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Spots Global Cancer Trial Database for Combination Hormone Therapy Followed by Radiation Therapy in Treating Patients With Prostate 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: Combination Hormone Therapy Followed by Radiation Therapy in Treating Patients With Prostate Cancer

Official Title: A Randomised Comparison of Short and Protracted Neoadjuvant Hormonal Therapy Prior to Radiation Therapy of High Risk Localized Prostate Cancer

Study ID: NCT00003734

Conditions

Prostate Cancer

Study Description

Brief Summary: RATIONALE: Androgens can stimulate the growth of prostate cancer cells. Hormone therapy using triptorelin and flutamide may fight cancer by reducing the production of androgens. It is not yet known whether giving hormone therapy for 4 months is more effective than giving therapy for 8 months prior to radiation therapy for prostate cancer. PURPOSE: Randomized phase III trial to study the effectiveness of combination hormone therapy for 4 or 8 months followed by radiation therapy in treating patients with prostate cancer.

Detailed Description: OBJECTIVES: I. Compare the efficacy of 4 months vs 8 months of luteinizing hormone-releasing hormone (LHRH) agonist therapy combined with antiandrogen therapy prior to radiotherapy, in terms of disease-free survival and overall survival, in patients with stage I-IV localized invasive prostate cancer. OUTLINE: This is a randomized study. Patients are randomized to one of two treatment arms. All patients receive triptorelin IM once a month and oral flutamide three times daily with meals. Patients randomized to arm I receive this therapy regimen for 4 months. Patients randomized to arm II receive this therapy regimen for 8 months. All patients then undergo radiotherapy 5 days a week for 7 weeks within 2 months of the last injection of triptorelin and within 1 month of the last oral flutamide tablet. Patients are followed every 3 months after radiotherapy. PROJECTED ACCRUAL: A total of 276 patients (138 per treatment arm) will be accrued for this study.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Cork University Hospital, Cork, , Ireland

Letterkenny Hospital, Donnegal, , Ireland

St. Vincent's Hospital, Dublin, , Ireland

Saint Luke's Hospital, Dublin, , Ireland

Mater Misericordiae Hospital, Dublin, , Ireland

Adelaide and Meath Hospital, Dublin, , Ireland

Beaumont Hospital, Dublin, , Ireland

Bon Secours Hospital, Galway, , Ireland

Galway University Hospital, Galway, , Ireland

Regional Hospital - Limerick, Limerick, , Ireland

Sligo General, Sligo, , Ireland

Belfast City Hospital Trust Incorporating Belvoir Park Hospital, Belfast, Northern Ireland, United Kingdom

Contact Details

Name: John Gerard Armstrong, MD, MB, MRCPI

Affiliation: Saint Luke's Hospital

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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