Preliminary report of the activity of docetaxel in advanced or recurrent squamous cell cancer of the cervix

A. P. Kudelka*, C. F. Verschraegen, T. Levy, C. L. Edwards, A. Fishman, R. S. Freedman, A. Kaplan, D. G. Kieback, R. Mante, K. Ende, M. Steger, J. J. Kavanagh

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Eighteen patients with squamous cell cancer of the cervix were treated with i.v. docetaxel 100 mg/m2 over 1 h every 21 days. No patient received prior chemotherapy, except as a radiation sensitizer. Median age was 42 years (range 30-58) and Zubrod performance states was 1 (0-2). Ten (59%) patients had prior surgery and 11 (65%) had prior radiation therapy. Sixteen patients were evaluable for response. Two patients had a partial response (13%; 95% CI 0-32%) and eight (50%; 95% CI 23-77%) had stable disease. Dose reduction to 75 mg/m2 was required in 10 patients and to 55 mg/m2 in one patient. Granulocytopenia was the major hematopoietic toxicity (31% grade 3 and 44% grade 4). Docetaxel is active in patients with squamous cell cancer of the cervix and may be tolerable at this dose schedule.

Original languageEnglish
Pages (from-to)398-401
Number of pages4
JournalAnti-Cancer Drugs
Volume7
Issue number4
DOIs
StatePublished - 1996
Externally publishedYes

Keywords

  • Cervix cancer
  • Docetaxel
  • Granulocyte colony stimulating factor

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