vintriptol and Leukopenia

vintriptol has been researched along with Leukopenia* in 2 studies

Trials

1 trial(s) available for vintriptol and Leukopenia

ArticleYear
Phase I study of vintriptol, a tryptophan ester of vinblastine.
    European journal of cancer (Oxford, England : 1990), 1991, Volume: 27, Issue:10

    Vintriptol, a tryptophan ester of vinblastine, is a new vinca alkaloid derivative. Preclinical studies have demonstrated its antitumour activity in a large variety of animal models. In this phase I study, 47 patients with advanced cancer were exposed to escalating doses of vintriptol, starting at 6 mg/m2 and following a modified Fibonacci schedule. The drug was administered as an intravenous push on a weekly schedule. Myelosuppression was the dose-limiting toxicity and the maximum tolerated dose was 45 mg/m2. Other toxicities consisted of mild nausea and vomiting and the occurrence of fever and dryness of the mouth immediately after drug administration. Neurotoxicity, a major side-effect of other vinca alkaloids, was insignificant. 1 partial remission in a patient suffering from colorectal cancer and 1 minor response in a patient with a metastatic tumour of the cutaneous appendagous glands were documented. Pharmacokinetics of vintriptol were evaluated at the highest dose levels. A dose schedule of 40 mg/m2 vintriptol per week is recommended for phase II studies.

    Topics: Adult; Aged; Antineoplastic Agents; Drug Evaluation; Female; Fever; Humans; Leukopenia; Male; Middle Aged; Neoplasms; Thrombocytopenia; Vinblastine

1991

Other Studies

1 other study(ies) available for vintriptol and Leukopenia

ArticleYear
A phase I study of vinblastine tryptophan ester.
    Cancer chemotherapy and pharmacology, 1986, Volume: 18, Issue:1

    Vinblastine tryptophan ester (VTrpE) is a new vinca alkaloid derivative that achieves antitumor activity in a large variety of animal models. In this phase I study the drug was given as an i.v. injection over 5 min, once a week or once every 2 weeks. Twenty patients with advanced cancer were entered in this trial. The doses ranged from 2.5 mg/m2 to 35 mg/m2. Myelosuppression is the dose-limiting toxicity, with the risk of leukopenia being more serious than that of thrombocytopenia, but the myelosuppression is always reversible. Neurotoxicity, well documented when other vinca alkaloid derivatives are used, is insignificant. Two cases of disease stabilization have been observed in patients with non-small cell lung cancer. For VTrpE, a dose schedule of 30 mg/m2 per week may be recommended for phase II studies in non-small cell lung cancer.

    Topics: Adult; Child; Drug Evaluation; Female; Humans; Leukopenia; Male; Neoplasms; Thrombocytopenia; Vinblastine

1986