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Spots Global Cancer Trial Database for Goserelin in Preventing Early Menopause in Premenopausal Women Undergoing Chemotherapy for Stage I, Stage II, or Stage III Breast Cancer

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Trial Identification

Brief Title: Goserelin in Preventing Early Menopause in Premenopausal Women Undergoing Chemotherapy for Stage I, Stage II, or Stage III Breast Cancer

Official Title: Ovarian Protection Trial In Premenopausal Breast Cancer Patients [OPTION]

Study ID: NCT00427245

Study Description

Brief Summary: RATIONALE: Goserelin may help prevent early menopause in patients undergoing chemotherapy for breast cancer. It is not yet known whether goserelin is effective in preventing early menopause in women undergoing chemotherapy for breast cancer. PURPOSE: This randomized phase III trial is studying goserelin to see how well it works compared with no goserelin in preventing early menopause in premenopausal women undergoing chemotherapy for stage I, stage II, or stage III breast cancer.

Detailed Description: OBJECTIVES: Primary * Compare the incidence of premature ovarian failure after chemotherapy in premenopausal women with stage I-III breast cancer treated with goserelin vs no goserelin . Secondary * Compare the quality of life of patients treated with these regimens. * Compare menopausal symptoms in patients treated with these regimens. * Compare bone mineral density loss in patients treated with these regimens. * Compare hormone levels in patients treated with these regimens. * Compare menstruation in patients treated with these regimens. * Compare the incidence of pregnancy in patients treated with these regimens. OUTLINE: This is a randomized, open-label, prospective, parallel group, multicenter study. Patients are stratified according to age (≤ 40 years vs \> 40 years) and participating center. Patients are randomized to 1 of 2 treatment arms. Arm I (chemotherapy alone): Patients receive neoadjuvant or adjuvant cyclophosphamide- and/or anthracycline-containing chemotherapy. Treatment continues for 6-8 courses in the absence of disease progression or unacceptable toxicity. Arm II (chemotherapy plus goserelin for ovarian function suppression): Patients receive neoadjuvant or adjuvant chemotherapy as in arm I. Patients also receive goserelin subcutaneously every 3-4 weeks beginning 1-3 weeks before the start of chemotherapy. Treatment with goserelin repeats every 3-4 weeks until completion of chemotherapy. Quality of life is assessed at baseline, at 3, 6, 12, 18, and 24 months, and then annually for up to 5 years. After completion of study therapy, patients are followed periodically for 5 years. Peer Reviewed and Funded or Endorsed by Cancer Research UK PROJECTED ACCRUAL: A total of 400 patients will be accrued for this study.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

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

Royal United Hospital, Bath, England, United Kingdom

Frenchay Hospital, Bristol, England, United Kingdom

Addenbrooke's Hospital, Cambridge, England, United Kingdom

Halton Hospital, Cheshire, England, United Kingdom

Essex County Hospital, Colchester, England, United Kingdom

Dorset County Hospital, Dorchester, England, United Kingdom

Russells Hall Hospital, Dudley, England, United Kingdom

Queen Elizabeth Hospital, Gateshead, England, United Kingdom

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

UCL Cancer Institute, Hampstead, London, England, United Kingdom

Huddersfield Royal Infirmary, Huddersfield, West Yorks, England, United Kingdom

King George Hospital, Ilford, Essex, England, United Kingdom

Ipswich Hospital, Ipswich, England, United Kingdom

Kidderminster Hospital, Kidderminster Worcestershire, England, United Kingdom

Yorkshire Regional Clinical Trials & Research Unit, Leeds, England, United Kingdom

Royal Liverpool University Hospital, Liverpool, England, United Kingdom

Whipps Cross Hospital, London, England, United Kingdom

Newham University Hospital, London, England, United Kingdom

Homerton University Hospital, London, England, United Kingdom

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

Helen Rollason Cancer Care Centre at North Middlesex Hospital, London, England, United Kingdom

Whittington Hospital, London, England, United Kingdom

Guy's Hospital, London, England, United Kingdom

St. George's Hospital, London, England, United Kingdom

Charing Cross Hospital, London, England, United Kingdom

Luton and Dunstable Hospital, Luton-Bedfordshire, England, United Kingdom

Maidstone Hospital, Maidstone, England, United Kingdom

Christie Hospital, Manchester, England, United Kingdom

North Manchester General Hospital - Penine Actute Hospitals Trust, Manchester, England, United Kingdom

Clatterbridge Centre for Oncology, Merseyside, England, United Kingdom

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

Norfolk and Norwich University Hospital, Norwich, England, United Kingdom

Peterborough Hospitals Trust, Peterborough, England, United Kingdom

Dorset Cancer Centre, Poole Dorset, England, United Kingdom

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

Oldchurch Hospital, Romford, England, United Kingdom

Salisbury District Hospital, Salisbury, England, United Kingdom

Scunthorpe General Hospital, Scunthorpe, England, United Kingdom

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

Southampton General Hospital, Southampton, England, United Kingdom

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

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

Warrington Hospital NHS Trust, Warrington, England, United Kingdom

Southend University Hospital NHS Foundation Trust, Westcliff-On-Sea, England, United Kingdom

New Cross Hospital, Wolverhampton, England, United Kingdom

Yeovil District Hospital, Yeovil - Somerset, England, United Kingdom

Aberdeen Royal Infirmary, Aberdeen, Scotland, United Kingdom

Dumfries & Galloway Royal Infirmary, Dumfries, Scotland, United Kingdom

Ninewells Hospital, Dundee, Scotland, United Kingdom

Queen Margaret Hospital - Dunfermline, Dunfermline, Scotland, United Kingdom

Edinburgh Cancer Centre at Western General Hospital, Edinburgh, Scotland, United Kingdom

Falkirk and District Royal Infirmary, Falkirk, Scotland, United Kingdom

Beatson West of Scotland Cancer Centre, Glasgow, Scotland, United Kingdom

Royal Infirmary - Castle, Glasgow, Scotland, United Kingdom

Southern General Hospital, Glasgow, Scotland, United Kingdom

Raigmore Hospital, Inverness, Scotland, United Kingdom

Crosshouse Hospital, Kilmarnock, Scotland, United Kingdom

Royal Alexandra Hospital, Paisley, Scotland, United Kingdom

Bronglais District General Hospital, Aberystwyth, Wales, United Kingdom

Ysbyty Gwynedd, Bangor, Wales, United Kingdom

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

Withybush General Hospital, Haverfordwest, Wales, United Kingdom

Royal Glamorgan Hospital, Lhantrisant, Wales, United Kingdom

Glan Clwyd Hospital, Rhyl, Denbighshire, Wales, United Kingdom

South West Wales Cancer Institute, Swansea, Wales, United Kingdom

Contact Details

Name: Robert C.F. Leonard, MD, BS, MB

Affiliation: Charing Cross Hospital

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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