-
1
-
-
0015462030
-
Combination cancer therapy: Presidential address
-
Frei E III. Combination cancer therapy: presidential address. Cancer Res 1972;32:2593-607.
-
(1972)
Cancer Res
, vol.32
, pp. 2593-2607
-
-
Frei E, I.I.I.1
-
3
-
-
0033002547
-
Phase I trial of dolastatin-10 (NSC 376128) in patients with advanced solid tumors
-
Pitot HC, McElroy EA Jr, Reid JM, Windebank AJ, Sloan JA, Erlichman C, et al. Phase I trial of dolastatin-10 (NSC 376128) in patients with advanced solid tumors. Clin Cancer Res 1999;5:525-31.
-
(1999)
Clin Cancer Res
, vol.5
, pp. 525-531
-
-
Pitot, H.C.1
McElroy, E.A.2
Reid, J.M.3
Windebank, A.J.4
Sloan, J.A.5
Erlichman, C.6
-
4
-
-
0037316411
-
Phase 2 study of cryptophycin 52 (LY355703) in patients previously treated with platinum based chemotherapy for advanced non-small cell lung cancer
-
Edelman MJ, Gandara DR, Hausner P, Israel V, Thornton D, DeSanto J, et al. Phase 2 study of cryptophycin 52 (LY355703) in patients previously treated with platinum based chemotherapy for advanced non-small cell lung cancer. Lung Cancer 2003;39:197-9.
-
(2003)
Lung Cancer
, vol.39
, pp. 197-199
-
-
Edelman, M.J.1
Gandara, D.R.2
Hausner, P.3
Israel, V.4
Thornton, D.5
DeSanto, J.6
-
5
-
-
0031731907
-
Phase II study of adozelesin in untreated metastatic breast cancer
-
Cristofanilli M, Bryan WJ, Miller LL, Chang AY, Gradishar WJ, Kufe DW, et al. Phase II study of adozelesin in untreated metastatic breast cancer. Anticancer Drugs 1998;9:779-82.
-
(1998)
Anticancer Drugs
, vol.9
, pp. 779-782
-
-
Cristofanilli, M.1
Bryan, W.J.2
Miller, L.L.3
Chang, A.Y.4
Gradishar, W.J.5
Kufe, D.W.6
-
6
-
-
0036304763
-
A Phase I study of bizelesin (NSC 615291) in patients with advanced solid tumors
-
Pitot HC, Reid JM, Sloan JA, Ames MM, Adjei AA, Rubin J, et al. A Phase I study of bizelesin (NSC 615291) in patients with advanced solid tumors. Clin Cancer Res 2002;8:712-7.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 712-717
-
-
Pitot, H.C.1
Reid, J.M.2
Sloan, J.A.3
Ames, M.M.4
Adjei, A.A.5
Rubin, J.6
-
7
-
-
84898066972
-
Antibody-drug conjugates: An emerging concept in cancer therapy
-
Chari RV, Miller ML, Widdison WC. Antibody-drug conjugates: An emerging concept in cancer therapy. Angewandte Chemie 2014;53: 3796-827.
-
(2014)
Angewandte Chemie
, vol.53
, pp. 3796-3827
-
-
Chari, R.V.1
Miller, M.L.2
Widdison, W.C.3
-
8
-
-
84955494300
-
Recent advances in the construction of antibody-drug conjugates
-
Chudasama V, Maruani A, Caddick S. Recent advances in the construction of antibody-drug conjugates. Nat Chem 2016;8:114-9.
-
(2016)
Nat Chem
, vol.8
, pp. 114-119
-
-
Chudasama, V.1
Maruani, A.2
Caddick, S.3
-
9
-
-
84953431794
-
Antibody-drug conjugates-an emerging class of cancer treatment
-
Diamantis N, Banerji U. Antibody-drug conjugates-an emerging class of cancer treatment. Br J Cancer 2016;114:362-7.
-
(2016)
Br J Cancer
, vol.114
, pp. 362-367
-
-
Diamantis, N.1
Banerji, U.2
-
10
-
-
38949192547
-
Targeted cancer therapy: Conferring specificity to cytotoxic drugs
-
Chari RVJ. Targeted cancer therapy: conferring specificity to cytotoxic drugs. Acc Chem Res 2008;41:98-107.
-
(2008)
Acc Chem Res
, vol.41
, pp. 98-107
-
-
Chari, R.V.J.1
-
11
-
-
84873053339
-
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
-
13
-
-
84936074960
-
FDA approval: Ado-trastuzumab emtansine for the treatment of patients with HER2-positive metastatic breast cancer
-
Amiri-Kordestani L, Blumenthal GM, Xu QC, Zhang L, Tang SW, Ha L, et al. FDA approval: ado-trastuzumab emtansine for the treatment of patients with HER2-positive metastatic breast cancer. Clin Cancer Res 2014;20: 4436-41.
-
(2014)
Clin Cancer Res
, vol.20
, pp. 4436-4441
-
-
Amiri-Kordestani, L.1
Blumenthal, G.M.2
Xu, Q.C.3
Zhang, L.4
Tang, S.W.5
Ha, L.6
-
14
-
-
84906874906
-
Ado-trastuzumab Emtansine (T-DM1): An antibody-drug conjugate (ADC) for HER2-positive breast cancer
-
Lambert JM, Chari RV. Ado-trastuzumab Emtansine (T-DM1): an antibody-drug conjugate (ADC) for HER2-positive breast cancer. J Med Chem 2014;57:6949-64.
-
(2014)
J Med Chem
, vol.57
, pp. 6949-6964
-
-
Lambert, J.M.1
Chari, R.V.2
-
15
-
-
84881305790
-
A phase 3 study of gemtuzumab ozogamicin during induction and postconsolidation therapy in younger patients with acute myeloid leukemia
-
Petersdorf SH, Kopecky KJ, Slovak M, Willman C, Nevill T, Brandwein J, et al. A phase 3 study of gemtuzumab ozogamicin during induction and postconsolidation therapy in younger patients with acute myeloid leukemia. Blood 2013;121:4854-60.
-
(2013)
Blood
, vol.121
, pp. 4854-4860
-
-
Petersdorf, S.H.1
Kopecky, K.J.2
Slovak, M.3
Willman, C.4
Nevill, T.5
Brandwein, J.6
-
16
-
-
84940403711
-
A DLL3-targeted antibody-drug conjugate eradicates high-grade pulmonary neuroendocrine tumor-initiating cells in vivo
-
Saunders LR, Bankovich AJ, Anderson WC, Aujay MA, Bheddah S, Black K, et al. A DLL3-targeted antibody-drug conjugate eradicates high-grade pulmonary neuroendocrine tumor-initiating cells in vivo. Sci Transl Med 2015;7:302ra136.
-
(2015)
Sci Transl Med
, vol.7
, pp. 302ra136
-
-
Saunders, L.R.1
Bankovich, A.J.2
Anderson, W.C.3
Aujay, M.A.4
Bheddah, S.5
Black, K.6
-
17
-
-
84886825064
-
SGN-CD33A: A novel CD33-targeting antibody-drug conjugate utilizing a pyrrolobenzodiazepine dimer is active in models of drug-resistant AML
-
Kung Sutherland MS, Walter RB, Jeffrey SC, Burke PJ, Yu C, Kostner H, et al. SGN-CD33A: a novel CD33-targeting antibody-drug conjugate utilizing a pyrrolobenzodiazepine dimer is active in models of drug-resistant AML. Blood 2013;122:1455-63.
-
(2013)
Blood
, vol.122
, pp. 1455-1463
-
-
Kung Sutherland, M.S.1
Walter, R.B.2
Jeffrey, S.C.3
Burke, P.J.4
Yu, C.5
Kostner, H.6
-
18
-
-
84880380678
-
A potent anti-CD70 antibody-drug conjugate combining a dimeric pyrrolobenzodiazepine drug with site-specific conjugation technology
-
Jeffrey SC, Burke PJ, Lyon RP, Meyer DW, Sussman D, Anderson M, et al. A potent anti-CD70 antibody-drug conjugate combining a dimeric pyrrolobenzodiazepine drug with site-specific conjugation technology. Bioconjug Chem 2013;24:1256-63.
-
(2013)
Bioconjug Chem
, vol.24
, pp. 1256-1263
-
-
Jeffrey, S.C.1
Burke, P.J.2
Lyon, R.P.3
Meyer, D.W.4
Sussman, D.5
Anderson, M.6
-
19
-
-
63449133609
-
Phase I study of sequence-selective minor groove DNA binding agent SJG-136 in patients with advanced solid tumors
-
Hochhauser D, Meyer T, Spanswick VJ, Wu J, Clingen PH, Loadman P, et al. Phase I study of sequence-selective minor groove DNA binding agent SJG-136 in patients with advanced solid tumors. Clin Cancer Res 2009;15: 2140-7.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 2140-2147
-
-
Hochhauser, D.1
Meyer, T.2
Spanswick, V.J.3
Wu, J.4
Clingen, P.H.5
Loadman, P.6
-
20
-
-
33745847797
-
Semisynthetic maytansine analogues for the targeted treatment of cancer
-
Widdison WC, Wilhelm SD, Cavanagh EE, Whiteman KR, Leece BA, Kovtun Y, et al. Semisynthetic maytansine analogues for the targeted treatment of cancer. J Med Chem 2006;49:4392-408.
-
(2006)
J Med Chem
, vol.49
, pp. 4392-4408
-
-
Widdison, W.C.1
Wilhelm, S.D.2
Cavanagh, E.E.3
Whiteman, K.R.4
Leece, B.A.5
Kovtun, Y.6
-
21
-
-
79957730092
-
Synthesis and evaluation of hydrophilic linkers for antibody-maytansinoid conjugates
-
Zhao RY, Wilhelm SD, Audette C, Jones G, Leece BA, Lazar AC, et al. Synthesis and evaluation of hydrophilic linkers for antibody-maytansinoid conjugates. J Med Chem 2011;54:3606-23.
-
(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
-
22
-
-
77950224905
-
Antibody-maytansinoid conjugates designed to bypass multidrug resistance
-
Kovtun YV, Audette CA, Mayo MF, Jones GE, Doherty H, Maloney EK, et al. Antibody-maytansinoid conjugates designed to bypass multidrug resistance. Cancer Res 2010;70:2528-37.
-
(2010)
Cancer Res
, vol.70
, pp. 2528-2537
-
-
Kovtun, Y.V.1
Audette, C.A.2
Mayo, M.F.3
Jones, G.E.4
Doherty, H.5
Maloney, E.K.6
-
23
-
-
4644353500
-
SJG-136 (NSC 694501), a novel rationally designed DNA minor groove interstrand cross-linking agent with potent and broad spectrum antitumor activity: Part 1: Cellular pharmacology, in vitro and initial in vivo antitumor activity
-
Hartley JA, Spanswick VJ, Brooks N, Clingen PH, McHugh PJ, Hochhauser D, et al. SJG-136 (NSC 694501), a novel rationally designed DNA minor groove interstrand cross-linking agent with potent and broad spectrum antitumor activity: part 1: cellular pharmacology, in vitro and initial in vivo antitumor activity. Cancer Res 2004;64:6693-9.
-
(2004)
Cancer Res
, vol.64
, pp. 6693-6699
-
-
Hartley, J.A.1
Spanswick, V.J.2
Brooks, N.3
Clingen, P.H.4
McHugh, P.J.5
Hochhauser, D.6
-
24
-
-
84867619210
-
The vascular disrupting agent STA-9584 exhibits potent antitumor activity by selectively targeting microvasculature at both the center and periphery of tumors
-
Foley KP, Zhou D, Borella C, Wu Y, Zhang M, Jiang J, et al. The vascular disrupting agent STA-9584 exhibits potent antitumor activity by selectively targeting microvasculature at both the center and periphery of tumors. J Pharmacol Exp Ther 2012;343:529-38.
-
(2012)
J Pharmacol Exp Ther
, vol.343
, pp. 529-538
-
-
Foley, K.P.1
Zhou, D.2
Borella, C.3
Wu, Y.4
Zhang, M.5
Jiang, J.6
-
25
-
-
0026425674
-
Experimental antitumor activity of taxotere (RP 56976, NSC 628503), a taxol analogue
-
Bissery MC, Guenard D, Gueritte-Voegelein F, Lavelle F. Experimental antitumor activity of taxotere (RP 56976, NSC 628503), a taxol analogue. Cancer Res 1991;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
-
26
-
-
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, et al. Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate. Cancer Res 2008;68:9280-90.
-
(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
-
27
-
-
33644787435
-
Antibody-drug conjugates designed to eradicate tumors with homogeneous and heterogeneous expression of the target antigen
-
Kovtun YV, Audette CA, Ye Y, Xie H, Ruberti MF, Phinney SJ, et al. Antibody-drug conjugates designed to eradicate tumors with homogeneous and heterogeneous expression of the target antigen. Cancer Res 2006;66:3214-21.
-
(2006)
Cancer Res
, vol.66
, pp. 3214-3221
-
-
Kovtun, Y.V.1
Audette, C.A.2
Ye, Y.3
Xie, H.4
Ruberti, M.F.5
Phinney, S.J.6
-
28
-
-
76049122850
-
Intracellular activation of SGN-35, a potent anti-CD30 antibodydrug conjugate
-
Okeley NM, Miyamoto JB, Zhang X, Sanderson RJ, Benjamin DR, Sievers EL, et al. Intracellular activation of SGN-35, a potent anti-CD30 antibodydrug conjugate. Clin Cancer Res 2010;16:888-97.
-
(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
-
29
-
-
84942085714
-
IMGN853, a folate receptor-alpha (FRalpha)-targeting antibody-drug conjugate, exhibits potent targeted antitumor activity against FRalpha-expressing tumors
-
Ab O, Whiteman KR, Bartle LM, Sun X, Singh R, Tavares D, et al. IMGN853, a folate receptor-alpha (FRalpha)-targeting antibody-drug conjugate, exhibits potent targeted antitumor activity against FRalpha-expressing tumors. Mol Cancer Ther 2015;14:1605-13.
-
(2015)
Mol Cancer Ther
, vol.14
, pp. 1605-1613
-
-
Ab, O.1
Whiteman, K.R.2
Bartle, L.M.3
Sun, X.4
Singh, R.5
Tavares, D.6
-
30
-
-
84856373074
-
Synthesis and biological evaluation of antibody conjugates of phosphate prodrugs of cytotoxic DNA alkylators for the targeted treatment of cancer
-
Zhao RY, Erickson HK, Leece BA, Reid EE, Goldmacher VS, Lambert JM, et al. Synthesis and biological evaluation of antibody conjugates of phosphate prodrugs of cytotoxic DNA alkylators for the targeted treatment of cancer. J Med Chem 2012;55:766-82.
-
(2012)
J Med Chem
, vol.55
, pp. 766-782
-
-
Zhao, R.Y.1
Erickson, H.K.2
Leece, B.A.3
Reid, E.E.4
Goldmacher, V.S.5
Lambert, J.M.6
-
31
-
-
84954072873
-
First-in-human multicenter phase I study of BMS-936561 (MDX-1203), an antibody-drug conjugate targeting CD70
-
Owonikoko TK, Hussain A, Stadler WM, Smith DC, Kluger H, Molina AM, et al. First-in-human multicenter phase I study of BMS-936561 (MDX-1203), an antibody-drug conjugate targeting CD70. Cancer Chemother Pharmacol 2016;77:155-62.
-
(2016)
Cancer Chemother Pharmacol
, vol.77
, pp. 155-162
-
-
Owonikoko, T.K.1
Hussain, A.2
Stadler, W.M.3
Smith, D.C.4
Kluger, H.5
Molina, A.M.6
-
32
-
-
84940839864
-
The preclinical profile of the duocarmycin-based HER2-targeting ADC SYD985 predicts for clinical benefit in low HER2-expressing breast cancers
-
van der Lee MM, Groothuis PG, Ubink R, van der Vleuten MA, van Achterberg TA, Loosveld EM, et al. The preclinical profile of the duocarmycin-based HER2-targeting ADC SYD985 predicts for clinical benefit in low HER2-expressing breast cancers. Mol Cancer Ther 2015;14:692-703.
-
(2015)
Mol Cancer Ther
, vol.14
, pp. 692-703
-
-
Van Der, L.M.M.1
Groothuis, P.G.2
Ubink, R.3
Van Der, V.Ma.4
Van Achterberg, T.A.5
Loosveld, E.M.6
Et, A.7
-
33
-
-
0013909023
-
Quantitative comparison of toxicity of anticancer agents in mouse, rat, hamster, dog, monkey, and man
-
Freireich EJ, Gehan EA, Rall DP, Schmidt LH, Skipper HE. Quantitative comparison of toxicity of anticancer agents in mouse, rat, hamster, dog, monkey, and man. Cancer Chemother Rep 1966;50:219-44.
-
(1966)
Cancer Chemother Rep
, vol.50
, pp. 219-244
-
-
Freireich, E.J.1
Gehan, E.A.2
Rall, D.P.3
Schmidt, L.H.4
Skipper, H.E.5
-
34
-
-
79955022475
-
Disulfidelinked antibody-maytansinoid conjugates: Optimization of in vivo activity by varying the steric hindrance at carbon atoms adjacent to the disulfide linkage
-
Kellogg BA, Garrett L, Kovtun Y, Lai KC, Leece B, Miller M, et al. Disulfidelinked antibody-maytansinoid conjugates: optimization of in vivo activity by varying the steric hindrance at carbon atoms adjacent to the disulfide linkage. Bioconjug Chem 2011;22:717-27.
-
(2011)
Bioconjug Chem
, vol.22
, pp. 717-727
-
-
Kellogg, B.A.1
Garrett, L.2
Kovtun, Y.3
Lai, K.C.4
Leece, B.5
Miller, M.6
-
35
-
-
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, et al. Enhanced activity of monomethylauristatin F through monoclonal antibody delivery: effects of linker technology on efficacy and toxicity. Bioconjug Chem 2006;17:114-24.
-
(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
|