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Dexamethasone, Aspirin, and Diethylstilbestrol in Treating Patients With Locally Advanced or Metastatic Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
acetylsalicylic acid
dexamethasone
diethylstilbestrol
Sponsored by
St. Bartholomew's Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring adenocarcinoma of the prostate, stage III prostate cancer, stage IV prostate cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Diagnosis of adenocarcinoma of the prostate Elevated prostate-specific antigen (PSA) Failed previous treatments, including gonadatropan regulatory hormone analogue therapy, radiotherapy, surgery, or any combination of these Biochemically castrate (testosterone < 1 nmol/L) at baseline PATIENT CHARACTERISTICS: Life expectancy ≥ 3 months ECOG performance status 0-3 WBC ≥ 3,000/mm^3 Absolute neutrophil count (neutrophils and bands) ≥ 2,000/mm^3 Platelet count ≥ 50,000/mm^3 Bilirubin ≤ 2 times upper limit of normal (ULN) AST or ALT ≤ 3 times ULN Creatinine ≤ 1.5 times ULN Able to swallow tablets No other malignancy within the past 3 years except basal cell skin cancer No previous thromboembolic disease, including stroke, venous or arterial thrombosis, and myocardial infarction with ongoing angina pectoris Prior uncomplicated myocardial infarction allowed No diabetes mellitus if treatment titration is thought to be difficult or inappropriate No active gastric or duodenal ulcer PRIOR CONCURRENT THERAPY: See Disease Characteristics Prior concurrent bisphosphonates allowed No concurrent investigational agents or participation in another investigational drug study No other concurrent antineoplastic therapy, including new estrogen therapy, radiation therapy, or PC-SPES No other concurrent corticosteroids (e.g., dexamethasone for nausea or vomiting) except those prescribed in the study regimen

Sites / Locations

  • Bristol Haematology and Oncology Centre
  • Burnley General Hospital
  • Kent and Canterbury Hospital
  • Eastbourne District General Hospital
  • Whipps Cross Hospital
  • Saint Bartholomew's Hospital
  • Chelsea Westminster Hospital
  • Maidstone Hospital
  • Milton Keynes General Hospital
  • Churchill Hospital
  • Oldchurch Hospital
  • Torbay Hospital
  • Weston General Hospital
  • Worthing Hospital
  • Cancer Care Centre at York Hospital

Outcomes

Primary Outcome Measures

Prostate-specific antigen (PSA) response

Secondary Outcome Measures

Overall response
Quality of life
Progression-free and overall survival

Full Information

First Posted
April 19, 2006
Last Updated
June 25, 2013
Sponsor
St. Bartholomew's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00316927
Brief Title
Dexamethasone, Aspirin, and Diethylstilbestrol in Treating Patients With Locally Advanced or Metastatic Prostate Cancer
Official Title
A Randomized Phase III Trial of Dexamethasone and Aspirin (DA) Versus Dexamethasone, Diethylstilbestrol and Aspirin (DAS) in Locally Advanced or Metastatic Cancer of the Prostate - Immediate Versus Deferred Diethylstilbestrol
Study Type
Interventional

2. Study Status

Record Verification Date
April 2007
Overall Recruitment Status
Completed
Study Start Date
December 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
St. Bartholomew's Hospital

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Giving dexamethasone together with aspirin and diethylstilbestrol may be effective in lowering prostate-specific antigen levels and may slow or stop the growth of prostate cancer. It is not yet known which schedule of dexamethasone, aspirin, and diethylstilbestrol is more effective in treating prostate cancer. PURPOSE: This randomized phase III trial is studying dexamethasone and aspirin when given together with two different schedules of diethylstilbestrol to compare how well they work in treating patients with locally advanced or metastatic prostate cancer.
Detailed Description
OBJECTIVES: Primary Compare the prostate-specific antigen (PSA) response in patients with locally advanced or metastatic prostate cancer treated with dexamethasone and aspirin with delayed vs immediate diethylstilbestrol. Secondary Compare the overall response rate in patients treated with these regimens. Compare the quality of life of patients treated with these regimens. Compare the progression-free and overall survival of patients treated with these regimens. OUTLINE: This is a randomized, controlled, multicenter study. Patients are stratified according to ECOG performance status (0 vs 1-3), prostate-specific antigen (PSA) response to prior therapy (PSA normalization vs inability to normalize), and bone scan (positive vs negative for bony metastases). Patients are randomized to 1 of 2 treatment arms. Arm I (deferred diethylstilbestrol): Patients receive oral dexamethasone and oral acetylsalicyclic acid once daily (DA). Subsequent to treatment failure with DA, patients continue to receive DA as before in addition to oral diethylstilbestrol once daily (DAS). Treatment with DAS continues in the absence of disease progression or unacceptable toxicity. Arm II (immediate diethylstilbestrol): Patients receive oral dexamethasone, oral acetylsalicyclic acid, and oral diethylstilbestrol once daily (DAS). Treatment continues in the absence of disease progression or unacceptable toxicity. Quality of life is evaluated monthly during study treatment. After completion of study treatment, patients are followed every 3 months for 1 year and then every 6 months thereafter. PROJECTED ACCRUAL: A total of 260 patients will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
adenocarcinoma of the prostate, stage III prostate cancer, stage IV prostate cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Allocation
Randomized
Enrollment
260 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
acetylsalicylic acid
Intervention Type
Drug
Intervention Name(s)
dexamethasone
Intervention Type
Drug
Intervention Name(s)
diethylstilbestrol
Primary Outcome Measure Information:
Title
Prostate-specific antigen (PSA) response
Secondary Outcome Measure Information:
Title
Overall response
Title
Quality of life
Title
Progression-free and overall survival

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Diagnosis of adenocarcinoma of the prostate Elevated prostate-specific antigen (PSA) Failed previous treatments, including gonadatropan regulatory hormone analogue therapy, radiotherapy, surgery, or any combination of these Biochemically castrate (testosterone < 1 nmol/L) at baseline PATIENT CHARACTERISTICS: Life expectancy ≥ 3 months ECOG performance status 0-3 WBC ≥ 3,000/mm^3 Absolute neutrophil count (neutrophils and bands) ≥ 2,000/mm^3 Platelet count ≥ 50,000/mm^3 Bilirubin ≤ 2 times upper limit of normal (ULN) AST or ALT ≤ 3 times ULN Creatinine ≤ 1.5 times ULN Able to swallow tablets No other malignancy within the past 3 years except basal cell skin cancer No previous thromboembolic disease, including stroke, venous or arterial thrombosis, and myocardial infarction with ongoing angina pectoris Prior uncomplicated myocardial infarction allowed No diabetes mellitus if treatment titration is thought to be difficult or inappropriate No active gastric or duodenal ulcer PRIOR CONCURRENT THERAPY: See Disease Characteristics Prior concurrent bisphosphonates allowed No concurrent investigational agents or participation in another investigational drug study No other concurrent antineoplastic therapy, including new estrogen therapy, radiation therapy, or PC-SPES No other concurrent corticosteroids (e.g., dexamethasone for nausea or vomiting) except those prescribed in the study regimen
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonathan Shamash, MD, FRCP
Organizational Affiliation
St. Bartholomew's Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Bristol Haematology and Oncology Centre
City
Bristol
State/Province
England
ZIP/Postal Code
BS2 8ED
Country
United Kingdom
Facility Name
Burnley General Hospital
City
Burnley
State/Province
England
ZIP/Postal Code
BB10 2PQ
Country
United Kingdom
Facility Name
Kent and Canterbury Hospital
City
Canterbury
State/Province
England
ZIP/Postal Code
CT2 3NG
Country
United Kingdom
Facility Name
Eastbourne District General Hospital
City
Eastbourne
State/Province
England
ZIP/Postal Code
BN21 2UD
Country
United Kingdom
Facility Name
Whipps Cross Hospital
City
London
State/Province
England
ZIP/Postal Code
E11 1NR
Country
United Kingdom
Facility Name
Saint Bartholomew's Hospital
City
London
State/Province
England
ZIP/Postal Code
EC1A 7BE
Country
United Kingdom
Facility Name
Chelsea Westminster Hospital
City
London
State/Province
England
ZIP/Postal Code
SW10 9NH
Country
United Kingdom
Facility Name
Maidstone Hospital
City
Maidstone
State/Province
England
ZIP/Postal Code
ME16 9QQ
Country
United Kingdom
Facility Name
Milton Keynes General Hospital
City
Milton Keynes
State/Province
England
ZIP/Postal Code
MK6 5LD
Country
United Kingdom
Facility Name
Churchill Hospital
City
Oxford
State/Province
England
ZIP/Postal Code
OX3 7LJ
Country
United Kingdom
Facility Name
Oldchurch Hospital
City
Romford
State/Province
England
ZIP/Postal Code
RM7 OBE
Country
United Kingdom
Facility Name
Torbay Hospital
City
Torquay Devon
State/Province
England
ZIP/Postal Code
TQ2 7AA
Country
United Kingdom
Facility Name
Weston General Hospital
City
Weston-super-Mare
State/Province
England
ZIP/Postal Code
BS23 4TQ
Country
United Kingdom
Facility Name
Worthing Hospital
City
Worthing
State/Province
England
ZIP/Postal Code
BN11 2DH
Country
United Kingdom
Facility Name
Cancer Care Centre at York Hospital
City
York
State/Province
England
ZIP/Postal Code
Y031 8HE
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
21285990
Citation
Shamash J, Powles T, Sarker SJ, Protheroe A, Mithal N, Mills R, Beard R, Wilson P, Tranter N, O'Brien N, McFaul S, Oliver T. A multi-centre randomised phase III trial of Dexamethasone vs Dexamethasone and diethylstilbestrol in castration-resistant prostate cancer: immediate vs deferred Diethylstilbestrol. Br J Cancer. 2011 Feb 15;104(4):620-8. doi: 10.1038/bjc.2011.7. Epub 2011 Feb 1.
Results Reference
result

Learn more about this trial

Dexamethasone, Aspirin, and Diethylstilbestrol in Treating Patients With Locally Advanced or Metastatic Prostate Cancer

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