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Volumn 71, Issue 1, 2013, Pages 133-143

PK-PD modeling of combination efficacy effect from administration of the MEK inhibitor GDC-0973 and PI3K inhibitor GDC-0941 in A2058 xenografts

Author keywords

A2058 tumor; MEK inhibitor; Pharmacokinetic pharmacodynamic modeling; PI3K inhibitor; Tumor xenograft

Indexed keywords

ANTINEOPLASTIC AGENT; GDC 0973; PICTILISIB; UNCLASSIFIED DRUG;

EID: 84872325988     PISSN: 03445704     EISSN: 14320843     Source Type: Journal    
DOI: 10.1007/s00280-012-1988-6     Document Type: Article
Times cited : (29)

References (38)
  • 1
    • 0032443803 scopus 로고    scopus 로고
    • The akt kinase: Molecular determinants of oncogenicity
    • 9843996 10.1073/pnas.95.25.14950 1:CAS:528:DyaK1cXotVGlsrw%3D
    • Aoki M, Batista O, Bellacosa A, Tsichlis P, Vogt PK (1998) The akt kinase: molecular determinants of oncogenicity. Proc Natl Acad Sci USA 95:14950-14955
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 14950-14955
    • Aoki, M.1    Batista, O.2    Bellacosa, A.3    Tsichlis, P.4    Vogt, P.K.5
  • 2
    • 78651385352 scopus 로고    scopus 로고
    • A dual PI3K/mTOR inhibitor, PI-103, cooperates with stem cell-delivered TRAIL in experimental glioma models
    • 21084267 10.1158/0008-5472.CAN-10-1601 1:CAS:528:DC%2BC3MXovFKg
    • Bagci-Onder T, Wakimoto H, Anderegg M, Cameron C, Shah K (2011) A dual PI3K/mTOR inhibitor, PI-103, cooperates with stem cell-delivered TRAIL in experimental glioma models. Cancer Res 71:154-163
    • (2011) Cancer Res , vol.71 , pp. 154-163
    • Bagci-Onder, T.1    Wakimoto, H.2    Anderegg, M.3    Cameron, C.4    Shah, K.5
  • 6
    • 0021118703 scopus 로고
    • Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
    • 6382953 10.1016/0065-2571(84)90007-4 1:CAS:528:DyaL2cXktlaksLk%3D
    • Chou TC, Talalay P (1984) Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv Enzyme Regul 22:27-55
    • (1984) Adv Enzyme Regul , vol.22 , pp. 27-55
    • Chou, T.C.1    Talalay, P.2
  • 7
    • 70350034197 scopus 로고    scopus 로고
    • Contemporary pre-clinical development of anticancer agents-what are the optimal preclinical models?
    • 19762228 10.1016/j.ejca.2009.08.008 1:CAS:528:DC%2BD1MXhtlSqsLzE
    • Damia G, D'Incalci M (2009) Contemporary pre-clinical development of anticancer agents-what are the optimal preclinical models? Eur J Cancer 45:2768-2781
    • (2009) Eur J Cancer , vol.45 , pp. 2768-2781
    • Damia, G.1    D'Incalci, M.2
  • 8
    • 76249092302 scopus 로고    scopus 로고
    • Isoform-specific phosphoinositide 3-kinase inhibitors exert distinct effects in solid tumors
    • 20103642 10.1158/0008-5472.CAN-09-2525 1:CAS:528:DC%2BC3cXht12ruro%3D
    • Edgar KA, Wallin JJ, Berry M, Lee LB, Prior WW, Sampath D, Friedman LS, Belvin M (2010) Isoform-specific phosphoinositide 3-kinase inhibitors exert distinct effects in solid tumors. Cancer Res 70:1164-1172
    • (2010) Cancer Res , vol.70 , pp. 1164-1172
    • Edgar, K.A.1    Wallin, J.J.2    Berry, M.3    Lee, L.B.4    Prior, W.W.5    Sampath, D.6    Friedman, L.S.7    Belvin, M.8
  • 10
    • 33746565515 scopus 로고    scopus 로고
    • Role of Raf kinase in cancer: Therapeutic potential of targeting the Raf/MEK/ERK signal transduction pathway
    • 16890795 10.1053/j.seminoncol.2006.04.002 1:CAS:528:DC%2BD28XpsVersLc%3D
    • Gollob JA, Wilhelm S, Carter C, Kelley SL (2006) Role of Raf kinase in cancer: therapeutic potential of targeting the Raf/MEK/ERK signal transduction pathway. Semin Oncol 33:392-406
    • (2006) Semin Oncol , vol.33 , pp. 392-406
    • Gollob, J.A.1    Wilhelm, S.2    Carter, C.3    Kelley, S.L.4
  • 12
    • 0029036955 scopus 로고
    • The search for synergy: A critical review from a response surface perspective
    • 7568331 1:STN:280:DyaK28%2FjsFSgtQ%3D%3D
    • Greco WR, Bravo G, Parsons JC (1995) The search for synergy: a critical review from a response surface perspective. Pharmacol Rev 47:331-385
    • (1995) Pharmacol Rev , vol.47 , pp. 331-385
    • Greco, W.R.1    Bravo, G.2    Parsons, J.C.3
  • 15
    • 67349159357 scopus 로고    scopus 로고
    • Modeling of tumor growth and anticancer effects of combination therapy
    • 19387803 10.1007/s10928-009-9117-9 1:CAS:528:DC%2BD1MXltl2gu78%3D
    • Koch G, Walz A, Lahu G, Schropp J (2009) Modeling of tumor growth and anticancer effects of combination therapy. J Pharmacokinet Pharmacodyn 36:179-197
    • (2009) J Pharmacokinet Pharmacodyn , vol.36 , pp. 179-197
    • Koch, G.1    Walz, A.2    Lahu, G.3    Schropp, J.4
  • 17
    • 39149133664 scopus 로고    scopus 로고
    • Is B-Raf a good therapeutic target for melanoma and other malignancies?
    • 18172288 10.1158/0008-5472.CAN-07-2038 1:CAS:528:DC%2BD1cXoslag
    • Madhunapantula SV, Robertson GP (2008) Is B-Raf a good therapeutic target for melanoma and other malignancies? Cancer Res 68:5-8
    • (2008) Cancer Res , vol.68 , pp. 5-8
    • Madhunapantula, S.V.1    Robertson, G.P.2
  • 18
    • 67649312041 scopus 로고    scopus 로고
    • Scaling pharmacodynamics from in vitro and preclinical animal studies to humans
    • 19252333 10.2133/dmpk.24.16 1:CAS:528:DC%2BD1MXks1Whu78%3D
    • Mager DE, Woo S, Jusko WJ (2009) Scaling pharmacodynamics from in vitro and preclinical animal studies to humans. Drug Metab Pharmacokinet 24:16-24
    • (2009) Drug Metab Pharmacokinet , vol.24 , pp. 16-24
    • Mager, D.E.1    Woo, S.2    Jusko, W.J.3
  • 20
    • 23744475396 scopus 로고    scopus 로고
    • Pharmacokinetic-pharmacodynamic-efficacy analysis of efalizumab in patients with moderate to severe psoriasis
    • 16028009 10.1007/s11095-005-5642-4 1:CAS:528:DC%2BD2MXmt1yntbw%3D
    • Ng CM, Joshi A, Dedrick RL, Garovoy MR, Bauer RJ (2005) Pharmacokinetic-pharmacodynamic-efficacy analysis of efalizumab in patients with moderate to severe psoriasis. Pharm Res 22:1088-1100
    • (2005) Pharm Res , vol.22 , pp. 1088-1100
    • Ng, C.M.1    Joshi, A.2    Dedrick, R.L.3    Garovoy, M.R.4    Bauer, R.J.5
  • 23
    • 70450250213 scopus 로고    scopus 로고
    • Testing additivity of anticancer agents in pre-clinical studies: A PK/PD modelling approach
    • 19854637 10.1016/j.ejca.2009.09.025 1:CAS:528:DC%2BD1MXhsVyms7fJ
    • Rocchetti M, Del Bene F, Germani M, Fiorentini F, Poggesi I, Pesenti E, Magni P, De Nicolao G (2009) Testing additivity of anticancer agents in pre-clinical studies: a PK/PD modelling approach. Eur J Cancer 45:3336-3346
    • (2009) Eur J Cancer , vol.45 , pp. 3336-3346
    • Rocchetti, M.1    Del Bene, F.2    Germani, M.3    Fiorentini, F.4    Poggesi, I.5    Pesenti, E.6    Magni, P.7    De Nicolao, G.8
  • 24
    • 77955986074 scopus 로고    scopus 로고
    • Pharmacokinetic-pharmacodynamic modeling of tumor growth inhibition and biomarker modulation by the novel phosphatidylinositol 3-kinase inhibitor GDC-0941
    • 20538720 10.1124/dmd.110.032912 1:CAS:528:DC%2BC3cXhtFegu7zN
    • Salphati L, Wong H, Belvin M, Bradford D, Edgar KA, Prior WW, Sampath D, Wallin JJ (2010) Pharmacokinetic-pharmacodynamic modeling of tumor growth inhibition and biomarker modulation by the novel phosphatidylinositol 3-kinase inhibitor GDC-0941. Drug Metab Dispos 38:1436-1442
    • (2010) Drug Metab Dispos , vol.38 , pp. 1436-1442
    • Salphati, L.1    Wong, H.2    Belvin, M.3    Bradford, D.4    Edgar, K.A.5    Prior, W.W.6    Sampath, D.7    Wallin, J.J.8
  • 27
    • 33645734205 scopus 로고    scopus 로고
    • Contributions of human tumor xenografts to anticancer drug development
    • discussion 3354
    • Sausville EA, Burger AM (2006) Contributions of human tumor xenografts to anticancer drug development. Cancer Res 66: 3351-3354, discussion 3354
    • (2006) Cancer Res , vol.66 , pp. 3351-3354
    • Sausville, E.A.1    Burger, A.M.2
  • 28
    • 33749635119 scopus 로고    scopus 로고
    • Raf kinases: Oncogenesis and drug discovery
    • Schreck R, Rapp UR (2006) Raf kinases: Oncogenesis and drug discovery. Int J Cancer 119:2261-2271
    • (2006) Int J Cancer , vol.119 , pp. 2261-2271
    • Schreck, R.1    Rapp, U.R.2
  • 29
    • 10344258041 scopus 로고    scopus 로고
    • Targeting the mitogen-activated protein kinase cascade to treat cancer
    • 15573115 10.1038/nrc1503 1:CAS:528:DC%2BD2cXhtVarsLjO
    • Sebolt-Leopold JS, Herrera R (2004) Targeting the mitogen-activated protein kinase cascade to treat cancer. Nat Rev Cancer 4:937-947
    • (2004) Nat Rev Cancer , vol.4 , pp. 937-947
    • Sebolt-Leopold, J.S.1    Herrera, R.2
  • 31
    • 0001582482 scopus 로고
    • Molecular cloning of the akt oncogene and its human homologues AKT1 and AKT2: Amplification of AKT1 in a primary human gastric adenocarcinoma
    • 3037531 10.1073/pnas.84.14.5034 1:CAS:528:DyaL2sXkvFWhtb8%3D
    • Staal SP (1987) Molecular cloning of the akt oncogene and its human homologues AKT1 and AKT2: amplification of AKT1 in a primary human gastric adenocarcinoma. Proc Natl Acad Sci USA 84:5034-5037
    • (1987) Proc Natl Acad Sci USA , vol.84 , pp. 5034-5037
    • Staal, S.P.1
  • 33
    • 33750435151 scopus 로고    scopus 로고
    • Tumor models for efficacy determination
    • 17041086 10.1158/1535-7163.MCT-06-0391 1:CAS:528:DC%2BD28XhtVOmtbbJ
    • Teicher BA (2006) Tumor models for efficacy determination. Mol Cancer Ther 5:2435-2443
    • (2006) Mol Cancer Ther , vol.5 , pp. 2435-2443
    • Teicher, B.A.1
  • 34
    • 39749131036 scopus 로고    scopus 로고
    • Preclinical pharmacokinetic/pharmacodynamic models of gefitinib and the design of equivalent dosing regimens in EGFR wild-type and mutant tumor models
    • 18281523 10.1158/1535-7163.MCT-07-2070
    • Wang S, Guo P, Wang X, Zhou Q, Gallo JM (2008) Preclinical pharmacokinetic/pharmacodynamic models of gefitinib and the design of equivalent dosing regimens in EGFR wild-type and mutant tumor models. Mol Cancer Ther 7:407-417
    • (2008) Mol Cancer Ther , vol.7 , pp. 407-417
    • Wang, S.1    Guo, P.2    Wang, X.3    Zhou, Q.4    Gallo, J.M.5
  • 35
    • 67649344800 scopus 로고    scopus 로고
    • Demonstration of the equivalent pharmacokinetic/pharmacodynamic dosing strategy in a multiple-dose study of gefitinib
    • 19509243 10.1158/1535-7163.MCT-09-0089 1:CAS:528:DC%2BD1MXntVKgsLY%3D
    • Wang S, Zhou Q, Gallo JM (2009) Demonstration of the equivalent pharmacokinetic/pharmacodynamic dosing strategy in a multiple-dose study 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
  • 36
    • 63849122381 scopus 로고    scopus 로고
    • Pharmacodynamics of 2-[4-[(1E)-1-(hydroxyimino)-2,3-dihydro-1H-inden-5- yl]-3-(pyridine-4-yl)-1 H-pyrazol-1-yl]ethan-1-ol (GDC-0879), a potent and selective B-Raf kinase inhibitor: Understanding relationships between systemic concentrations, phosphorylated mitogen-activated protein kinase kinase 1 inhibition, and efficacy
    • 19147858 10.1124/jpet.108.148189 1:CAS:528:DC%2BD1MXksVKmsrY%3D
    • Wong H, Belvin M, Herter S, Hoeflich KP, Murray LJ, Wong L, Choo EF (2009) Pharmacodynamics of 2-[4-[(1E)-1-(hydroxyimino)-2,3-dihydro-1H-inden-5- yl]-3-(pyridine-4-yl)-1 H-pyrazol-1-yl]ethan-1-ol (GDC-0879), a potent and selective B-Raf kinase inhibitor: understanding relationships between systemic concentrations, phosphorylated mitogen-activated protein kinase kinase 1 inhibition, and efficacy. J Pharmacol Exp Ther 329:360-367
    • (2009) J Pharmacol Exp Ther , vol.329 , pp. 360-367
    • Wong, H.1    Belvin, M.2    Herter, S.3    Hoeflich, K.P.4    Murray, L.J.5    Wong, L.6    Choo, E.F.7
  • 38
    • 33745327045 scopus 로고    scopus 로고
    • Back to the roots: The remarkable RAF oncogene story
    • 16649144 10.1007/s00018-006-6005-y 1:CAS:528:DC%2BD28Xmslaisbk%3D
    • Zebisch A, Troppmair J (2006) Back to the roots: the remarkable RAF oncogene story. Cell Mol Life Sci 63:1314-1330
    • (2006) Cell Mol Life Sci , vol.63 , pp. 1314-1330
    • Zebisch, A.1    Troppmair, J.2


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