Completed

Long Term Adjuvant Hormonal Treatment With LHRH Analogue Versus No Further Treatment in Locally Advanced Prostatic Carcinoma Treated by External Irradiation and a Six Months Combined Androgen Blockade - A Phase III Study

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What is being tested

bicalutamide

+ flutamide

+ triptorelin

DrugRadiation
Who is being recruted

Urogenital Diseases+7

+ Genital Diseases

+ Genital Diseases, Male

See all eligibility criteria
How is the trial designed

Treatment Study

Phase 3
Interventional
Study Start: April 1997
See protocol details

Summary

Principal SponsorEuropean Organisation for Research and Treatment of Cancer - EORTC
Last updated: July 2, 2012
Sourced from a government-validated database.Claim as a partner

Study start date: April 1, 1997

Actual date on which the first participant was enrolled.

OBJECTIVES: Determine the best hormonal scheme to be associated with pelvic radiotherapy in the curative management of prostatic carcinoma for hormonal treatment with regards to treatment outcome (overall survival, clinical disease free survival, local regional control), quality of life (treatment side effects, sexual function), and health economy (cost effectiveness ratio). OUTLINE: This is a randomized, multicenter study. Patients receive external radiation for 5 weeks, followed by a pelvic boost given for 2 weeks and a 6 month combined androgen blockage initiated at the onset of external irradiation. Flutamide (Eulexin) or bicalutamide (Casodex) may be used as the antiandrogens. Antiandrogen treatment starts 1 week before the first injection of triptorelin. Patients are then randomized to one of two treatment arms. Arm I: Patients receive no further treatment. Arm II: Patients receive antiandrogen for 2.5 years plus and LHRH analogue (triptorelin) administered every 3 months. Patients then continue the LHRH analogue alone for an additional 2.5 years in the absence of disease progression. Patients are followed every 6 months for 5 years and then annually thereafter. PROJECTED ACCRUAL: A total of 966 patients will be accrued over 5 years.

NCT00003026
Principal SponsorEuropean Organisation for Research and Treatment of Cancer - EORTC
Last updated: July 2, 2012
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

966 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesGenital DiseasesGenital Diseases, MaleGenital Neoplasms, MaleNeoplasmsNeoplasms by SiteProstatic DiseasesUrogenital NeoplasmsMale Urogenital DiseasesProstatic Neoplasms

Criteria

DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the prostate T1c-T2a-b, N1-2 or pN1-2 (after pelvic lymphadenectomy) T2c-T4, N0-2 Prior external radiotherapy for locally advanced prostatic carcinoma required Prior hormone therapy (6 months of combined androgen blockade) for locally advanced prostatic carcinoma required with PSA no greater than 150 ng/mL before administration No progressive disease after the 6 months of combined androgen blockage No stages T1c/T2a-b with a negative pelvic lymph nodes status that is assessed clinically or surgically No lymph node involvement to common iliac and/or periaortic lymph nodes (M1a) No external iliac lymph node metastasis more than 5 cm in greatest dimension (N3) No distant metastases PATIENT CHARACTERISTICS: Age: Any age Performance status: WHO 0-2 Life expectancy: At least 5 years Hematopoietic: Hemoglobin at least 10 g/dL WBC at least 2,000/mm^3 Platelet count at least 100,000/mm^3 Hepatic: Not specified Renal: Not specified Other: No prior or concurrent cancers other than basal cell skin cancer No serious nonmalignant disease resulting in a life expectancy of less than 5 years PRIOR CONCURRENT THERAPY: Biologic therapy No prior biologic therapy for prostate cancer Chemotherapy No prior chemotherapy for prostate cancer Endocrine therapy See Disease Characteristics Radiotherapy See Disease Characteristics Surgery See Disease Characteristics

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 17 locations

Academisch Ziekenhuis der Vrije Universiteit Brussel

Brussels, BelgiumOpen Academisch Ziekenhuis der Vrije Universiteit Brussel in Google Maps

Institut Jules Bordet

Brussels (Bruxelles), Belgium

Universitair Ziekenhuis Antwerpen

Edegem, Belgium

Universitair Ziekenhuis Gent

Ghent, Belgium
Completed17 Study Centers