Overview
Irinotecan and Cisplatin in Treating Patients With Locally Advanced or Metastatic Penile Cancer
Status:
Completed
Completed
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
Male
Male
Summary
RATIONALE: Drugs used in chemotherapy such as irinotecan and cisplatin use different ways to stop tumor cells from dividing so they stop growing or die. Combining irinotecan with cisplatin may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining irinotecan with cisplatin in treating patients who have locally advanced or metastatic penile cancer.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
European Organisation for Research and Treatment of Cancer - EORTCTreatments:
Camptothecin
Cisplatin
Irinotecan
Criteria
DISEASE CHARACTERISTICS:- Histologically confirmed penile squamous cell carcinoma
- Locally advanced or metastatic disease
- T3, N1-2 OR T4, N3, M1
- Measurable disease outside of any previously irradiated field
- No clinical signs of brain metastases
PATIENT CHARACTERISTICS:
Age
- 75 and under
Performance status
- WHO 0-2
Life expectancy
- Not specified
Hematopoietic
- Absolute neutrophil count at least 2,000/mm^3
- Platelet count at least 100,000/mm^3
Hepatic
- Bilirubin no greater than 1.5 times upper limit of normal (ULN)
- Alkaline phosphatase no greater than 2.5 times ULN (5 times ULN in the presence of
liver metastases)
- Transaminases no greater than 2.5 times ULN (5 times ULN in the presence of liver
metastases)
Renal
- Glomerular filtration rate at least 60 mL/min
Gastrointestinal
- No chronic diarrhea
- No unresolved bowel obstruction
- No chronic inflammatory bowel disease (e.g., Crohn's disease or ulcerative colitis)
Other
- No other prior or concurrent malignancy except adequately treated skin cancer
- No psychological, familial, sociological, or geographical condition that would
preclude study compliance and follow-up
PRIOR CONCURRENT THERAPY:
Biologic therapy
- Not specified
Chemotherapy
- No prior chemotherapy
Endocrine therapy
- Not specified
Radiotherapy
- See Disease Characteristics
- More than 4 weeks since prior radiotherapy
- No concurrent radiotherapy for pain control
Surgery
- Not specified
Other
- No other concurrent experimental or anticancer therapy