-
1
-
-
49449119098
-
Antibody-drug conjugates for cancer therapy
-
Carter, P. J., and Senter, P. D. (2008) Antibody-drug conjugates for cancer therapy. Cancer J. 14, 154-69.
-
(2008)
Cancer J
, vol.14
, pp. 154-169
-
-
Carter, P.J.1
Senter, P.D.2
-
2
-
-
38949192547
-
Targeted cancer therapy: Conferring specificity to cytotoxic drugs
-
Chari, R. V. (2008) Targeted cancer therapy: conferring specificity to cytotoxic drugs. Acc. Chem. Res. 41, 98-107.
-
(2008)
Acc. Chem. Res
, vol.41
, pp. 98-107
-
-
Chari, R.V.1
-
3
-
-
40949103761
-
A phase I study of trastuzumab-MCC-DM1 (T-DM1), a first-in-class HER2 antibody-drug conjugate (ADC), in patients (pts) with HER2+ metastatic breast cancer (BC)
-
Abstract 1042
-
Beeram, M., Krop, I., Modi, S., Tolcher, A., Rabbee, N., Girish, S., Tibbitts, J., Holden, S., Lutzker, S., and Burris, H. (2007) A phase I study of trastuzumab-MCC-DM1 (T-DM1), a first-in-class HER2 antibody-drug conjugate (ADC), in patients (pts) with HER2+ metastatic breast cancer (BC). J. Clin. Oncol. 25, Abstract 1042.
-
(2007)
J. Clin. Oncol
, vol.25
-
-
Beeram, M.1
Krop, I.2
Modi, S.3
Tolcher, A.4
Rabbee, N.5
Girish, S.6
Tibbitts, J.7
Holden, S.8
Lutzker, S.9
Burris, H.10
-
4
-
-
84930170960
-
A phase I study of trastuzumab-DM1, a first-in-class HER2 antibody-drug conjugate, in patients with advanced HER2+ breast cancer
-
Abstract 310
-
Krop, I. E., Beeram, M., Modi, S., Rabbee, N., Girish, S., Tibbitts, J., Holden, S. N., Lutzker, S. G., and Burris, H. A. (2007) A phase I study of trastuzumab-DM1, a first-in-class HER2 antibody-drug conjugate, in patients with advanced HER2+ breast cancer, In 30th Annual San Antonio Breast Cancer Symposium, Abstract 310.
-
(2007)
30th Annual San Antonio Breast Cancer Symposium
-
-
Krop, I.E.1
Beeram, M.2
Modi, S.3
Rabbee, N.4
Girish, S.5
Tibbitts, J.6
Holden, S.N.7
Lutzker, S.G.8
Burris, H.A.9
-
5
-
-
55249084785
-
A novel antibody-drug conjugate, SGN-35, (anti-CD30-auristatin), induces objective responses in patients with relapsed or refractory Hodgkin lymphoma, preliminary results of a phase I tolerability study
-
Younes, A., Forero-Torres, A., Bartlett, N., Leonard, J. P., Rege, B., Kennedy, D. A., Lorenz, J., and Sievers, E. L. (2007) A novel antibody-drug conjugate, SGN-35, (anti-CD30-auristatin), induces objective responses in patients with relapsed or refractory Hodgkin lymphoma, preliminary results of a phase I tolerability study, In 7th International Symposium on Hodgkin Lymphoma.
-
(2007)
7th International Symposium on Hodgkin Lymphoma
-
-
Younes, A.1
Forero-Torres, A.2
Bartlett, N.3
Leonard, J.P.4
Rege, B.5
Kennedy, D.A.6
Lorenz, J.7
Sievers, E.L.8
-
6
-
-
53349093644
-
Objective responses in a phase I dose-escalation study of SGN-35, a novel antibody-drug conjugate (ADC) targeting CD30, in patients with relapsed or refractory hodgkin lymphoma
-
Younes, A., Forero-Torres, A., Bartlett, N. L., Leonard, J. P., Rege, B., Kennedy, D. A., Lorenz, J. M., and Sievers, E. L. (2008) Objective responses in a phase I dose-escalation study of SGN-35, a novel antibody-drug conjugate (ADC) targeting CD30, in patients with relapsed or refractory hodgkin lymphoma. Am. Soc. Clin. Oncol.
-
(2008)
Am. Soc. Clin. Oncol
-
-
Younes, A.1
Forero-Torres, A.2
Bartlett, N.L.3
Leonard, J.P.4
Rege, B.5
Kennedy, D.A.6
Lorenz, J.M.7
Sievers, E.L.8
-
7
-
-
10744222473
-
Development of potent monoclonal antibody auristatin conjugates for cancer therapy
-
Doronina, S. O., Toki, B. E., Torgov, M. Y., Mendelsohn, B. A., Cerveny, C. G., Chace, D. F., DeBlanc, R. L., Gearing, R. P., Bovee, T. D., Siegall, C. B., Francisco, J. A., Wahl, A. F., Meyer, D. L., and Senter, P. D. (2003) Development of potent monoclonal antibody auristatin conjugates for cancer therapy. Nat. Biotechnol. 21, 778-84.
-
(2003)
Nat. Biotechnol
, vol.21
, pp. 778-784
-
-
Doronina, S.O.1
Toki, B.E.2
Torgov, M.Y.3
Mendelsohn, B.A.4
Cerveny, C.G.5
Chace, D.F.6
DeBlanc, R.L.7
Gearing, R.P.8
Bovee, T.D.9
Siegall, C.B.10
Francisco, J.A.11
Wahl, A.F.12
Meyer, D.L.13
Senter, P.D.14
-
8
-
-
12244295755
-
In vivo drug-linker stability of an anti-CD30 dipeptide-linked auristatin immunoconjugate
-
Sanderson, R. J., Hering, M. A., James, S. F., Sun, M. M., Doronina, S. O., Siadak, A. W., Senter, P. D., and Wahl, A. F. (2005) In vivo drug-linker stability of an anti-CD30 dipeptide-linked auristatin immunoconjugate. Clin. Cancer Res. 11, 843-52.
-
(2005)
Clin. Cancer Res
, vol.11
, pp. 843-852
-
-
Sanderson, R.J.1
Hering, M.A.2
James, S.F.3
Sun, M.M.4
Doronina, S.O.5
Siadak, A.W.6
Senter, P.D.7
Wahl, A.F.8
-
9
-
-
0042738861
-
cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity
-
Francisco, J. A., Cerveny, C. G., Meyer, D. L., Mixan, B. J., Klussman, K., Chace, D. F., Rejniak, S. X., Gordon, K. A., DeBlanc, R., Toki, B. E., Law, C. L., Doronina, S. O., Siegall, C. B., Senter, P. D., and Wahl, A. F. (2003) cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity. Blood 102, 1458-65.
-
(2003)
Blood
, vol.102
, pp. 1458-1465
-
-
Francisco, J.A.1
Cerveny, C.G.2
Meyer, D.L.3
Mixan, B.J.4
Klussman, K.5
Chace, D.F.6
Rejniak, S.X.7
Gordon, K.A.8
DeBlanc, R.9
Toki, B.E.10
Law, C.L.11
Doronina, S.O.12
Siegall, C.B.13
Senter, P.D.14
Wahl, A.F.15
-
10
-
-
31544441685
-
Enhanced activity of monomethylauristatin F through monoclonal antibody delivery: Effects of linker technology on efficacy and toxicity
-
Doronina, S. O., Mendelsohn, B. A., Bovee, T. D., Cerveny, C. G., Alley, S. C., Meyer, D. L., Oflazoglu, E., Toki, B. E., Sanderson, R. J., Zabinski, R. F., Wahl, A. F., and Senter, P. D. (2006) Enhanced activity of monomethylauristatin F through monoclonal antibody delivery: effects of linker technology on efficacy and toxicity. Bioconjugate Chem. 17, 114-24.
-
(2006)
Bioconjugate 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
-
11
-
-
27944502827
-
Dipeptide-based highly potent doxorubicin antibody conjugates
-
Jeffrey, S. C., Nguyen, M. T., Andreyka, J. B., Meyer, D. L., Doronina, S. O., and Senter, P. D. (2006) Dipeptide-based highly potent doxorubicin antibody conjugates. Bioorg. Med. Chem. Lett. 16, 358-62.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 358-362
-
-
Jeffrey, S.C.1
Nguyen, M.T.2
Andreyka, J.B.3
Meyer, D.L.4
Doronina, S.O.5
Senter, P.D.6
-
12
-
-
33947577845
-
Minor groove binder antibody conjugates employing a water soluble beta-glucuronide linker
-
Jeffrey, S. C., Nguyen, M. T., Moser, R. F., Meyer, D. L., Miyamoto, J. B., and Senter, P. D. (2007) Minor groove binder antibody conjugates employing a water soluble beta-glucuronide linker. Bioorg. Med. Chem. Lett. 17, 2278-80.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 2278-2280
-
-
Jeffrey, S.C.1
Nguyen, M.T.2
Moser, R.F.3
Meyer, D.L.4
Miyamoto, J.B.5
Senter, P.D.6
-
13
-
-
33644505446
-
Lymphocyte activation antigen CD70 expressed by renal cell carcinoma is a potential therapeutic target for anti-CD70 antibody-drug conjugates
-
Law, C. L., Gordon, K. A., Toki, B. E., Yamane, A. K., Hering, M. A., Cerveny, C. G., Petroziello, J. M., Ryan, M. C., Smith, L., Simon, R., Sauter, G., Oflazoglu, E., Doronina, S. O., Meyer, D. L., Francisco, J. A., Carter, P., Senter, P. D., Copland, J. A., Wood, C. G., and Wahl, A. F. (2006) Lymphocyte activation antigen CD70 expressed by renal cell carcinoma is a potential therapeutic target for anti-CD70 antibody-drug conjugates. Cancer Res. 66, 2328-37.
-
(2006)
Cancer Res
, vol.66
, pp. 2328-2337
-
-
Law, C.L.1
Gordon, K.A.2
Toki, B.E.3
Yamane, A.K.4
Hering, M.A.5
Cerveny, C.G.6
Petroziello, J.M.7
Ryan, M.C.8
Smith, L.9
Simon, R.10
Sauter, G.11
Oflazoglu, E.12
Doronina, S.O.13
Meyer, D.L.14
Francisco, J.A.15
Carter, P.16
Senter, P.D.17
Copland, J.A.18
Wood, C.G.19
Wahl, A.F.20
more..
-
14
-
-
25444507922
-
Reduction-alkylation strategies for the modification of specific monoclonal antibody disulfides
-
Sun, M. M., Beam, K. S., Cerveny, C. G., Hamblett, K. J., Blackmore, R. S., Torgov, M. Y., Handley, F. G., Ihle, N. C., Senter, P. D., and Alley, S. C. (2005) Reduction-alkylation strategies for the modification of specific monoclonal antibody disulfides. Bioconjugate Chem. 16, 1282-90.
-
(2005)
Bioconjugate Chem
, vol.16
, pp. 1282-1290
-
-
Sun, M.M.1
Beam, K.S.2
Cerveny, C.G.3
Hamblett, K.J.4
Blackmore, R.S.5
Torgov, M.Y.6
Handley, F.G.7
Ihle, N.C.8
Senter, P.D.9
Alley, S.C.10
-
15
-
-
41149160183
-
Contribution of linker stability to the activities of anticancer immunoconjugates
-
Alley, S. C., Benjamin, D. R., Jeffrey, S. C., Okeley, N. M., Meyer, D. L., Sanderson, R. J., and Senter, P. D. (2008) Contribution of linker stability to the activities of anticancer immunoconjugates. Bioconjugate Chem. 19, 759-65.
-
(2008)
Bioconjugate Chem
, vol.19
, pp. 759-765
-
-
Alley, S.C.1
Benjamin, D.R.2
Jeffrey, S.C.3
Okeley, N.M.4
Meyer, D.L.5
Sanderson, R.J.6
Senter, P.D.7
-
16
-
-
35148827486
-
Auristatin PYE, a novel synthetic derivative of dolastatin 10, is highly effective in human colon tumour models
-
Shnyder, S. D., Cooper, P. A., Millington, N. J., Pettit, G. R., and Bibby, M. C. (2007) Auristatin PYE, a novel synthetic derivative of dolastatin 10, is highly effective in human colon tumour models. Int. J. Oncol. 31, 353-60.
-
(2007)
Int. J. Oncol
, vol.31
, pp. 353-360
-
-
Shnyder, S.D.1
Cooper, P.A.2
Millington, N.J.3
Pettit, G.R.4
Bibby, M.C.5
-
17
-
-
0032402354
-
Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin
-
Dubowchik, G. M., and Firestone, R. A. (1998) Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin. Bioorg. Med. Chem. Lett. 8, 3341-6.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 3341-3346
-
-
Dubowchik, G.M.1
Firestone, R.A.2
-
18
-
-
0032402572
-
Cathepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs paclitaxel (Taxol), mitomycin C and doxorubicin
-
Dubowchik, G. M., Mosure, K., Knipe, J. O., and Firestone, R. A. (1998) Cathepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs paclitaxel (Taxol), mitomycin C and doxorubicin. Bioorg. Med. Chem. Lett. 8, 3347-52.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 3347-3352
-
-
Dubowchik, G.M.1
Mosure, K.2
Knipe, J.O.3
Firestone, R.A.4
-
19
-
-
0033180164
-
Receptor-mediated and enzyme-dependent targeting of cytotoxic anticancer drugs
-
Dubowchik, G. M., and Walker, M. A. (1999) Receptor-mediated and enzyme-dependent targeting of cytotoxic anticancer drugs. Pharmacol. Ther. 83, 67-123.
-
(1999)
Pharmacol. Ther
, vol.83
, pp. 67-123
-
-
Dubowchik, G.M.1
Walker, M.A.2
|