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Spots Global Cancer Trial Database for Thalidomide and Prednisone Following Peripheral Stem Cell Transplantation in Treating Patients With Multiple Myeloma

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Trial Identification

Brief Title: Thalidomide and Prednisone Following Peripheral Stem Cell Transplantation in Treating Patients With Multiple Myeloma

Official Title: A Randomized Phase II Dose Finding Study Of Thalidomide And Prednisone As Maintenance Therapy Following Autologous Stem Cell Transplant In Patients With Multiple Myeloma

Study ID: NCT00006890

Study Description

Brief Summary: RATIONALE: Thalidomide may stop the growth of multiple myeloma by stopping blood flow to the tumor. Prednisone may be effective in preventing relapse of multiple myeloma. PURPOSE: Randomized phase II trial to compare the effectiveness of two doses of thalidomide combined with prednisone following peripheral stem cell transplantation in treating patients who have multiple myeloma.

Detailed Description: OBJECTIVES: I. Determine which dose of thalidomide (200 mg vs 400 mg) combined with prednisone is the optimally tolerated dose when used as maintenance therapy following autologous stem cell transplantation in patients with multiple myeloma. II. Compare the response rate in patients treated with these regimens. III. Compare the progression-free and overall survival in patients treated with these regimens. OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to age (60 and over vs under 60). Within 60-100 days after autologous stem cell transplantation, patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive lower dose oral thalidomide daily and oral prednisone every other day. Arm II: Patients receive higher dose thalidomide daily and oral prednisone every other day. Treatment continues for 2 years in the absence of disease progression or unacceptable toxicity. Patients are followed monthly for 6 months, every 3 months, and then at time of disease progression. PROJECTED ACCRUAL: A total of 40-80 patients (20-40 per arm) will be accrued for this study within 17-21 months.

Eligibility

Minimum Age: 16 Years

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

St. Mary's/Duluth Clinic Health System, Duluth, Minnesota, United States

Tom Baker Cancer Center - Calgary, Calgary, Alberta, Canada

Lethbridge Cancer Clinic, Lethbridge, Alberta, Canada

Burnaby Hospital Regional Cancer Centre, Burnaby, British Columbia, Canada

Nanaimo Cancer Clinic, Nanaimo, British Columbia, Canada

Penticton Regional Hospital, Penticton, British Columbia, Canada

British Columbia Cancer Agency - Fraser Valley Cancer Centre, Surrey, British Columbia, Canada

Prostate Centre at Vancouver General Hospital, Vancouver, British Columbia, Canada

British Columbia Cancer Agency, Vancouver, British Columbia, Canada

St. Paul's Hospital - Vancouver, Vancouver, British Columbia, Canada

G. Steinhoff Clinical Research, Victoria, British Columbia, Canada

Moncton Hospital, Moncton, New Brunswick, Canada

Doctor Leon Richard Oncology Centre, Moncton, New Brunswick, Canada

Saint John Regional Hospital, Saint John, New Brunswick, Canada

Newfoundland Cancer Treatment and Research Foundation, St. Johns, Newfoundland and Labrador, Canada

Nova Scotia Cancer Centre, Halifax, Nova Scotia, Canada

Cape Breton Cancer Centre, Sydney, Nova Scotia, Canada

Royal Victoria Hospital, Barrie, Barrie, Ontario, Canada

William Osler Health Centre, Brampton, Ontario, Canada

Hamilton and Disrict Urology Association, Hamilton, Ontario, Canada

London Health Sciences Centre, London, Ontario, Canada

Cancer Care Ontario-London Regional Cancer Centre, London, Ontario, Canada

Markham Stouffville Hospital, Markham, Ontario, Canada

Trillium Health Centre, Mississauga, Ontario, Canada

Credit Valley Hospital, Mississauga, Ontario, Canada

York County Hospital, Newmarket, Ontario, Canada

North York General Hospital, Ontario, North York, Ontario, Canada

Male Health Centre/CMX Research Inc., Oakville, Ontario, Canada

Lakeridge Health Oshawa, Oshawa, Ontario, Canada

Ottawa Regional Cancer Centre - General Campus, Ottawa, Ontario, Canada

Ottawa Regional Cancer Center - General Division, Ottawa, Ontario, Canada

Peterborough Oncology Clinic, Peterborough, Ontario, Canada

Scarborough Hospital - General Site, Scarborough, Ontario, Canada

Hotel Dieu Health Sciences Hospital - Niagara, St. Catharines, Ontario, Canada

Northeastern Ontario Regional Cancer Centre, Sudbury, Sudbury, Ontario, Canada

Northwestern Ontario Regional Cancer Centre, Thunder Bay, Thunder Bay, Ontario, Canada

Toronto East General Hospital, Toronto, Ontario, Canada

Toronto Sunnybrook Regional Cancer Centre, Toronto, Ontario, Canada

St. Michael's Hospital - Toronto, Toronto, Ontario, Canada

Mount Sinai Hospital - Toronto, Toronto, Ontario, Canada

Toronto General Hospital, Toronto, Ontario, Canada

Princess Margaret Hospital, Toronto, Ontario, Canada

Women's College Campus, Sunnybrook and Women's College Health Science Center, Toronto, Ontario, Canada

Saint Joseph's Health Centre - Toronto, Toronto, Ontario, Canada

Humber River Regional Hospital, Weston, Ontario, Canada

Cancer Care Ontario - Windsor Regional Cancer Centre, Windsor, Ontario, Canada

Queen Elizabeth Hospital, PEI, Charlottetown, Prince Edward Island, Canada

CHUS-Hopital Fleurimont, Fleurimont, Quebec, Canada

Hopital Charles Lemoyne, Greenfield Park, Quebec, Canada

Centre Hospitalier Regional de Lanaudiere, Joliette, Quebec, Canada

Maisonneuve-Rosemont Hospital, Montreal, Quebec, Canada

McGill University, Montreal, Quebec, Canada

Centre Hospitalier de l'Universite' de Montreal, Montreal, Quebec, Canada

Hotel Dieu de Montreal, Montreal, Quebec, Canada

Hopital Sainte Justine, Montreal, Quebec, Canada

Hopital Du Sacre-Coeur de Montreal, Montreal, Quebec, Canada

Kells Medical Research Group Inc., Pointe Claire, Quebec, Canada

CHU de Quebec - L'Hotel-Dieu de Quebec, Quebec City, Quebec, Canada

Hopital du Saint-Sacrament, Quebec, Quebec City, Quebec, Canada

Centre Hospitalier Regional de Rimouski, Rimouski, Quebec, Canada

L'Hopital Laval, Ste-Foy, Quebec, Canada

Allan Blair Cancer Centre, Regina, Saskatchewan, Canada

Saskatoon Cancer Centre, Saskatoon, Saskatchewan, Canada

Lions Gate Hospital, North Vancouver, , Canada

Contact Details

Name: A. Keith Stewart, MD

Affiliation: Princess Margaret Hospital, Canada

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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