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/m(2) was given to the first 11 patients and was reduced to 560 mg/m(2) 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.
Publication types
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Clinical Trial
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Clinical Trial, Phase II
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Multicenter Study
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Acridines / administration & dosage
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Acridines / adverse effects
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Acridines / therapeutic use*
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Adult
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Aged
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Carcinoma, Squamous Cell / drug therapy*
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Carcinoma, Squamous Cell / pathology
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Drug Administration Schedule
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Enzyme Inhibitors / administration & dosage
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Enzyme Inhibitors / adverse effects
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Enzyme Inhibitors / therapeutic use
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Female
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Humans
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Infusions, Intravenous
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Intercalating Agents / administration & dosage
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Intercalating Agents / adverse effects
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Intercalating Agents / therapeutic use
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Middle Aged
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Neutropenia / chemically induced
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Nucleic Acid Synthesis Inhibitors / administration & dosage
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Nucleic Acid Synthesis Inhibitors / adverse effects
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Nucleic Acid Synthesis Inhibitors / therapeutic use
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Pyrazoles / administration & dosage
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Pyrazoles / adverse effects
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Pyrazoles / therapeutic use*
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Remission Induction
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Salvage Therapy
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Treatment Outcome
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Uterine Cervical Neoplasms / drug therapy*
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Uterine Cervical Neoplasms / pathology
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Vomiting / chemically induced
Substances
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Acridines
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Enzyme Inhibitors
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Intercalating Agents
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Nucleic Acid Synthesis Inhibitors
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Pyrazoles
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NSC 366140