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    Underreporting of Gastrointestinal Stromal Tumors: Is the True Incidence Being Captured?

    Hospital cancer registries are only required to report gastrointestinal stromal tumors (GISTs) if labeled malignant or metastatic, leading to potential loss of cases in national cancer registries. Our objectiv...

    Audrey H. Choi, John B. Hamner, Shaila J. Merchant in Journal of Gastrointestinal Surgery (2015)

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    First-in-human phase 1/2a trial of CRLX101, a cyclodextrin-containing polymer-camptothecin nanopharmaceutical in patients with advanced solid tumor malignancies

    Patients with advanced solid malignancies were enrolled to an open-label, single-arm, dose-escalation study, in which CRLX101 was administered intravenously over 60 min among two dosing schedules, initially we...

    Glen J. Weiss, Joseph Chao, Jeffrey D. Neidhart in Investigational New Drugs (2013)

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    Phase II trial of bryostatin-1 in combination with cisplatin in patients with recurrent or persistent epithelial ovarian cancer: a California cancer consortium study

    Background The California Cancer Consortium has performed a Phase II trial of infusional bryostatin, a protein kinase C inhibitor isolated from the marine invertebrate bryozoan, Bugula Neritina, ...

    Robert J. Morgan Jr, Lucille Leong, Warren Chow, David Gandara in Investigational New Drugs (2012)

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    Plasma and cerebrospinal fluid pharmacokinetics of topotecan in a phase I trial of topotecan, tamoxifen, and carboplatin, in the treatment of recurrent or refractory brain or spinal cord tumors

    This study was designed to ascertain the dose-limiting toxicities (DLT) and maximally tolerated doses of the combination of fixed-dose tamoxifen and carboplatin, with escalating doses of topotecan, and to dete...

    Robert J. Morgan, Timothy Synold, Adam Mamelak in Cancer Chemotherapy and Pharmacology (2010)

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    A phase I study of oxaliplatin in combination with gemcitabine: correlation of clinical outcome with gene expression

    Oxaliplatin has in vitro activity similar to or higher than other platinum agents. Preclinically, gemcitabine has demonstrated synergy when combined with platinum compounds. These facts formed the rationale fo...

    Stephen Shibata, Warren Chow, Paul Frankel in Cancer Chemotherapy and Pharmacology (2007)

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    Phase II trial of carboplatin and infusional cyclosporine in platinum-resistant recurrent ovarian cancer

    To determine the response rate to 26-h continuous infusion cyclosporine A (CSA) combined with a fixed dose level of carboplatin (CBDCA) in patients with recurrent ovarian cancer, and to determine the effect of...

    Robert J. Morgan Jr., Timothy W. Synold in Cancer Chemotherapy and Pharmacology (2004)

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    Phase I study of cisdiamminedichloroplatinum in combination with azidothymidine in the treatment of patients with advanced malignancies

    Azidothymidine (AZT, zidovudine) has been shown to reverse cisplatin resistance in cell culture. This phase I study was performed to determine the maximally tolerated dose (MTD) and dose-limiting toxicities of...

    Robert J. Morgan Jr, Edward M. Newman in Cancer Chemotherapy and Pharmacology (2003)

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    Phase I pharmacodynamic study of time and sequence dependency of hydroxyurea in combination with gemcitabine: a California Cancer Consortium Trial

    Preclinical studies in our laboratory have demonstrated that prior exposure to hydroxyurea increases the percentage of cells in S phase, enhancing the cytotoxicity of subsequent gemcitabine treatment in human...

    Yun Yen, Warren Chow, Lucille Leong, Kim Margolin in Cancer Chemotherapy and Pharmacology (2002)

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    Continuous infusion prochlorperazine: pharmacokinetics, antiemetic efficacy, and feasibility of high-dose therapy

    Purpose: The purpose of these sequential phase I studies was to evaluate the antiemetic efficacy and pharmacokinetics of high-dose continuous infusion prochlorperazine. Methods: A total of 52 pat...

    Robert J. Morgan Jr, Timothy Synold, Brian I. Carr in Cancer Chemotherapy and Pharmacology (2001)

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    A phase I study of carboplatin and etoposide administered in conjunction with dipyridamole, prochlorperazine and cyclosporine A

    Purpose: In recognition of the variety of available chemotherapeutic modulating agents and their potential to enhance the efficacy of platinum-based therapy, we embarked upon a phase I study to investigate the f...

    James W. Raschko, Timothy W. Synold, Warren Chow in Cancer Chemotherapy and Pharmacology (2000)

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    Pharmacokinetics and toxicity of 120-hour continuous-infusion hydroxyurea in patients with advanced solid tumors

     A group of 18 patients with advanced cancer were entered on a phase I study of a 120-h continuous intravenous infusion of hydroxyurea. The dose of hydroxyurea was escalated in cohorts of patients from 1 to 2 ...

    E. M. Newman, Mary Carroll, Steven A. Akman in Cancer Chemotherapy and Pharmacology (1996)

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    Mitomycin C and menadione for the treatment of lung cancer: a phase II trial

    A phase II trial of menadione [2.5 gm/m2 as a continuous intravenous (iv) infusion over 48 hours] followed by mitomycin C (10–20 mg/m2 iv bolus) administered every 4 to 6 weeks was performed in 23 patients with a...

    Merry Tetef, Kim Margolin, Chul Ahn, Steven Akman, Warren Chow in Investigational New Drugs (1995)

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    Mitomycin C and menadione for the treatment of advanced gastrointestinal cancers: a phase II trial

    A phase II trial of menadione (2.5 g/m2 as a continuous intravenous infusion over 48 h) followed by mitomycin C (10–20 mg/m2 i.v. bolus) administered every 4–6 weeks was performed in 43 patients with advanced gas...

    Merry Tetef, Kim Margolin, Chul Ahn in Journal of Cancer Research and Clinical On… (1995)