⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for Cetuximab With or Without Brivanib in Treating Patients With K-Ras Wild Type Tumours and Metastatic Colorectal Cancer

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Cetuximab With or Without Brivanib in Treating Patients With K-Ras Wild Type Tumours and Metastatic Colorectal Cancer

Official Title: A Phase III Randomized Study of Brivanib Alaninate (BMS-582664) in Combination With Cetuximab (Erbitux®) Versus Placebo in Combination With Cetuximab (Erbitux®) in Patients With K-RAS Wild Type Tumors Previously Treated With Combination Chemotherapy for Metastatic Colorectal Carcinoma

Study ID: NCT00640471

Study Description

Brief Summary: RATIONALE: Brivanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. It is not yet known whether giving brivanib together with cetuximab is more effective than cetuximab alone in treating patients with metastatic colorectal cancer. PURPOSE: This randomized phase III trial is studying cetuximab to see how well it works compared with cetuximab given together with brivanib in treating patients with metastatic colorectal cancer.

Detailed Description: OBJECTIVES: Primary * To compare the overall survival of patients with previously treated K-Ras wild type metastatic colorectal carcinoma treated with brivanib alaninate in combination with cetuximab versus placebo in combination with cetuximab. Secondary * To compare the progression-free survival of these patients. * To compare the objective response rate and duration of response in these patients. * To compare the quality of life of these patients. * To compare the health utilities of these patients. * To conduct a comparative economic evaluation of these patients. * To evaluate the safety profile of this regimen in these patients. * To explore an association between FGF-2, BRAF mutations, amphiregulin (AREG) and epiregulin (EREG) as determined from paraffin embedded tumor specimens and the potential for clinical benefit from the addition of brivanib alaninate or placebo to cetuximab in terms of overall survival, progression-free survival and objective response rate compared to cetuximab alone. * To explore associations with mRNA and/or protein expression and/or variations in genes associated with epidermal growth factor (EGF), vascular endothelial growth factor (VEGF), angiogenesis, and other related pathways and the potential for clinical benefit from the addition of brivanib alaninate to cetuximab in terms of overall survival, progression-free survival, and objective response rate compared to cetuximab alone. * To explore an association with changes of Collagen IV in the blood and the potential for clinical benefit from the addition of brivanib alaninate to cetuximab in terms of overall survival, progression-free survival and objective response rate compared to cetuximab alone. * To establish a comprehensive tumor bank linked to a clinical database for the further study of molecular markers in colorectal cancer. OUTLINE: This is a multicenter study. Patients are stratified according to participating center and ECOG performance status (0-1 vs 2). Patients are randomized to 1 of 2 arms. * Arm I: Patients receive oral brivanib alaninate once daily and cetuximab IV over 60-120 minutes once weekly. * Arm II: Patients receive oral placebo once daily and cetuximab IV over 60-120 minutes once weekly. In both arms, treatment continues in the absence of disease progression or unacceptable toxicity. Tumor tissue and blood samples are collected for correlative studies. Samples are analyzed for biomarker levels (Collagen IV, FGF-2, and epiregulin, amphiregulin, and BRAF mutation status) and correlation with response. After completion of study treatment, patients are followed at 4 weeks and then every 8 weeks thereafter.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Tom Baker Cancer Centre, Calgary, Alberta, Canada

Cross Cancer Institute, Edmonton, Alberta, Canada

BCCA - Abbotsford Centre, Abbotsford, British Columbia, Canada

BCCA - Cancer Centre for the Southern Interior, Kelowna, British Columbia, Canada

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

BCCA - Vancouver Cancer Centre, Vancouver, British Columbia, Canada

CancerCare Manitoba, Winnipeg, Manitoba, Canada

The Moncton Hospital, Moncton, New Brunswick, Canada

The Vitalite Health Network - Dr. Leon Richard, Moncton, New Brunswick, Canada

Atlantic Health Sciences Corporation, Saint John, New Brunswick, Canada

Dr. H. Bliss Murphy Cancer Centre, St. John's, Newfoundland and Labrador, Canada

The Royal Victoria Hospital, Barrie, Ontario, Canada

Juravinski Cancer Centre at Hamilton Health Sciences, Hamilton, Ontario, Canada

Cancer Centre of Southeastern Ontario at Kingston, Kingston, Ontario, Canada

Grand River Regional Cancer Centre, Kitchener, Ontario, Canada

London Regional Cancer Program, London, Ontario, Canada

Stronach Regional Health Centre at Southlake, Newmarket, Ontario, Canada

Lakeridge Health Oshawa, Oshawa, Ontario, Canada

Ottawa Health Research Institute - General Division, Ottawa, Ontario, Canada

Algoma District Cancer Program, Sault Ste. Marie, Ontario, Canada

Niagara Health System, St. Catharines, Ontario, Canada

Thunder Bay Regional Health Science Centre, Thunder Bay, Ontario, Canada

Toronto East General Hospital, Toronto, Ontario, Canada

Odette Cancer Centre, Toronto, Ontario, Canada

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

Univ. Health Network-Princess Margaret Hospital, Toronto, Ontario, Canada

PEI Cancer Treatment Centre,Queen Elizabeth Hospital, Charlottetown, Prince Edward Island, Canada

Hopital Charles LeMoyne, Greenfield Park, Quebec, Canada

L'Hotel-Dieu de Levis, Levis, Quebec, Canada

CHUM - Hopital Notre-Dame, Montreal, Quebec, Canada

McGill University - Dept. Oncology, Montreal, Quebec, Canada

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

CHUQ-Pavillon Hotel-Dieu de Quebec, Quebec City, Quebec, Canada

CHA-Hopital Du St-Sacrement, Quebec City, Quebec, Canada

Centre hospitalier universitaire de Sherbrooke, Sherbrooke, Quebec, Canada

Allan Blair Cancer Centre, Regina, Saskatchewan, Canada

Saskatoon Cancer Centre, Saskatoon, Saskatchewan, Canada

Contact Details

Name: Lillian L. Siu, MD, FRCPC

Affiliation: Princess Margaret Hospital, Canada

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: