Study of OGX-011 Given Prior to Radical Prostatectomy in Patients With Localized Prostate Cancer

Prostate Cancer Clinical Trial

Official title:

A Phase II Study of OGX-011 Given Prior to Radical Prostatectomy in Patients With Localized Prostate Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00138918
• Other study ID #: R04-0092
• Status: Completed
• Phase: Phase 2
• First received: August 26, 2005
• Last updated: March 1, 2017
• Start date: June 2005
• Est. completion date: May 13, 2008

Study information

• Verified date: March 2017
• Source: University of British Columbia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this trial is to assess the effects of combined therapy with androgen ablation and OGX-011 (an antisense to clusterin) given prior to radical prostatectomy on pathologic complete response rates in men with localized prostate cancer and high risk features.

Description:

Clusterin as an anti-apoptotic cytoprotective chaperone protein upregulated in an adaptive cell survival manner that confers resistance to various cell death triggers, including hormone-, radiation-, and chemotherapy. In pre-clinical models, inhibition of clusterin expression using the second generation antisense OGX-011 can enhance cell death following treatment with androgen ablation, radiotherapy, and chemotherapy. In phase I clinical trials, OGX-011 has been well tolerated and a biologically effective dose has been identified in humans.

Study Design

This is an open-label, non-blinded, phase II clinical, tissue pharmacokinetic and pharmacodynamic study of weekly OGX-011 and neoadjuvant hormone therapy prior to radical prostatectomy in patients with localized prostate carcinoma and high-risk features.

Study Objectives

Primary Objectives

• To assess the effects of combined neoadjuvant hormone therapy (NHT) and OGX-011 prior to radical prostatectomy on pathologic complete response rates in men with high risk localized prostate cancer.

Secondary Objectives

• To quantify changes in clusterin expression in residual prostate cancer after treatment with NHT and OGX-011.

• To measure levels of full length OGX-011 in prostate tissues after 3 months of NHT.

• To assess the safety and tolerability toxicity of 3 months of OGX-011 and NHT prior to radical prostatectomy.

• To measure evidence of OGX-011's effect on clusterin expression in patient peripheral blood mononuclear cells (PBMNC).

• To measure evidence of OGX-011's effect on patient clusterin serum levels.

• To assess the effects of combined NHT and OGX-011 on time to PSA nadir.

• To determine PSA recurrence rates after combined NHT and OGX-011.

Key Eligibility Criteria

1. Histologically confirmed adenocarcinoma of the prostate, previously untreated

2. Potential candidate for radical prostatectomy

3. Any one of the following criteria (minimum of 2 positive biopsies):

• Clinical stage T3

• Serum PSA > 10 ng/ml

• Gleason score 7-10

• Gleason score 6 and > 3 positive biopsies

4. ECOG performance status 0-1

5. WBC ≥ 3.0 x 10^9/L

6. Hemoglobin ≥ 100 g/L

7. Platelets ≥ 100 x 10^9/L

8. PTT, INR, AST, ALT, creatinine, total bilirubin within normal limits

Treatment Plan

Approximately 45 newly diagnosed, previously untreated patients with clinically localized, high-risk prostate carcinoma will be entered into this trial. These patients will receive neoadjuvant hormone therapy (buserelin 9.9 mg subcutaneously x 1 injection with flutamide 250 mg orally T.I.D. for the first 4 weeks only) for 12 weeks in combination with OGX-011 (a 2'MOE phosphorothioate clusterin antisense oligonucleotide) weekly on a 4 week cycle for 3 courses. For week one, cycle one only, OGX-011 will be given on Days 1, 3 and 5. OGX-011 is given at a dose of 640 mg by intravenous infusion over 2 hours. Radical prostatectomy will take place within 14 days of the last dose of OGX-011.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: May 13, 2008
• Est. primary completion date: May 13, 2008
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Histologically confirmed adenocarcinoma of the prostate, previously untreated

2. Males = 18 years of age.

3. Potential candidate for radical prostatectomy

4. Any of the following (minimum of 2 positive biopsies):

• Clinical stage T3

• Serum PSA > 10 ng/ml

• Gleason score 7-10

• Gleason score 6 and > 3 positive biopsies

5. ECOG performance status 0-1

6. WBC = 3.0 x 10^9/L

7. Hemoglobin = 100 g/L

8. Platelets = 100 x 10^9/L

9. PTT, INR, AST, ALT, creatinine, total bilirubin within normal limits

10. Patients must sign an informed consent that complies with US Regulations (US 21 Code of Federal Regulations [CFR]) and the International Conference on Harmonization (ICH) Guideline for Good Clinical Practice (GCP) prior to undergoing treatment.

Exclusion Criteria:

1. Prior hormone, radiation, or chemotherapy for prostate cancer

2. Evidence of active infection

3. Patients receiving therapeutic doses of warfarin or heparin

4. Severe end organ disease

5. Patients who otherwise would not be candidates for radical prostatectomy because of health or tumour factors

6. Patients will be excluded if they had any prior malignancy unless the prior malignancy was diagnosed and definitively treated at least five years previously and there has never been any evidence of recurrence.

7. Other serious illness, psychiatric, or medical condition that would not permit the patient to be managed according to the protocol.

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Biological:
• OGX-011
See Detailed Description, Treatment Plan

Locations

Country	Name	City	State
Canada	BC Cancer Agency and Vancouver General Hospital	Vancouver	British Columbia

Sponsors (2)

Lead Sponsor	Collaborator
University of British Columbia	United States Department of Defense

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To assess the effects of combined neoadjuvant hormone therapy (NHT) and OGX-011 prior to radical prostatectomy on pathologic complete response rates in men with high risk localized prostate cancer		See Detailed Description, Treatment Plan
Secondary	To quantify changes in clusterin expression in residual prostate cancer after treatment with NHT and OGX-011		See Detailed Description, Treatment Plan
Secondary	To measure levels of full length OGX-011 in prostate tissues after 3 months of NHT		See Detailed Description, Treatment Plan
Secondary	To assess the safety and tolerability toxicity of 3 months of OGX-011 and NHT prior to radical prostatectomy		See Detailed Description, Treatment Plan
Secondary	To measure evidence of OGX-011's effect on clusterin expression in patient peripheral blood mononuclear cells (PBMNC)		See Detailed Description, Treatment Plan
Secondary	To measure evidence of OGX-011's effect on patient clusterin serum levels		See Detailed Description, Treatment Plan
Secondary	To assess the effects of combined NHT and OGX-011 on time to prostate specific antigen (PSA) nadir		See Detailed Description, Treatment Plan
Secondary	To determine PSA recurrence rates after combined NHT and OGX-011		See Detailed Description, Treatment Plan