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Spots Global Cancer Trial Database for Chlorambucil or Fludarabine as First-Line Therapy in Treating Patients With Previously Untreated Waldenström Macroglobulinemia, Splenic Lymphoma, or Lymphoplasmacytic Lymphoma

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Trial Identification

Brief Title: Chlorambucil or Fludarabine as First-Line Therapy in Treating Patients With Previously Untreated Waldenström Macroglobulinemia, Splenic Lymphoma, or Lymphoplasmacytic Lymphoma

Official Title: A Randomised Trial of Chlorambucil Versus Fludarabine as Initial Therapy of Waldenström's Macroglobulinaemia and Splenic Lymphoma With Villous Lymphocytes

Study ID: NCT00608374

Conditions

Lymphoma

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy, such as chlorambucil and fludarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. It is not yet known whether chlorambucil is more effective than fludarabine in treating Waldenström macroglobulinemia, splenic lymphoma, or lymphoplasmacytic lymphoma. PURPOSE: This randomized phase III trial is studying chlorambucil to see how well it works compared with fludarabine as first-line therapy in treating patients with previously untreated Waldenström macroglobulinemia, splenic lymphoma, or lymphoplasmacytic lymphoma.

Detailed Description: OBJECTIVES: * Compare the efficacy of first-line therapy comprising chlorambucil vs fludarabine phosphate in patients with previously untreated Waldenström macroglobulinemia, splenic lymphoma with villous lymphocytes, or non-IgM lymphoplasmacytic lymphoma. OUTLINE: This is a multicenter study. Patients are stratified according to disease (Waldenström macroglobulinemia vs splenic lymphoma with villous lymphocytes vs non-IgM lymphoplasmacytic lymphoma). Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive oral chlorambucil on days 1-10. Treatment repeats every 28 days for up to 12 courses in the absence of disease progression or unacceptable toxicity. * Arm II: Patients receive fludarabine phosphate orally or IV on days 1-5. Treatment repeats every 28 days for 3-6 courses in the absence of disease progression or unacceptable toxicity. Patients undergo quality of life assessment at baseline.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Canberra Hospital, Garran, Australian Capital Territory, Australia

Newcastle Mater Misericordiae Hospital, Waratah, New South Wales, Australia

Princess Alexandra Hospital, Brisbane, Queensland, Australia

Queen Elizabeth Hospital, Woodville, South Australia, Australia

Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia

Stoke Mandeville Hospital, Aylesbury-Buckinghamshire, England, United Kingdom

North Devon District Hospital, Barnstaple, England, United Kingdom

Basingstoke and North Hampshire NHS Foundation Trust, Basingstoke, England, United Kingdom

Royal United Hospital, Bath, England, United Kingdom

City Hospital - Birmingham, Birmingham, England, United Kingdom

Birmingham Heartlands Hospital, Birmingham, England, United Kingdom

Blackpool Victoria Hospital, Blackpool, England, United Kingdom

Royal Bournemouth Hospital, Bournemouth, England, United Kingdom

Bradford Royal Infirmary, Bradford, England, United Kingdom

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

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

Saint Richards Hospital, Chichester, England, United Kingdom

Doncaster Royal Infirmary, Doncaster, England, United Kingdom

Russells Hall Hospital, Dudley, England, United Kingdom

Royal Devon and Exeter Hospital, Exeter, England, United Kingdom

Gloucestershire Royal Hospital, Gloucester, England, United Kingdom

Harrogate District Hospital, Harrogate, England, United Kingdom

Hereford Hospitals, Hereford, England, United Kingdom

Watford General Hospital, Herts, England, United Kingdom

Wycombe General Hospital, High Wycombe, England, United Kingdom

Hull Royal Infirmary, Hull, England, United Kingdom

Queen Elizabeth Hospital, King's Lynn, England, United Kingdom

Leeds General Infirmary, Leeds, England, United Kingdom

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

University College Hospital - London, London, England, United Kingdom

Royal Manchester Children's Hospital, Manchester, England, United Kingdom

Trafford General Hospital, Manchester, England, United Kingdom

Oxford Radcliffe Hospital, Oxford, England, United Kingdom

Derriford Hospital, Plymouth, England, United Kingdom

Pontefract General Infirmary, Pontefract West Yorkshire, England, United Kingdom

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

Rotherham General Hospital, Rotherham, England, United Kingdom

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

Staffordshire General Hospital, Stafford, England, United Kingdom

Taunton and Somerset Hospital, Taunton Somerset, England, United Kingdom

Torbay Hospital, Torquay, England, United Kingdom

Royal Cornwall Hospital, Truro, Cornwall, England, United Kingdom

Kent and Sussex Hospital, Tunbridge Wells, Kent, England, United Kingdom

Sandwell General Hospital, West Bromwich, England, United Kingdom

New Cross Hospital, Wolverhampton, England, United Kingdom

Monklands General Hospital, Airdrie, Scotland, United Kingdom

Southern General Hospital, Glasgow, Scotland, United Kingdom

Pinderfields General Hospital, Wakefield, Scotland, United Kingdom

Ysbyty Gwynedd, Bangor, Wales, United Kingdom

Contact Details

Name: Roger G. Owen, MD, MRCP

Affiliation: Leeds Cancer Centre at St. James's University Hospital

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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