-
1
-
-
84906874906
-
Ado-trastuzumab Emtansine (T-DM1): An antibody-drug conjugate (ADC) for HER2-positive breast cancer
-
Lambert, J. M. and Chari, R. V. (2014) Ado-trastuzumab Emtansine (T-DM1): an antibody-drug conjugate (ADC) for HER2-positive breast cancer J. Med. Chem. 57, 6949-64 10.1021/jm500766w
-
(2014)
J. Med. Chem.
, vol.57
, pp. 6949-6964
-
-
Lambert, J.M.1
Chari, R.V.2
-
2
-
-
84863688504
-
The discovery and development of brentuximab vedotin for use in relapsed Hodgkin lymphoma and systemic anaplastic large cell lymphoma
-
Senter, P. D. and Sievers, E. L. (2012) The discovery and development of brentuximab vedotin for use in relapsed Hodgkin lymphoma and systemic anaplastic large cell lymphoma Nat. Biotechnol. 30, 631-7 10.1038/nbt.2289
-
(2012)
Nat. Biotechnol.
, vol.30
, pp. 631-637
-
-
Senter, P.D.1
Sievers, E.L.2
-
3
-
-
6044223544
-
Effects of drug loading on the antitumor activity of a monoclonal antibody drug conjugate
-
Hamblett, K. J., Senter, P. D., Chace, D. F., Sun, M. M., Lenox, J., Cerveny, C. G., Kissler, K. M., Bernhardt, S. X., Kopcha, A. K., and Zabinski, R. F. et al. 2004, Effects of drug loading on the antitumor activity of a monoclonal antibody drug conjugate Clin. Cancer Res. 10, 7063-70 10.1158/1078-0432.CCR-04-0789
-
(2004)
Clin. Cancer Res.
, vol.10
, pp. 7063-7070
-
-
Hamblett, K.J.1
Senter, P.D.2
Chace, D.F.3
Sun, M.M.4
Lenox, J.5
Cerveny, C.G.6
Kissler, K.M.7
Bernhardt, S.X.8
Kopcha, A.K.9
Zabinski, R.F.10
-
4
-
-
84961613545
-
Microscale screening of antibody libraries as maytansinoid antibody-drug conjugates
-
Catcott, K. C., McShea, M. A., Bialucha, C. U., Miller, K. L., Hicks, S. W., Saxena, P., Gesner, T. G., Woldegiorgis, M., Lewis, M. E., and Bai, C. et al. 2016, Microscale screening of antibody libraries as maytansinoid antibody-drug conjugates mAbs 8, 513-23 10.1080/19420862.2015.1134408
-
(2016)
MAbs
, vol.8
, pp. 513-523
-
-
Catcott, K.C.1
McShea, M.A.2
Bialucha, C.U.3
Miller, K.L.4
Hicks, S.W.5
Saxena, P.6
Gesner, T.G.7
Woldegiorgis, M.8
Lewis, M.E.9
Bai, C.10
-
5
-
-
0037068501
-
Monoclonal antibody conjugates of doxorubicin prepared with branched peptide linkers: Inhibition of aggregation by methoxytriethyleneglycol chains
-
King, H. D., Dubowchik, G. M., Mastalerz, H., Willner, D., Hofstead, S. J., Firestone, R. A., Lasch, S. J., and Trail, P. A. (2002) Monoclonal antibody conjugates of doxorubicin prepared with branched peptide linkers: inhibition of aggregation by methoxytriethyleneglycol chains J. Med. Chem. 45, 4336-43 10.1021/jm020149g
-
(2002)
J. Med. Chem.
, vol.45
, pp. 4336-4343
-
-
King, H.D.1
Dubowchik, G.M.2
Mastalerz, H.3
Willner, D.4
Hofstead, S.J.5
Firestone, R.A.6
Lasch, S.J.7
Trail, P.A.8
-
6
-
-
84944441047
-
Reducing hydrophobicity of homogeneous antibody-drug conjugates improves pharmacokinetics and therapeutic index
-
Lyon, R. P., Bovee, T. D., Doronina, S. O., Burke, P. J., Hunter, J. H., Neff-LaFord, H. D., Jonas, M., Anderson, M. E., Setter, J. R., and Senter, P. D. (2015) Reducing hydrophobicity of homogeneous antibody-drug conjugates improves pharmacokinetics and therapeutic index Nat. Biotechnol. 33, 733-5 10.1038/nbt.3212
-
(2015)
Nat. Biotechnol.
, vol.33
, pp. 733-735
-
-
Lyon, R.P.1
Bovee, T.D.2
Doronina, S.O.3
Burke, P.J.4
Hunter, J.H.5
Neff-LaFord, H.D.6
Jonas, M.7
Anderson, M.E.8
Setter, J.R.9
Senter, P.D.10
-
7
-
-
84942888738
-
A Polymer-Based Antibody-Vinca Drug Conjugate Platform: Characterization and Preclinical Efficacy
-
Yurkovetskiy, A. V., Yin, M., Bodyak, N., Stevenson, C. A., Thomas, J. D., Hammond, C. E., Qin, L., Zhu, B., Gumerov, D. R., and Ter-Ovanesyan, E. et al. 2015, A Polymer-Based Antibody-Vinca Drug Conjugate Platform: Characterization and Preclinical Efficacy Cancer Res. 75, 3365-72 10.1158/0008-5472.CAN-15-0129
-
(2015)
Cancer Res.
, vol.75
, pp. 3365-3372
-
-
Yurkovetskiy, A.V.1
Yin, M.2
Bodyak, N.3
Stevenson, C.A.4
Thomas, J.D.5
Hammond, C.E.6
Qin, L.7
Zhu, B.8
Gumerov, D.R.9
Ter-Ovanesyan, E.10
-
8
-
-
84942085714
-
IMGN853, a folate receptor alpha (FRalpha)-targeting antibody-drug conjugate, exhibits potent targeted anti-tumor activity against FRalpha-expressing tumors
-
Ab, O., Whiteman, K. R., Bartle, L. M., Sun, X., Singh, R., Tavares, D., LaBelle, A., Payne, G., Lutz, R. J., and Pinkas, J., et al., (2015) IMGN853, a folate receptor alpha (FRalpha)-targeting antibody-drug conjugate, exhibits potent targeted anti-tumor activity against FRalpha-expressing tumors. Mol. Cancer Ther.. 14, 1605 10.1158/1535-7163.MCT-14-1095
-
(2015)
Mol. Cancer Ther.
, vol.14
, pp. 1605
-
-
Ab, O.1
Whiteman, K.R.2
Bartle, L.M.3
Sun, X.4
Singh, R.5
Tavares, D.6
LaBelle, A.7
Payne, G.8
Lutz, R.J.9
Pinkas, J.10
-
9
-
-
64949125849
-
Antibody-cytotoxic agent conjugates: Preparation and characterization
-
xiv
-
Singh, R. and Erickson, H. K. (2009) Antibody-cytotoxic agent conjugates: preparation and characterization Methods Mol. Biol. 525, 445-67 xiv. 10.1007/978-1-59745-554-1-23
-
(2009)
Methods Mol. Biol.
, vol.525
, pp. 445-467
-
-
Singh, R.1
Erickson, H.K.2
-
10
-
-
84930685746
-
Statistics of the Distribution of the Abundance of Molecules with Various Drug Loads in Maytansinoid Antibody-Drug Conjugates
-
Goldmacher, V. S., Amphlett, G., Wang, L., and Lazar, A. C. (2015) Statistics of the Distribution of the Abundance of Molecules with Various Drug Loads in Maytansinoid Antibody-Drug Conjugates. Mol. Pharmaceutics. 12, 1738 10.1021/mp5007536
-
(2015)
Mol. Pharmaceutics
, vol.12
, pp. 1738
-
-
Goldmacher, V.S.1
Amphlett, G.2
Wang, L.3
Lazar, A.C.4
-
11
-
-
34547935736
-
Cell killing by antibody-drug conjugates
-
Kovtun, Y. V. and Goldmacher, V. S. (2007) Cell killing by antibody-drug conjugates Cancer Lett. 255, 232-40 10.1016/j.canlet.2007.04.010
-
(2007)
Cancer Lett.
, vol.255
, pp. 232-240
-
-
Kovtun, Y.V.1
Goldmacher, V.S.2
-
12
-
-
33645500289
-
Antibody-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker-dependent intracellular processing
-
Erickson, H. K., Park, P. U., Widdison, W. C., Kovtun, Y. V., Garrett, L. M., Hoffman, K., Lutz, R. J., Goldmacher, V. S., and Blattler, W. A. (2006) Antibody-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker-dependent intracellular processing Cancer Res. 66, 4426-33
-
(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
Blattler, W.A.9
-
13
-
-
74949139946
-
Tumor delivery and in vivo processing of disulfide-linked and thioether-linked antibody-maytansinoid conjugates
-
Erickson, H. K., Widdison, W. C., Mayo, M. F., Whiteman, K., Audette, C., Wilhelm, S. D., and Singh, R. (2010) Tumor delivery and in vivo processing of disulfide-linked and thioether-linked antibody-maytansinoid conjugates Bioconjugate Chem. 21, 84-92 10.1021/bc900315y
-
(2010)
Bioconjugate 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
-
14
-
-
1342287215
-
Pharmacokinetics and biodistribution of the antitumor immunoconjugate, cantuzumab mertansine (huC242-DM1), and its two components in mice
-
Xie, H., Audette, C., Hoffee, M., Lambert, J. M., and Blattler, W. A. (2003) Pharmacokinetics and biodistribution of the antitumor immunoconjugate, cantuzumab mertansine (huC242-DM1), and its two components in mice J. Pharmacol. Exp. Ther. 308, 1073-1082 10.1124/jpet.103.060533
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.308
, pp. 1073-1082
-
-
Xie, H.1
Audette, C.2
Hoffee, M.3
Lambert, J.M.4
Blattler, W.A.5
-
15
-
-
76049122850
-
Intracellular activation of SGN-35, a potent anti-CD30 antibody-drug conjugate
-
Okeley, N. M., Miyamoto, J. B., Zhang, X., Sanderson, R. J., Benjamin, D. R., Sievers, E. L., Senter, P. D., and Alley, S. C. (2010) Intracellular activation of SGN-35, a potent anti-CD30 antibody-drug conjugate Clin. Cancer Res. 16, 888-97 10.1158/1078-0432.CCR-09-2069
-
(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
-
16
-
-
84942502479
-
Site-specific conjugation improves therapeutic index of antibody drug conjugates with high drug loading
-
Strop, P., Delaria, K., Foletti, D., Witt, J. M., Hasa-Moreno, A., Poulsen, K., Casas, M. G., Dorywalska, M., Farias, S., and Pios, A. et al. 2015, Site-specific conjugation improves therapeutic index of antibody drug conjugates with high drug loading Nat. Biotechnol. 33, 694-6 10.1038/nbt.3274
-
(2015)
Nat. Biotechnol.
, vol.33
, pp. 694-696
-
-
Strop, P.1
Delaria, K.2
Foletti, D.3
Witt, J.M.4
Hasa-Moreno, A.5
Poulsen, K.6
Casas, M.G.7
Dorywalska, M.8
Farias, S.9
Pios, A.10
-
17
-
-
24344456964
-
Structural characterization of the maytansinoid-monoclonal antibody immunoconjugate, huN901-DM1, by mass spectrometry
-
Wang, L., Amphlett, G., Blattler, W. A., Lambert, J. M., and Zhang, W. (2005) Structural characterization of the maytansinoid-monoclonal antibody immunoconjugate, huN901-DM1, by mass spectrometry Protein Sci. 14, 2436-46 10.1110/ps.051478705
-
(2005)
Protein Sci.
, vol.14
, pp. 2436-2446
-
-
Wang, L.1
Amphlett, G.2
Blattler, W.A.3
Lambert, J.M.4
Zhang, W.5
-
18
-
-
84904417255
-
Statistical modeling of the drug load distribution on trastuzumab emtansine (Kadcyla), a lysine-linked antibody drug conjugate
-
Kim, M. T., Chen, Y., Marhoul, J., and Jacobson, F. (2014) Statistical modeling of the drug load distribution on trastuzumab emtansine (Kadcyla), a lysine-linked antibody drug conjugate Bioconjugate Chem. 25, 1223-32 10.1021/bc5000109
-
(2014)
Bioconjugate Chem.
, vol.25
, pp. 1223-1232
-
-
Kim, M.T.1
Chen, Y.2
Marhoul, J.3
Jacobson, F.4
-
19
-
-
84959456912
-
New developments for antibody-drug conjugate-based therapeutic approaches
-
de Goeij, B. E. and Lambert, J. M. (2016) New developments for antibody-drug conjugate-based therapeutic approaches Curr. Opin. Immunol. 40, 14-23 10.1016/j.coi.2016.02.008
-
(2016)
Curr. Opin. Immunol.
, vol.40
, pp. 14-23
-
-
De Goeij, B.E.1
Lambert, J.M.2
-
20
-
-
84925436590
-
A mechanistic tumor penetration model to guide antibody drug conjugate design
-
Vasalou, C., Helmlinger, G., and Gomes, B. (2015) A mechanistic tumor penetration model to guide antibody drug conjugate design PLoS One 10, e0118977 10.1371/journal.pone.0118977
-
(2015)
PLoS One
, vol.10
, pp. e0118977
-
-
Vasalou, C.1
Helmlinger, G.2
Gomes, B.3
-
21
-
-
84973622912
-
Multiscale Modeling of Antibody-Drug Conjugates: Connecting Tissue and Cellular Distribution to Whole Animal Pharmacokinetics and Potential Implications for Efficacy
-
Cilliers, C., Guo, H., Liao, J., Christodolu, N., and Thurber, G. M. (2016) Multiscale Modeling of Antibody-Drug Conjugates: Connecting Tissue and Cellular Distribution to Whole Animal Pharmacokinetics and Potential Implications for Efficacy AAPS J. 18, 1117-30 10.1208/s12248-016-9940-z
-
(2016)
AAPS J.
, vol.18
, pp. 1117-1130
-
-
Cilliers, C.1
Guo, H.2
Liao, J.3
Christodolu, N.4
Thurber, G.M.5
-
22
-
-
79957730092
-
Synthesis and evaluation of hydrophilic linkers for antibody-maytansinoid conjugates
-
Zhao, R. Y., Wilhelm, S. D., Audette, C., Jones, G., Leece, B. A., Lazar, A. C., Goldmacher, V. S., Singh, R., Kovtun, Y., and Widdison, W. C. et al. 2011, Synthesis and evaluation of hydrophilic linkers for antibody-maytansinoid conjugates J. Med. Chem. 54, 3606-23 10.1021/jm2002958
-
(2011)
J. Med. Chem.
, vol.54
, pp. 3606-3623
-
-
Zhao, R.Y.1
Wilhelm, S.D.2
Audette, C.3
Jones, G.4
Leece, B.A.5
Lazar, A.C.6
Goldmacher, V.S.7
Singh, R.8
Kovtun, Y.9
Widdison, W.C.10
-
23
-
-
21244469077
-
Analysis of the composition of immunoconjugates using size-exclusion chromatography coupled to mass spectrometry
-
Lazar, A. C., Wang, L., Blattler, W. A., Amphlett, G., Lambert, J. M., and Zhang, W. (2005) Analysis of the composition of immunoconjugates using size-exclusion chromatography coupled to mass spectrometry Rapid Commun. Mass Spectrom. 19, 1806-14 10.1002/rcm.1987
-
(2005)
Rapid Commun. Mass Spectrom.
, vol.19
, pp. 1806-1814
-
-
Lazar, A.C.1
Wang, L.2
Blattler, W.A.3
Amphlett, G.4
Lambert, J.M.5
Zhang, W.6
-
24
-
-
84979521089
-
Understanding How the Stability of the Thiol-Maleimide Linkage Impacts the Pharmacokinetics of Lysine-Linked Antibody-Maytansinoid Conjugates
-
Ponte, J. F., Sun, X., Yoder, N. C., Fishkin, N., Laleau, R., Coccia, J., Lanieri, L., Bogalhas, M., Wang, L., and Wilhelm, S. et al. 2016, Understanding How the Stability of the Thiol-Maleimide Linkage Impacts the Pharmacokinetics of Lysine-Linked Antibody-Maytansinoid Conjugates Bioconjugate Chem. 27, 1588-98 10.1021/acs.bioconjchem.6b00117
-
(2016)
Bioconjugate Chem.
, vol.27
, pp. 1588-1598
-
-
Ponte, J.F.1
Sun, X.2
Yoder, N.C.3
Fishkin, N.4
Laleau, R.5
Coccia, J.6
Lanieri, L.7
Bogalhas, M.8
Wang, L.9
Wilhelm, S.10
-
25
-
-
0024354304
-
Determination of subcutaneous tumor size in athymic (nude) mice
-
Tomayko, M. M. and Reynolds, C. P. (1989) Determination of subcutaneous tumor size in athymic (nude) mice Cancer Chemother. Pharmacol. 24, 148-54 10.1007/BF00300234
-
(1989)
Cancer Chemother. Pharmacol.
, vol.24
, pp. 148-154
-
-
Tomayko, M.M.1
Reynolds, C.P.2
-
26
-
-
0026425674
-
Experimental antitumor activity of taxotere (RP 56976, NSC 628503), a taxol analogue
-
Bissery, M. C., Guenard, D., Gueritte-Voegelein, F., and Lavelle, F. (1991) Experimental antitumor activity of taxotere (RP 56976, NSC 628503), a taxol analogue Cancer Res. 51, 4845-52
-
(1991)
Cancer Res.
, vol.51
, pp. 4845-4852
-
-
Bissery, M.C.1
Guenard, D.2
Gueritte-Voegelein, F.3
Lavelle, F.4
|