Survival Outcomes and Tumor Molecular Profile Following Bicalutamide Neoadjuvant Therapy

This study has been completed.
Sponsor:
Information provided by:
University of L'Aquila
ClinicalTrials.gov Identifier:
NCT00418080
First received: January 3, 2007
Last updated: October 5, 2007
Last verified: October 2007

January 3, 2007
October 5, 2007
April 2002
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  • PSA recurrence rate stratified according to treatment modalities
  • EGFR and HER2/neu overexpression rate stratified according to treatment modalities
  • PSA recurrence rate stratified according to EGFR and HER2/neu overexpression levels.
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Complete list of historical versions of study NCT00418080 on ClinicalTrials.gov Archive Site
  • Prostate cancer-specific mortality according to treatment modalities
  • Prostate cancer-specific mortality stratified according to EGFR and HER2/neu overexpression levels.
  • For this purpose a post treatment PSA-doubling time of less than 3 months found following PSA recurrence was considered as a surrogate endpoint for prostate cancer-specific mortality.
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Survival Outcomes and Tumor Molecular Profile Following Bicalutamide Neoadjuvant Therapy
The Role of HER Receptor Family as Indicator of Prognosis and Drug Responsiveness in Locally Advanced Prostate Cancer

As clinical primary endpoints we assessed whether existed differences in:

  1. PSA recurrence rate stratified according to treatment modalities
  2. EGFR and HER2/neu overexpression rate stratified according to treatment modalities
  3. PSA recurrence rate stratified according to EGFR and HER2/neu overexpression levels.

As secondary clinical endpoints we assessed whether existed differences in:

  1. prostate cancer-specific mortality according to treatment modalities
  2. prostate cancer-specific mortality stratified according to EGFR and HER2/neu overexpression levels.

For this purpose a post treatment PSA-doubling time of less than 3 months found following PSA recurrence was considered as a surrogate endpoint for prostate cancer-specific mortality Pre-clinical endpoints As pre-clinical endpoint we assessed whether exist differences in efficacy rate of Bicalutamide and Gefitinib treatment in primary tumor cultures stratified for high and low EGFR and HER2/Neu expression levels. The evaluation of efficacy rate of these treatments was documented by comparing the differences of drugs IC50 values among the groups stratified for EGFR and HER2/Neu levels.

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Interventional
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Treatment
Prostate Cancer
Drug: bicalutamide
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
86
December 2006
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Inclusion Criteria:

  • Patients were eligible if they had histologically confirmed adenocarcinoma of the prostate and the following high-risk features: (1) clinical stage T3a disease with (2) Gleason sum of 7 with a predominant component of 4 (i.e., Gleason 4 + 3 = 7) or (4) Gleason sum of 8, 9 or 10.

Exclusion Criteria:

  • Prior hormonal therapy,
  • Prior radiation,
  • Prior investigational agents,
  • Prior malignancy within the last five years or had any other serious medical or psychiatric condition or illness that would not permit the patient to be managed according to the protocol were excluded.
Male
18 Years to 75 Years
No
Contact information is only displayed when the study is recruiting subjects
Italy
 
NCT00418080
BCLT-1236
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University of L'Aquila
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Principal Investigator: Giovanni Luca Gravina, M.D. University of L'Aquila
University of L'Aquila
October 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP