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A phase II trial of pyrazoloacridine (PZA) in squamous cell carcinoma of the cervix: A gynecologic oncology group study

  • Steven C. Plaxe
  • , John A. Blessing
  • , George Olt
  • , Nader Husseinzadah
  • , Samuel S. Lentz
  • , Koen DeGeest
  • , Fidel A. Valea

Research output: Contribution to journalArticlepeer-review

Abstract

Purpose: The Gynecologic Oncology Group performed a phase II study to determine the response rate to pyrazoloacridine (PZA) in patients with advanced, persistent or recurrent squamous carcinoma of the cervix. Methods: PZA was administered intravenously over 3 h every 3 weeks. A dose of 760 mg/m2 was given to the first 11 patients and was reduced to 560 mg/m2 for subsequent patients. The dose reduction was undertaken because of unexpected severe neutropenia among the initial patients. Results: Among 24 evaluable patients, 21 of whom had prior chemotherapy, there was one, brief, complete response (4.2%) and no partial responses. The major toxicity was neutropenia. Conclusion: PZA at the dose and schedule employed, has insignificant activity in this population.

Original languageEnglish (US)
Pages (from-to)151-154
Number of pages4
JournalCancer Chemotherapy and Pharmacology
Volume50
Issue number2
DOIs
StatePublished - 2002
Externally publishedYes

Funding

Acknowledgements This study was supported by National Cancer Institute grants of the Gynecologic Oncology Group Administrative Office (CA 27469) and the Gynecologic Oncology Group Statistical Office (CA 37517).

FundersFunder number
Gynecologic Oncology Group Administrative OfficeCA 27469
Gynecologic Oncology Group Statistical Office
National Institute of Health-National Cancer InstituteU10CA037517

    Keywords

    • Cervical cancer
    • PZA
    • Pyrazoloacridine

    ASJC Scopus subject areas

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

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