D.9
Venitz, J.10
-
13
-
-
41349119550
-
Mechanism-based pharmacokinetic-pharmacodynamic (PK/PD) modeling in translational drug research
-
Danhof M, de Lange EC, Della Pasqua OE, Ploeger BA, Voskuyl RA (2008) Mechanism-based pharmacokinetic-pharmacodynamic (PK/PD) modeling in translational drug research. Trends Pharmacol Sci 29:186-191
-
(2008)
Trends Pharmacol Sci
, vol.29
, pp. 186-191
-
-
Danhof, M.1
De Lange, E.C.2
Della Pasqua, O.E.3
Ploeger, B.A.4
Voskuyl, R.A.5
-
14
-
-
0033667166
-
Models of schedule dependent hematological toxicity 2′-deoxy-2′-methylidinecytidine (DMDC)
-
Friberg LE, Brindley CJ, Karlsson MO, Devlin AJ (2000) Models of schedule dependent hematological toxicity 2′-deoxy-2′-methylidinecytidine (DMDC). Eur J Clin Pharmacol 56:567-574
-
(2000)
Eur J Clin Pharmacol
, vol.56
, pp. 567-574
-
-
Friberg, L.E.1
Brindley, C.J.2
Karlsson, M.O.3
Devlin, A.J.4
-
15
-
-
46449090520
-
Pharmacokinetic-pharmacodynamic modeling of biomarker response and tumor growth inhibition to an orally available cMet kinase inhibitor in human tumor xenograft mouse models
-
Yamazaki S, Skaptason J, Romero D, Lee JH, Zou HY, Christensen JG, Koup JR, Smith BJ, Koudriakova T (2008) Pharmacokinetic-pharmacodynamic modeling of biomarker response and tumor growth inhibition to an orally available cMet kinase inhibitor in human tumor xenograft mouse models. Drug Metab Dispos 36:1267-1274
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 1267-1274
-
-
Yamazaki, S.1
Skaptason, J.2
Romero, D.3
Lee, J.H.4
Zou, H.Y.5
Christensen, J.G.6
Koup, J.R.7
Smith, B.J.8
Koudriakova, T.9
-
16
-
-
67649344800
-
Demonstration of the equivalent pharmacokinetic/pharmacodynamic dosing strategy in a multiple-dose strategy of gefitinib
-
Wang S, Zhou Q, Gallo JM (2009) Demonstration of the equivalent pharmacokinetic/pharmacodynamic dosing strategy in a multiple-dose strategy of gefitinib. Mol Cancer Ther 8:1438-1447
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 1438-1447
-
-
Wang, S.1
Zhou, Q.2
Gallo, J.M.3
-
17
-
-
56449129810
-
Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate
-
Lewis Phillips GD, Li G, Dugger DL, Crocker LM, Parsons KL, Mai E, Blättler WA, Lambert JM, Chari RVJ, Lutz RJ, Wong WLT, Jacobson FS, Koeppen H, Schwall RH, Kenkare-Mitra SR, Spencer SD, Sliwkowski MX (2008) Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate. Cancer Res 68:9280-9290
-
(2008)
Cancer Res
, vol.68
, pp. 9280-9290
-
-
Lewis Phillips, G.D.1
Li, G.2
Dugger, D.L.3
Crocker, L.M.4
Parsons, K.L.5
Mai, E.6
Blättler, W.A.7
Lambert, J.M.8
Chari, R.V.J.9
Lutz, R.J.10
Wong, W.L.T.11
Jacobson, F.S.12
Koeppen, H.13
Schwall, R.H.14
Kenkare-Mitra, S.R.15
Spencer, S.D.16
Sliwkowski, M.X.17
-
18
-
-
84865706368
-
Catabolic fate and pharmacokinetic characterization of Trastuzumab emtansine (T-DM1): An emphasis on preclinical and clinical catabolism
-
Shen B-Q, Bumbaca D, Saad O, Yue Q, Pastuskovas CV, Khojasteh SC, Tibbitts J, Kaur S, Wang B, Chu Y-W, LoRusso PM, Girish S (2012) Catabolic fate and pharmacokinetic characterization of Trastuzumab emtansine (T-DM1): an emphasis on preclinical and clinical catabolism. Curr Drug Metab 13:901-910
-
(2012)
Curr Drug Metab
, vol.13
, pp. 901-910
-
-
Shen, B.-Q.1
Bumbaca, D.2
Saad, O.3
Yue, Q.4
Pastuskovas, C.V.5
Khojasteh, S.C.6
Tibbitts, J.7
Kaur, S.8
Wang, B.9
Chu, Y.-W.10
LoRusso, P.M.11
Girish, S.12
-
19
-
-
77956759089
-
Modeling the efficacy of trastuzumab-DM1, an antibody drug conjugate, in mice
-
Jumbe NL, Yan X, Leipold DD, Crocker L, Dugger D, Mai E, Sliwkowski MX, Fielder PJ, Tibbitts J (2010) Modeling the efficacy of trastuzumab-DM1, an antibody drug conjugate, in mice. J Pharmacokinet Pharmacodyn 37:221-242
-
(2010)
J Pharmacokinet Pharmacodyn
, vol.37
, pp. 221-242
-
-
Jumbe, N.L.1
Yan, X.2
Leipold, D.D.3
Crocker, L.4
Dugger, D.5
Mai, E.6
Sliwkowski, M.X.7
Fielder, P.J.8
Tibbitts, J.9
-
20
-
-
0842282616
-
Predictive pharmacokinetic-pharmacodynamic modeling of tumor growth kinetics in xenograft models after administration of anticancer agents
-
Simeoni M, Magni P, Cammia C, De Nicolao G, Croci V, Pesenti E, Germani M, Poggesi I, Rocchetti M (2004) Predictive pharmacokinetic-pharmacodynamic modeling of tumor growth kinetics in xenograft models after administration of anticancer agents. Cancer Res 64:1094-1101
-
(2004)
Cancer Res
, vol.64
, pp. 1094-1101
-
-
Simeoni, M.1
Magni, P.2
Cammia, C.3
De Nicolao, G.4
Croci, V.5
Pesenti, E.6
Germani, M.7
Poggesi, I.8
Rocchetti, M.9
-
22
-
-
9444252957
-
Endocytosis and sorting of ErbB2 and the site of action of cancer therapeutics trastuzumab and geldanamycin
-
Austin CD, De Maziere AM, Pisacane PI, van Dijk SM, Eigenbrot C, Sliwkowski MX, Klumperman J, Scheller RH (2004) Endocytosis and sorting of ErbB2 and the site of action of cancer therapeutics trastuzumab and geldanamycin. Molec Biol Cell 15:5268-5282
-
(2004)
Molec Biol Cell
, vol.15
, pp. 5268-5282
-
-
Austin, C.D.1
De Maziere, A.M.2
Pisacane, P.I.3
Van Dijk, S.M.4
Eigenbrot, C.5
Sliwkowski, M.X.6
Klumperman, J.7
Scheller, R.H.8
-
23
-
-
84880733804
-
Bench to bedside translation of antibody drug conjugates using a multiscale mechanistic PK/PD model: A case study with brentuximab-vedotin
-
Shah DK, Haddish-Berhan N, Betts A (2012) Bench to bedside translation of antibody drug conjugates using a multiscale mechanistic PK/PD model: a case study with brentuximab-vedotin. J Pharmacokinet Pharmacodyn 39:643-659
-
(2012)
J Pharmacokinet Pharmacodyn
, vol.39
, pp. 643-659
-
-
Shah, D.K.1
Haddish-Berhan, N.2
Betts, A.3
-
24
-
-
33645500289
-
Anti-body-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker dependent intracellular processing
-
Erickson HK, Park PU, Widdison WC, Kovtun YV, Garrett LM, Hoffman K, Lutz RJ, Goldmacher VS, Blättler WA (2006) Anti-body-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker dependent intracellular processing. Cancer Res 66(8):4426-4433
-
(2006)
Cancer Res
, vol.66
, Issue.8
, pp. 4426-4433
-
-
Erickson, H.K.1
Park, P.U.2
Widdison, W.C.3
Kovtun, Y.V.4
Garrett, L.M.5
Hoffman, K.6
Lutz, R.J.7
Goldmacher, V.S.8
Blättler, W.A.9
-
25
-
-
84866601281
-
Semi-mechanistic population pharmacokinetic model of multivalent trastuzumab emtansine in patients with metastatic breast cancer
-
Chudasama VL, Stark FS, Harrold JM, Tibbetts J, Girish SR, Gupta M, Frey N, Mager DE (2012) Semi-mechanistic population pharmacokinetic model of multivalent trastuzumab emtansine in patients with metastatic breast cancer. Clin Pharmacol Ther 92(4):520-527
-
(2012)
Clin Pharmacol Ther
, vol.92
, Issue.4
, pp. 520-527
-
-
Chudasama, V.L.1
Stark, F.S.2
Harrold, J.M.3
Tibbetts, J.4
Girish, S.R.5
Gupta, M.6
Frey, N.7
Mager, D.E.8
|