Tirapazamine, Cisplatin, and Radiation Therapy in Treating Patients With Stage IB, Stage II, Stage III, or Stage IVA Cervical Cancer

• Status: Completed
• Trial end date: 2010-01-01
• Target enrollment: 0
• Participant gender: Female

Summary

RATIONALE: Drugs used in chemotherapy, such as tirapazamine and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Tirapazamine may help cisplatin kill more tumor cells by making tumor cells more sensitive to the drug. Radiation therapy uses high-energy x-rays to kill tumor cells. Tirapazamine may also make tumor cells more sensitive to radiation therapy. Giving radiation therapy in different ways together with combination chemotherapy may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of tirapazamine when given together with cisplatin and radiation therapy in treating patients with stage IB, stage II, stage III, or stage IVA cervical cancer.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Peter MacCallum Cancer Centre, Australia
• Collaborator: National Cancer Institute (NCI)
• Treatments: Cisplatin; Tirapazamine

Criteria

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed squamous cell carcinoma, adenocarcinoma, or adenosquamous cell carcinoma of the cervix

• Stage IB, IIA, IIB, III, or IVA disease

• No evidence of involvement of para-aortic nodes by CT scan, MRI, fluorodeoxyglucose positron emission tomography, or lymphadenectomy

• Involvement of common iliac nodes allowed

• No evidence of distant metastases

PATIENT CHARACTERISTICS:

Age

• Any age

Performance status

• ECOG 0-2

Life expectancy

• More than 6 months

Hematopoietic

• Absolute neutrophil count ≥ 1,500/mm^3

• Platelet count ≥ 100,000/mm^3

Hepatic

• Bilirubin < 1.25 times upper limit of normal (ULN)

• AST and ALT ≤ 3 times ULN

Renal

• Calculated creatinine clearance ≥ 60 mL/min OR

• Glomerular filtration rate ≥ 60 mL/min

Cardiovascular

• No significant cardiac disease that would preclude IV fluid load required for administration of cisplatin

• No symptomatic congestive heart failure

• No unstable angina pectoris

• No cardiac arrhythmia

Other

• No symptomatic peripheral neuropathy ≥ grade 2

• No clinically significant sensori-neural hearing impairment interfering with activities of daily living or requiring a hearing aid

• Audiometric changes alone of any severity allowed

• No history of allergic reaction attributed to compounds of similar chemical or biological composition to tirapazamine or cisplatin

• No other invasive malignancy within the past 5 years except nonmelanoma skin cancer

• No ongoing or active infection

• No psychiatric illness or social situation that would preclude study compliance

• No other concurrent uncontrolled illness

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy

• No concurrent epoetin alfa

• No concurrent prophylactic filgrastim (G-CSF) or sargramostim (GM-CSF)

• No concurrent pegfilgrastim

Chemotherapy

• No prior chemotherapy for another malignancy

Endocrine therapy

• Not specified

Radiotherapy

• No prior pelvic or abdominal radiotherapy for another malignancy

• No prior radiotherapy to ≥ 15% of bone marrow-bearing areas

• No concurrent intensity-modulated radiotherapy

• No concurrent interstitial brachytherapy

Surgery

• Not specified

Other

• No prior treatment for invasive cervical cancer

• No other concurrent therapeutic investigational agents

• No other concurrent anticancer therapy

• No concurrent systemic retinoids

• No concurrent amifostine

• No concurrent combination antiretroviral therapy for HIV-positive patients