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Spots Global Cancer Trial Database for Sorafenib in Treating Patients at Risk of Relapse After Undergoing Surgery to Remove Kidney Cancer

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Trial Identification

Brief Title: Sorafenib in Treating Patients at Risk of Relapse After Undergoing Surgery to Remove Kidney Cancer

Official Title: SORCE: A Phase III Randomised Double-Blind Study Comparing Sorafenib With Placebo in Patients With Resected Primary Renal Cell Carcinoma at High or Intermediate Risk of Relapse

Study ID: NCT00492258

Conditions

Kidney Cancer

Study Description

Brief Summary: RATIONALE: Sorafenib 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. Giving sorafenib after surgery may kill any tumor cells that remain after surgery. It is not yet known whether sorafenib is more effective than a placebo in treating kidney cancer. PURPOSE: This randomized phase III trial is studying sorafenib to see how well it works compared with a placebo in treating patients at risk of relapse after undergoing surgery to remove kidney cancer.

Detailed Description: OBJECTIVES: * Compare disease-free survival of patients with resected primary renal cell carcinoma at high- or intermediate-risk of relapse treated with a placebo for 3 years vs a placebo for 2 years and sorafenib tosylate for 1 year vs sorafenib tosylate for 3 years. OUTLINE: This is a randomized, placebo-controlled, double-blind, open-label, multicenter study. Patients are randomized to 1 of 3 treatment arms. * Arm I: Patients receive oral placebo twice daily for 3 years in the absence of disease progression or unacceptable toxicity. * Arm II: Patients receive oral sorafenib tosylate twice daily for 1 year and oral placebo twice daily for 2 years in the absence of disease progression or unacceptable toxicity. * Arm III: Patients receive oral sorafenib tosylate twice daily for 3 years in the absence of disease progression or unacceptable toxicity. Patients in arms I and II with progressive disease may cross over and receive treatment in arm III. After completion of study treatment, patients are followed periodically.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Royal Bournemouth Hospital, Bournemouth, England, United Kingdom

Bristol Haematology and Oncology Centre, Bristol, England, United Kingdom

Queen's Hospital, Burton-upon-Trent, England, United Kingdom

Addenbrooke's Hospital, Cambridge, England, United Kingdom

Gloucestershire Oncology Centre at Cheltenham General Hospital, Cheltenham, England, United Kingdom

Derbyshire Royal Infirmary, Derby, England, United Kingdom

Dorset County Hospital, Dorchester, England, United Kingdom

Gloucestershire Royal Hospital, Gloucester, England, United Kingdom

Diana Princess of Wales Hospital, Grimsby, England, United Kingdom

Princess Royal Hospital at Hull and East Yorkshire NHS Trust, Hull, England, United Kingdom

Ipswich Hospital, Ipswich, England, United Kingdom

Leeds Cancer Centre at St. James's University Hospital, Leeds, England, United Kingdom

Leicester Royal Infirmary, Leicester, England, United Kingdom

Lincoln County Hospital, Lincoln, England, United Kingdom

Saint Bartholomew's Hospital, London, England, United Kingdom

Medical Research Council Clinical Trials Unit, London, England, United Kingdom

Guy's Hospital, London, England, United Kingdom

Royal Marsden - London, London, England, United Kingdom

Charing Cross Hospital, London, England, United Kingdom

Maidstone Hospital, Maidstone, England, United Kingdom

Christie Hospital, Manchester, England, United Kingdom

Clatterbridge Centre for Oncology, Merseyside, England, United Kingdom

James Cook University Hospital, Middlesbrough, England, United Kingdom

Northern Centre for Cancer Treatment at Newcastle General Hospital, Newcastle-Upon-Tyne, England, United Kingdom

Mount Vernon Cancer Centre at Mount Vernon Hospital, Northwood, England, United Kingdom

Derriford Hospital, Plymouth, England, United Kingdom

Dorset Cancer Centre, Poole Dorset, England, United Kingdom

Portsmouth Oncology Centre at Saint Mary's Hospital, Portsmouth Hants, England, United Kingdom

Whiston Hospital, Prescot Merseyside, England, United Kingdom

Berkshire Cancer Centre at Royal Berkshire Hospital, Reading, England, United Kingdom

Scarborough General Hospital, Scarborough, England, United Kingdom

Scunthorpe General Hospital, Scunthorpe, England, United Kingdom

Cancer Research Centre at Weston Park Hospital, Sheffield, England, United Kingdom

Wexham Park Hospital, Slough, Berkshire, England, United Kingdom

Southampton General Hospital, Southampton, England, United Kingdom

University Hospital of North Staffordshire, Stoke-On-Trent, England, United Kingdom

Torbay Hospital, Torquay, England, United Kingdom

Aberdeen Royal Infirmary, Aberdeen, Scotland, United Kingdom

Velindre Cancer Center at Velindre Hospital, Cardiff, Wales, United Kingdom

Contact Details

Name: Timothy Eisen

Affiliation: Cancer Research UK

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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