Flavopiridol in Treating Patients With Metastatic Malignant Melanoma
Melanoma (Skin)

About this trial
This is an interventional treatment trial for Melanoma (Skin) focused on measuring stage IV melanoma
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed metastatic malignant melanoma not amenable to standard curative therapies No prior regional or systemic therapy for metastatic disease Measurable disease At least 20 mm by conventional techniques OR At least 10 mm by spiral CT scan Bone lesions not considered measurable No known CNS metastases PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: At least 12 weeks Hematopoietic: Absolute granulocyte count at least 1,500/mm3 Platelet count at least 100,000/mm3 Hepatic: Bilirubin no greater than upper limit of normal (ULN) AST no greater than 2.5 times ULN Renal: Creatinine no greater than ULN Cardiovascular: If history of cardiac disease, ejection fraction greater than 50% No clinically significant cardiac symptomology Pulmonary: If history of pulmonary disease, FEV1, FVC, and TLC greater than 60% predicted and DLCO greater than 50% predicted No clinically significant pulmonary symptomology Other: Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception No other concurrent serious disease PRIOR CONCURRENT THERAPY: Biologic therapy: At least 4 weeks since prior adjuvant immunotherapy allowed No prior immunotherapy for metastatic disease Chemotherapy: No prior chemotherapy for metastatic disease No other concurrent chemotherapy Endocrine therapy: At least 4 weeks since prior adjuvant hormonal therapy Radiotherapy: At least 4 weeks since prior radiotherapy and recovered Must have measurable disease outside irradiated area OR Evidence of progression or new lesions in irradiated area No more than 25% of functioning bone marrow irradiated No concurrent radiotherapy to sole site of measurable disease Surgery: At least 4 weeks since prior major surgery Other: No other concurrent anticancer therapy or investigational anticancer agents
Sites / Locations
- Tom Baker Cancer Center - Calgary
- Lethbridge Cancer Clinic
- Penticton Regional Hospital
- Prostate Centre at Vancouver General Hospital
- St. Paul's Hospital - Vancouver
- G. Steinhoff Clinical Research
- Moncton Hospital
- Doctor Leon Richard Oncology Centre
- Saint John Regional Hospital
- Newfoundland Cancer Treatment and Research Foundation
- Nova Scotia Cancer Centre
- Royal Victoria Hospital, Barrie
- William Osler Health Centre
- Hamilton and Disrict Urology Association
- London Health Sciences Centre
- Trillium Health Centre
- Credit Valley Hospital
- York County Hospital
- North York General Hospital, Ontario
- Male Health Centre/CMX Research Inc.
- Lakeridge Health Oshawa
- Ottawa Regional Cancer Centre
- Peterborough Oncology Clinic
- Scarborough Hospital - General Site
- Hotel Dieu Health Sciences Hospital - Niagara
- Northeastern Ontario Regional Cancer Centre, Sudbury
- Northwestern Ontario Regional Cancer Centre, Thunder Bay
- Toronto East General Hospital
- Toronto Sunnybrook Regional Cancer Centre
- St. Michael's Hospital - Toronto
- Mount Sinai Hospital - Toronto
- Toronto General Hospital
- Princess Margaret Hospital
- Women's College Campus, Sunnybrook and Women's College Health Science Center
- Saint Joseph's Health Centre - Toronto
- Humber River Regional Hospital
- Cancer Care Ontario - Windsor Regional Cancer Centre
- Queen Elizabeth Hospital, PEI
- CHUS-Hopital Fleurimont
- Centre Hospitalier Regional de Lanaudiere
- Maisonneuve-Rosemont Hospital
- McGill University
- Centre Hospitalier de l'Universite' de Montreal
- Hotel Dieu de Montreal
- Hopital Du Sacre-Coeur de Montreal
- Centre Hospitalier Universitaire de Quebec
- Hopital du Saint-Sacrament, Quebec
- L'Hopital Laval
- Allan Blair Cancer Centre
- Saskatoon Cancer Centre