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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.
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Plaxe, S.C., Blessing, J.A., Olt, G. et al. A phase II trial of pyrazoloacridine (PZA) in squamous cell carcinoma of the cervix: a Gynecologic Oncology Group study. Cancer Chemother Pharmacol 50, 151–154 (2002). https://doi.org/10.1007/s00280-002-0470-2
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DOI: https://doi.org/10.1007/s00280-002-0470-2