An update of a phase II study of paclitaxel in advanced or recurrent squamous cell cancer of the cervix

Andrzej P. Kudelka, Rodger Winn, Creighton L. Edwards, G. Downey, Harvey Greenberg, S. R. Dakhil, Ralph S. Freedman, Salvatore LoCoco, J. Umbreit, James E. Delmore, Susan Arbuck, Evelyne Loyer, Patsy Gacrama, Rebecca Fueger, John J. Kavanagh

    Research output: Contribution to journalArticlepeer-review

    56 Scopus citations

    Abstract

    Thirty-two evaluable patients with squamous cell cancer of the cervix were treated with i.v. paclitaxel 250 mg/m2 over 3 h every 21 days. They received standard premedications and granulocyte colony stimulating factor (G-CSF) support (5 μg/kg/day). Median (range) age was 49 (29-81) years and performance status Zubrod was 1 (0-2). One patient had a complete response and seven patients had a partial response (25%, 95% CI 8-38%). The median survival was 7.3 months. Granulocytopenia was brief and non-cumulative. G-CSF was used for a median (range) of 8 (1-15) days per cycle. In conclusion: paclitaxel is active in patients with squamous cell cancer of the cervix and is well tolerated in this dose schedule with G-CSF support.

    Original languageEnglish (US)
    Pages (from-to)657-661
    Number of pages5
    JournalAnti-cancer drugs
    Volume8
    Issue number7
    DOIs
    StatePublished - 1997

    Keywords

    • Cervix cancer
    • Granulocyte colony stimulating factor
    • Paclitaxel

    ASJC Scopus subject areas

    • Oncology
    • Pharmacology
    • Pharmacology (medical)
    • Cancer Research

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