Sc. Plaxe et al., A phase II trial of pyrazoloacridine (PZA) in squamous carcinoma of the cervix - A Gynecologic Oncology Group study, INV NEW DR, 19(1), 2001, pp. 77-80
Purpose: The Gynecologic Oncology Group performed a Phase II study to deter
mine the response rate of Pyrazoloacridine (PZA) in patients with advanced,
persistent or recurrent squamous carcinoma of the cervix. Methods: PZA was
administered at a dose of 750 mg/m(2) intravenously over three hours every
three weeks. Results: Among 21 evaluable patients, there were no complete
and one (4.2%) partial response. The major toxicities were hematologic. Con
clusion: PZA at the dose and schedule employed has insignificant activity i
n this population.