Search Results - "Holleran, Julianne"
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NCI Comparative Oncology Program Testing of Non-Camptothecin Indenoisoquinoline Topoisomerase I Inhibitors in Naturally Occurring Canine Lymphoma
Published in Clinical cancer research (01-12-2018)“…Only one chemical class of topoisomerase I (TOP1) inhibitors is FDA approved, the camptothecins with irinotecan and topotecan widely used. Because of their…”
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Phase I Study of Vorinostat in Combination with Bortezomib for Relapsed and Refractory Multiple Myeloma
Published in Clinical cancer research (15-08-2009)“…Purpose: Vorinostat, a histone deacetylase inhibitor, enhances cell death by the proteasome inhibitor bortezomib in vitro . We sought to test the combination…”
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Evaluating the indotecan-neutropenia relationship in patients with solid tumors by population pharmacokinetic modeling and sigmoidal E max regressions
Published in Cancer chemotherapy and pharmacology (01-03-2023)“…This study aimed at characterizing indotecan population pharmacokinetics and explore the indotecan-neutropenia relationship in patients with solid tumors…”
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Evaluating the indotecan–neutropenia relationship in patients with solid tumors by population pharmacokinetic modeling and sigmoidal Emax regressions
Published in Cancer chemotherapy and pharmacology (01-03-2023)“…Purpose This study aimed at characterizing indotecan population pharmacokinetics and explore the indotecan–neutropenia relationship in patients with solid…”
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Quantitation of tazemetostat in human plasma using liquid chromatography–tandem mass spectrometry
Published in Biomedical chromatography (01-07-2024)“…To support a phase 1 trial in patients with lymphomas, we developed a liquid chromatography–tandem mass spectrometry (LC–MS/MS) method for tazemetostat…”
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Simultaneous quantitation of abiraterone, enzalutamide, N-desmethyl enzalutamide, and bicalutamide in human plasma by LC–MS/MS
Published in Journal of pharmaceutical and biomedical analysis (10-05-2017)“…[Display omitted] •Bicalutamide, enzalutamide and abiraterone target the androgen receptor pathway.•A phase 3 trial of enzalutamide and abiraterone in…”
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Dexamethasone to prevent everolimus-induced stomatitis (Alliance MIST Trial: A221701)
Published in Seminars in oncology (01-02-2023)“…mTOR inhibitors such as everolimus may cause oral stomatitis, often a dose-limiting toxicity. Prior clinical research has suggested that a dexamethasone mouth…”
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Phase I Pharmacokinetic and Pharmacodynamic Study of 17-dimethylaminoethylamino-17-demethoxygeldanamycin, an Inhibitor of Heat-Shock Protein 90, in Patients With Advanced Solid Tumors
Published in Journal of clinical oncology (20-03-2010)“…To define the maximum tolerated dose, toxicities, pharmacokinetics, and pharmacodynamics of 17-dimethylaminoethylamino-17-demethoxygeldanamycin (17DMAG)…”
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Quantitation of iohexol, a glomerular filtration marker, in human plasma by LC–MS/MS
Published in Journal of pharmaceutical and biomedical analysis (10-09-2020)“…•Iohexol is a widely used marker for measuring glomerular filtration rate (GFR).•Accurate GFR measurement is important in treatment decisions in oncology.•We…”
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Evaluation of the pharmacokinetic drug-drug interaction potential of iohexol, a renal filtration marker
Published in Cancer chemotherapy and pharmacology (01-10-2020)“…Purpose Carboplatin dose is calculated based on kidney function, commonly estimated with imperfect creatinine-based formulae. Iohexol is used to measure…”
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Phase I Study of Decitabine in Combination with Vorinostat in Patients with Advanced Solid Tumors and Non-Hodgkin's Lymphomas
Published in Clinical cancer research (15-03-2011)“…This phase I study evaluated the safety, tolerability, pharmacokinetics, and preliminary efficacy of the combination of decitabine with vorinostat. Patients…”
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Phase I Study of Vorinostat in Patients With Advanced Solid Tumors and Hepatic Dysfunction: A National Cancer Institute Organ Dysfunction Working Group Study
Published in Journal of clinical oncology (10-10-2010)“…Vorinostat is the first US Food and Drug Administration-approved histone deacetylase inhibitor and is indicated for the treatment of refractory cutaneous…”
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Clinical and pharmacologic evaluation of two dosing schedules of indotecan (LMP400), a novel indenoisoquinoline, in patients with advanced solid tumors
Published in Cancer chemotherapy and pharmacology (01-07-2016)“…Purpose Indenoisoquinolines are non-camptothecin topoisomerase I (TopI) inhibitors that overcome the limitations of camptothecins: chemical instability and…”
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A pharmacokinetic analysis of cisplatin and 5-fluorouracil in a patient with esophageal cancer on peritoneal dialysis
Published in Cancer chemotherapy and pharmacology (01-02-2016)“…Background Very little is known about the pharmacokinetics of chemotherapeutic agents in patients also being treated with continuous ambulatory peritoneal…”
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LC–MS/MS assay for the quantitation of FdCyd and its metabolites FdUrd and FU in human plasma
Published in Journal of pharmaceutical and biomedical analysis (10-09-2016)“…[Display omitted] •FdCyd is a DNA methylation inhibitor undergoing Phase I and II trials.•An LC–MS/MS assay from 5 to 3000ng/mL in 0.2mL plasma was…”
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A Phase I, Pharmacokinetic and Pharmacodynamic Study on Vorinostat in Combination with 5-Fluorouracil, Leucovorin, and Oxaliplatin in Patients with Refractory Colorectal Cancer
Published in Clinical cancer research (01-05-2009)“…Purpose: We conducted a phase I study to determine the maximum tolerated dose of vorinostat in combination with fixed doses of 5-fluorouracil (FU), leucovorin,…”
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Effect of age on the pharmacokinetics of busulfan in patients undergoing hematopoietic cell transplantation; an alliance study (CALGB 10503, 19808, and 100103)
Published in Cancer chemotherapy and pharmacology (01-11-2014)“…Purpose Older patients with acute myeloid leukemia (AML) and myelodysplastic syndrome have often been excluded from myeloablative-conditioning regimens…”
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Oral and intravenous pharmacokinetics of 5-fluoro-2′-deoxycytidine and THU in cynomolgus monkeys and humans
Published in Cancer chemotherapy and pharmacology (01-10-2015)“…Introduction 5-Fluoro-2′-deoxycytidine (FdCyd; NSC48006), a fluoropyrimidine nucleoside inhibitor of DNA methylation, is degraded by cytidine deaminase (CD)…”
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A liquid chromatography–electrospray ionization tandem mass spectrometric assay for quantitation of the histone deacetylase inhibitor, vorinostat (suberoylanilide hydroxamicacid, SAHA), and its metabolites in human serum
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (18-08-2006)“…Vorinostat (suberoylanilide hydroxamic acid, SAHA) is undergoing evaluation as an antineoplastic agent. We developed a liquid chromatography–tandem mass…”
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Rapid Homogeneous Immunoassay to Quantify Gemcitabine in Plasma for Therapeutic Drug Monitoring
Published in Therapeutic drug monitoring (01-06-2017)“…Gemcitabine (2',2'-difluoro-2'-deoxycytidine) is a nucleoside analog used as a single agent and in combination regimens for the treatment of a variety of solid…”
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