Hormone Therapy Plus Radiation Therapy in Treating Patients With Prostate Cancer

Prostate Cancer Clinical Trial

Official title:

Phase II Trial of Maximal Androgen Deprivation Followed by Conformal External Beam Radiotherapy With Continued Androgen Deprivation for Clinically Localized Prostate Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00003124
• Other study ID #: CDR0000065883
• Secondary ID: CPMC-IRB-7947NCI
• Status: Completed
• Phase: Phase 2
• First received: November 1, 1999
• Last updated: January 3, 2014
• Start date: May 1997
• Est. completion date: January 2007

Study information

• Verified date: December 2002
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Androgens can stimulate the growth of prostate cancer cells. Hormone therapy using leuprolide and flutamide may fight prostate cancer by reducing the production of androgens. Combining radiation therapy with hormone therapy may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of hormone therapy plus radiation therapy in treating patients with prostate cancer.

Description:

OBJECTIVES:

• Assess the disease free survival of patients with localized adenocarcinoma of the prostate cancer.

• Evaluate the toxic effects of three dimensional conformal external beam radiotherapy and androgen deprivation in these patients.

OUTLINE: Patients are stratified according to PSA values and Gleason scores (class II versus class III/IV).

Patients receive intramuscular leuprolide acetate every 3 months, and oral flutamide tid.

Patients are evaluated on a monthly basis for response. Patients with unchanged or undetectable prostate specific antigen levels are considered to have reached maximal hormonal response and three dimensional conformal external beam radiotherapy is instituted. In addition, patients with disease progression are considered to have reached maximal response, and three dimensional conformal external beam radiotherapy is instituted. Radiotherapy must be administered within 6 months after initiation of leuprolide and flutamide therapy.

Hormonal therapy is administered until 9 months of treatment have elapsed.

Patients will be followed every 3 months for the first year, every 4 months for the second and third years, and every 6 months thereafter.

PROJECTED ACCRUAL: A total of 105 patients will be accrued from biologic class II over 3 years, and 58 patients from biologic class III-IV.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 105
• Est. completion date: January 2007
• Accepts healthy volunteers: No
• Gender: Male
• Age group: N/A and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically proven localized adenocarcinoma of the prostate

• Prostate specific antigen (PSA) greater than 4 or Gleason score at least 8 if PSA is no greater than 4

• CT, MRI, or pelvic lymphadenectomy negative for metastases, if PSA is no greater than 50

• Negative pelvic lymphadenectomy, if PSA is greater than 50

• Bone scan negative for metastases or PSA no greater than 20

PATIENT CHARACTERISTICS:

Age:

• Not specified

Performance Status:

• Not specified

Life Expectancy:

• Not specified

Hematopoietic:

• WBC at least 3,000/mm3

• Platelet count at least 70,000/mm3

• Hemoglobin at least 10 g/dL

• Patients on anticoagulant therapy must have a baseline PT test

Hepatic:

• Bilirubin less than 1.5 times upper limit of normal (ULN)

• ALT or AST less than 1.5 times ULN

• Alkaline phosphatase less than 1.5 times ULN

Renal:

• Creatinine less than 1.5 times ULN

Cardiovascular:

• No history of collagen vascular disease

Other:

• No acute infection requiring antibiotics

• No history of hypersensitivity to flutamide

• No history of hypersensitivity to leuprolide acetate

PRIOR CONCURRENT THERAPY:

Biologic therapy

• Not specified

Chemotherapy

• Not specified

Endocrine therapy

• Not specified

Radiotherapy

• Not specified

Surgery

• Not specified

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Drug:
• flutamide

• leuprolide acetate

Radiation:
• radiation therapy

Locations

Country	Name	City	State
United States	Herbert Irving Comprehensive Cancer Center	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
Herbert Irving Comprehensive Cancer Center	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Heymann JJ, Benson MC, O'Toole KM, Malyszko B, Brody R, Vecchio D, Schiff PB, Mansukhani MM, Ennis RD. Phase II study of neoadjuvant androgen deprivation followed by external-beam radiotherapy with 9 months of androgen deprivation for intermediate- to hig — View Citation