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    Article

    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 I trial of menadiol diphosphate (vitamin K3) in advanced malignancy

    Based on the activity of menadione (M) in the human tumor stem cell assay, we conducted a phase I trial of M in patients with advanced cancer. Forty patients (19 men, 21 women) were treated with 90 courses of ...

    Dean Lim MD, Robert J. Morgan Jr., Steven Akman, Kim Margolin in Investigational New Drugs (2005)

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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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    A phase I trial of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone in combination with gemcitabine for patients with advanced cancer

    3-Aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP), a new and potent inhibitor of ribonucleotide reductase (RR), increases the cellular uptake, DNA incorporation, and cytotoxicity of gemcitabine in tumo...

    Yun Yen, Kim Margolin, James Doroshow in Cancer Chemotherapy and Pharmacology (2004)

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    Feasibility and pharmacokinetic study of infusional dexrazoxane and dose-intensive doxorubicin administered concurrently over 96 h for the treatment of advanced malignancies

    Dexrazoxane administration prior to short infusion doxorubicin prevents anthracycline-related heart damage. Since delivery of doxorubicin by 96-h continuous intravenous infusion also reduces cardiac injury, we...

    Warren A. Chow, Timothy W. Synold, Merry L. Tetef 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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    Dolastatin-10 in Metastatic Melanoma: A Phase II and Pharmokinetic Trial of the California Cancer Consortium

    Dolastatin-10 is a novel pentapeptide agentoriginally isolated from the marine molluskDolabella auricularia with amechanism of antitumor activity thatinvolves the inhibition of microtubuleassembly. We performed a...

    Kim Margolin, Jeffrey Longmate, Timothy W. Synold in Investigational New Drugs (2001)

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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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    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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    Fluorouracil and Leucovorin in Advanced Breast Cancer

    It is clear from the studies summarized above that the combination of leucovorin and 5-FU can salvage 15–20% of heavily-pretreated patients with advanced breast cancer. In previously-untreated patients, the co...

    James H. Doroshow, Kim Margolin in Novel Approaches to Selective Treatments o… (1993)

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    Phase II study of 4 ′ -deoxydoxorubicin (esorubicin) in advanced or metastatic adenocarcinoma of the stomach

    4 ′-deoxydoxorubicin (DxDx) was administered to 17 patients with locally advanced or metastatic gastric adenocarcinoma. Treatment cycles were repeated every 21 days. 15 eligible patients with a Karnofsky perfo...

    George Somlo, James Doroshow, Steven Akman, Lucille Leong in Investigational New Drugs (1991)

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    3-Deazaguanine: Report of a phase I trial and drug-related cardiac toxicity

    3-Deazaguanine (Dezaguanine), a purine antimetabolite, was evaluated in a phase I trial in 42 patients with advanced solid tumors. Dezaguanine was given as a weekly intravenous infusion for three consecutive w...

    Kim Margolin, James Doroshow, Lucille Leong, Steven Akman in Investigational New Drugs (1990)