Bates SE - Search Results

1

Toward individualized treatment: prediction of anticancer drug disposition and toxicity with pharmacogenetics.

Deeken JF, Figg WD, Bates SE, Sparreboom A. Deeken JF, et al. Among authors: bates se. Anticancer Drugs. 2007 Feb;18(2):111-26. doi: 10.1097/CAD.0b013e3280109411. Anticancer Drugs. 2007. PMID: 17159598 Review.

2

Initial pharmacokinetics and bioavailability of PSC 833, a P-glycoprotein antagonist.

Lush RM, Meadows B, Fojo AT, Kalafsky G, Smith HT, Bates S, Figg WD. Lush RM, et al. J Clin Pharmacol. 1997 Feb;37(2):123-8. doi: 10.1002/j.1552-4604.1997.tb04770.x. J Clin Pharmacol. 1997. PMID: 9055138 Clinical Trial.

3

FR901228 causes mitotic arrest but does not alter microtubule polymerization.

Sandor V, Robbins AR, Robey R, Myers T, Sausville E, Bates SE, Sackett DL. Sandor V, et al. Among authors: bates se. Anticancer Drugs. 2000 Jul;11(6):445-54. doi: 10.1097/00001813-200007000-00005. Anticancer Drugs. 2000. PMID: 11001385

4

Phase I study of infusional paclitaxel in combination with the P-glycoprotein antagonist PSC 833.

Chico I, Kang MH, Bergan R, Abraham J, Bakke S, Meadows B, Rutt A, Robey R, Choyke P, Merino M, Goldspiel B, Smith T, Steinberg S, Figg WD, Fojo T, Bates S. Chico I, et al. J Clin Oncol. 2001 Feb 1;19(3):832-42. doi: 10.1200/JCO.2001.19.3.832. J Clin Oncol. 2001. PMID: 11157037 Clinical Trial.

5

The P-glycoprotein antagonist PSC 833 increases the plasma concentrations of 6alpha-hydroxypaclitaxel, a major metabolite of paclitaxel.

Kang MH, Figg WD, Ando Y, Blagosklonny MV, Liewehr D, Fojo T, Bates SE. Kang MH, et al. Among authors: bates se. Clin Cancer Res. 2001 Jun;7(6):1610-7. Clin Cancer Res. 2001. PMID: 11410497 Clinical Trial.

6

A Phase I study of infusional vinblastine in combination with the P-glycoprotein antagonist PSC 833 (valspodar).

Bates S, Kang M, Meadows B, Bakke S, Choyke P, Merino M, Goldspiel B, Chico I, Smith T, Chen C, Robey R, Bergan R, Figg WD, Fojo T. Bates S, et al. Cancer. 2001 Sep 15;92(6):1577-90. doi: 10.1002/1097-0142(20010915)92:6<1577::aid-cncr1484>3.0.co;2-h. Cancer. 2001. PMID: 11745237 Clinical Trial.

7

Phase I trial of the histone deacetylase inhibitor, depsipeptide (FR901228, NSC 630176), in patients with refractory neoplasms.

Sandor V, Bakke S, Robey RW, Kang MH, Blagosklonny MV, Bender J, Brooks R, Piekarz RL, Tucker E, Figg WD, Chan KK, Goldspiel B, Fojo AT, Balcerzak SP, Bates SE. Sandor V, et al. Among authors: bates se. Clin Cancer Res. 2002 Mar;8(3):718-28. Clin Cancer Res. 2002. PMID: 11895901 Clinical Trial.

8

A phase I/II study of infusional vinblastine with the P-glycoprotein antagonist valspodar (PSC 833) in renal cell carcinoma.

Bates SE, Bakke S, Kang M, Robey RW, Zhai S, Thambi P, Chen CC, Patil S, Smith T, Steinberg SM, Merino M, Goldspiel B, Meadows B, Stein WD, Choyke P, Balis F, Figg WD, Fojo T. Bates SE, et al. Clin Cancer Res. 2004 Jul 15;10(14):4724-33. doi: 10.1158/1078-0432.CCR-0829-03. Clin Cancer Res. 2004. PMID: 15269145 Clinical Trial.

9

Determination of the cyclic depsipeptide FK228, a histone deacetylase inhibitor, by liquid chromatography-mass spectrometry.

Hwang K, Piekarz RL, Bates SE, Figg WD, Sparreboom A. Hwang K, et al. Among authors: bates se. J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Sep 25;809(1):81-6. doi: 10.1016/j.jchromb.2004.06.007. J Chromatogr B Analyt Technol Biomed Life Sci. 2004. PMID: 15282096

10

Effect of common CYP3A4 and CYP3A5 variants on the pharmacokinetics of the cytochrome P450 3A phenotyping probe midazolam in cancer patients.

Lepper ER, Baker SD, Permenter M, Ries N, van Schaik RH, Schenk PW, Price DK, Ahn D, Smith NF, Cusatis G, Ingersoll RG, Bates SE, Mathijssen RH, Verweij J, Figg WD, Sparreboom A. Lepper ER, et al. Among authors: bates se. Clin Cancer Res. 2005 Oct 15;11(20):7398-404. doi: 10.1158/1078-0432.CCR-05-0520. Clin Cancer Res. 2005. PMID: 16243813 Clinical Trial.

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