Population Pharmacokinetics of CCI‐779: Correlations to Safety and Pharmacogenomic Responses in Patients with Advanced Renal Cancer
暂无分享,去创建一个
A. Dorner | J. Boni | M. Burczynski | N. Twine | F. Immermann | Michael E Burczynski | Jennifer A Stover | C. Leister | G. Bender | V. Fitzpatrick | Joseph P Boni | Cathie Leister | Gregor Bender | Virginia Fitzpatrick | Natalie Twine | Jennifer Stover | Andrew Dorner | Fred Immermann | Michael E. Burczynski | J. Stover | Joseph P. Boni
[1] C. Meisel,et al. Frequency of single nucleotide polymorphisms in the P‐glycoprotein drug transporter MDR1 gene in white subjects , 2001, Clinical pharmacology and therapeutics.
[2] D. Goldstein,et al. Association of multidrug resistance in epilepsy with a polymorphism in the drug-transporter gene ABCB1. , 2003, The New England journal of medicine.
[3] B. Geoerger,et al. Antitumor activity of the rapamycin analog CCI-779 in human primitive neuroectodermal tumor/medulloblastoma models as single agent and in combination chemotherapy. , 2001, Cancer research.
[4] M. Tyers,et al. Molecular profiling of non-small cell lung cancer and correlation with disease-free survival. , 2002, Cancer research.
[5] P. Vogt. PI 3-kinase, mTOR, protein synthesis and cancer. , 2001, Trends in molecular medicine.
[6] D. DuBois,et al. A formula to estimate the approximate surface area if height and weight be known , 1989 .
[7] K. Nakayama,et al. Human MDR1 polymorphism: G2677T/A and C3435T have no effect on MDR1 transport activities. , 2003, Biochemical pharmacology.
[8] P. Frost,et al. mTOR, a novel target in breast cancer: the effect of CCI-779, an mTOR inhibitor, in preclinical models of breast cancer. , 2001, Endocrine-related cancer.
[9] P. Hedrick,et al. Gametic disequilibrium measures: proceed with caution. , 1987, Genetics.
[10] E. Schuetz,et al. Co-regulation of CYP3A4 and CYP3A5 and contribution to hepatic and intestinal midazolam metabolism. , 2002, Molecular pharmacology.
[11] F. Valentine,et al. Population Pharmacokinetic Analysis of Didanosine (2′,3′‐Dideoxyinosine) Plasma Concentrations Obtained in Phase I Clinical Trials in Patients with AIDS or AIDS‐Related Complex , 1992, Journal of clinical pharmacology.
[12] Manuel Hidalgo,et al. Disease-associated expression profiles in peripheral blood mononuclear cells from patients with advanced renal cell carcinoma. , 2003, Cancer research.
[13] M. Relling,et al. Conventional compared with individualized chemotherapy for childhood acute lymphoblastic leukemia. , 1998, The New England journal of medicine.
[14] S. Krawetz,et al. Surrogate tissue analysis: monitoring toxicant exposure and health status of inaccessible tissues through the analysis of accessible tissues and cells. , 2004, Toxicology and applied pharmacology.
[15] Hong Wu,et al. Enhanced sensitivity of PTEN-deficient tumors to inhibition of FRAP/mTOR , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[16] Yudong D. He,et al. Gene expression profiling predicts clinical outcome of breast cancer , 2002, Nature.
[17] U. Christians,et al. Metabolism and transport of the macrolide immunosuppressant sirolimus in the small intestine. , 1998, The Journal of pharmacology and experimental therapeutics.
[18] M. Gottesman,et al. Multidrug resistance in cancer: role of ATP–dependent transporters , 2002, Nature Reviews Cancer.
[19] B. Holman,et al. In vivo metabolism of the technetium isonitrile complex [Tc(2-ethoxy-2-methyl-1-isocyanopropane)6]+. , 1994, Nuclear medicine and biology.
[20] T. Fojo,et al. Increased 99mTc-sestamibi accumulation in normal liver and drug-resistant tumors after the administration of the glycoprotein inhibitor, XR9576. , 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.
[21] Christopher J. Palestro,et al. Sestamibi is a substrate for MDR1 and MDR2 P-glycoprotein genes , 2003, European Journal of Nuclear Medicine and Molecular Imaging.
[22] W. Haefeli,et al. Inhibition of P-Glycoprotein by Newer Antidepressants , 2003, Journal of Pharmacology and Experimental Therapeutics.
[23] U. Christians,et al. Cytochrome P-450 3A enzymes are responsible for biotransformation of FK506 and rapamycin in man and rat. , 1992, Drug metabolism and disposition: the biological fate of chemicals.
[24] U. Hofmann,et al. MDR1 gene polymorphisms and disposition of the P-glycoprotein substrate fexofenadine. , 2002, British journal of clinical pharmacology.
[25] J. Kronauge,et al. Uptake and retention of hexakis (2-methoxyisobutyl isonitrile) technetium(I) in cultured chick myocardial cells. Mitochondrial and plasma membrane potential dependence. , 1990, Circulation.
[26] D. Lockhart,et al. Expression monitoring by hybridization to high-density oligonucleotide arrays , 1996, Nature Biotechnology.
[27] M. Fromm. The influence of MDR1 polymorphisms on P-glycoprotein expression and function in humans. , 2002, Advanced drug delivery reviews.
[28] U. Brinkmann,et al. The predictive value of MDR1, CYP2C9, and CYP2C19 polymorphisms for phenytoin plasma levels , 2001, The Pharmacogenomics Journal.
[29] J. Bergh,et al. Tailored fluorouracil, epirubicin, and cyclophosphamide compared with marrow-supported high-dose chemotherapy as adjuvant treatment for high-risk breast cancer: a randomised trial , 2000, The Lancet.
[30] B. Swanson. Delivery of High-Quality Biomarker Assays , 2002, Disease markers.
[31] E. Franssen,et al. Visualization of multidrug resistance in vivo , 1999, European Journal of Nuclear Medicine.
[32] H. McLeod,et al. MDR1 pharmacogenetics: frequency of the C3435T mutation in exon 26 is significantly influenced by ethnicity. , 2001, Pharmacogenetics.
[33] R. Kim,et al. Coordinate induction of both cytochrome P4503A and MDR1 by St John's wort in healthy subjects , 2003, Clinical pharmacology and therapeutics.
[34] K Püschel,et al. Standard liver volume in the Caucasian population. , 1999, Liver transplantation and surgery : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.
[35] S. Kawasaki,et al. Calculation of child and adult standard liver volume for liver transplantation , 1995, Hepatology.
[36] E. Sausville,et al. Biochemical correlates of mTOR inhibition by the rapamycin ester CCI-779 and tumor growth inhibition. , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.
[37] J. Dobkin,et al. Modulation of the multidrug resistance P-glycoprotein: detection with technetium-99m-sestamibi in vivo. , 1997, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.
[38] C. Clarke,et al. CYP3A5 Genotype and Midazolam Clearance in Australian Patients Receiving Chemotherapy , 2004, Clinical pharmacology and therapeutics.
[39] S. Uemoto,et al. C3435T polymorphism in the MDR1 gene affects the enterocyte expression level of CYP3A4 rather than Pgp in recipients of living-donor liver transplantation. , 2002, Pharmacogenetics.
[40] B. Goh,et al. Explaining interindividual variability of docetaxel pharmacokinetics and pharmacodynamics in Asians through phenotyping and genotyping strategies. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[41] M. Kasuga,et al. Effect of the mutation (C3435T) at exon 26 of the MDR1 gene on expression level of MDR1 messenger ribonucleic acid in duodenal enterocytes of healthy Japanese subjects , 2002, Clinical pharmacology and therapeutics.
[42] D. Slonim,et al. Evaluation of normalization procedures for oligonucleotide array data based on spiked cRNA controls , 2001, Genome Biology.
[43] H. Kroemer,et al. Effect of levothyroxine administration on intestinal P‐glycoprotein expression: Consequences for drug disposition * , 2002, Clinical pharmacology and therapeutics.
[44] Jacques Fellay,et al. Response to antiretroviral treatment in HIV-1-infected individuals with allelic variants of the multidrug resistance transporter 1: a pharmacogenetics study , 2002, The Lancet.
[45] E. de Vries,et al. Comparison of the kinetics of active efflux of 99mTc-MIBI in cells with P-glycoprotein-mediated and multidrug-resistance protein-associated multidrug-resistance phenotypes. , 1998, European journal of biochemistry.
[46] H. Gurney,et al. Dose calculation of anticancer drugs: a review of the current practice and introduction of an alternative. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[47] D. Sloane,et al. An Introduction to Categorical Data Analysis , 1996 .
[48] E. Schuetz,et al. Interaction of Cytochrome P450 3A Inhibitors with P-Glycoprotein , 2002, Journal of Pharmacology and Experimental Therapeutics.
[49] R. Kim,et al. Identification of functionally variant MDR1 alleles among European Americans and African Americans , 2001, Clinical pharmacology and therapeutics.
[50] E. Ette,et al. Stability and Performance of a Population Pharmacokinetic Model , 1997, Journal of clinical pharmacology.
[51] C. Punt,et al. Phase I and pharmacokinetic study of CCI-779, a novel cytostatic cell-cycle inhibitor, in combination with 5-fluorouracil and leucovorin in patients with advanced solid tumors. , 2003, Annals of oncology : official journal of the European Society for Medical Oncology.
[52] M. Matarrese,et al. Biodistribution of Tc-99m methoxy-isobutyl-isonitrile (MIBI) in humans , 2004, European Journal of Nuclear Medicine.
[53] R. Bookstein,et al. Mutations to CCI-779 PTEN Enhanced Sensitivity of Multiple Myeloma Cells Containing Updated Version , 2002 .
[54] E. B. Cunningham. An inositolphosphate-binding immunophilin, IPBP12. , 1999, Blood.
[55] M. Kasuga,et al. Interaction of Docetaxel (“Taxotere”) with Human P‐Glycoprotein , 1999, Japanese journal of cancer research : Gann.
[56] N H Holford,et al. A procedure for generating bootstrap samples for the validation of nonlinear mixed-effects population models. , 1999, Computer methods and programs in biomedicine.
[57] Emanuel F. Petricoin,et al. Medical applications of microarray technologies: a regulatory science perspective , 2002, Nature Genetics.
[58] U. Brinkmann,et al. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[59] J. Gorski,et al. Induction of multidrug resistance-1 and cytochrome P450 mRNAs in human mononuclear cells by rifampin. , 2002, Drug metabolism and disposition: the biological fate of chemicals.