Adjuvant Leuprolide With or Without Docetaxel in High Risk Prostate Cancer After Radical Prostatectomy

NCT ID: NCT00283062

Last Updated: 2012-01-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 228 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-12-31
• Study Completion Date: 2010-12-31

Brief Summary

This is a prospective, multicenter, open-label, randomized phase III study in participants at high risk of recurrent prostate cancer after radical prostatectomy. The study will investigate

• Treatment with docetaxel (TAXOTERE®) every three weeks (q3w) plus leuprolide acetate (ELIGARD®) versus leuprolide acetate alone (ELIGARD®)
• Immediate treatment following prostatectomy versus deferred treatment at the time of relapse

Using a 2x2 factorial design participants will therefore be randomized to

• Immediate adjuvant treatment with docetaxel plus leuprolide acetate (chemotherapy and hormonal therapy)
• Immediate adjuvant treatment with leuprolide acetate alone (hormonal therapy)
• Deferred treatment with docetaxel plus leuprolide acetate (chemotherapy and hormonal therapy)
• Deferred treatment with leuprolide acetate alone (hormonal therapy)

Primary Objective:

• The primary objective of the study is to compare progression-free survival using a 2x2 factorial design

Secondary Objectives:

• To compare the 5-year overall, cancer-specific and metastasis-free survival after systemic treatment between the groups
• To compare the safety and tolerability between Docetaxel in combination with leuprolide acetate and leuprolide acetate alone.
• To evaluate quality of life as measured by the FACT-P questionnaire.

Originally, 1696 participants were planned in the study (with 424 participants randomized to each arm). However, only a total of 211 participants completed the randomization procedure as of 26 September 2007. Thus, sanofi-aventis, in accordance with the Steering Committee, decided to stop the participant recruitment as of 26 September 2007. Participants who had already signed their Informed Consent (IC) before September 26, 2007 were allowed to enter the randomization if they met eligibility criteria. The final revised number of planned participants to be randomly assigned to the 4 treatment arms was 250, and 228 participants were actually randomized.

The final sample size did not allow all the statistical analyses to be conducted on efficacy data. Therefore, the protocol was amended to reflect the change in the plans for statistical analysis. The study was underpowered to serve as the basis for drawing conclusions regarding efficacy and quality of life (QoL) endpoints.

Detailed Description

The study consisted of the following:

• Randomization of eligible participants within 120 days of prostatectomy
• For participants assigned to immediate therapy, a treatment period up to 18 months within 8 days of randomization
• For participants assigned to deferred treatment, a treatment period up to 18 months after evidence of progression prior to December 2010. Participants who did not progress before December 2010 were withdrawn from the study.

Conditions

Prostatic Neoplasms

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: FACTORIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Docetaxel / Leuprolide Acetate - Immediate Treatment (I-CHT)

Participants administered docetaxel every three weeks (q3w) for 6 cycles in combination with leuprolide acetate every 3 months for 18 months immediately following prostatectomy.

Group Type: EXPERIMENTAL

Docetaxel (TAXOTERE®) Chemotherapy

Intervention Type: DRUG

75 mg/m^2 docetaxel administered intravenously over 1 hour on Day 1 every three weeks (q3w) for 6 cycles. The first cycle was to be administered within 8 days after randomization.

Corticosteroid pre-medication was mandatory. The following schedule was recommended - 8 mg Dexamethasone orally for 6 doses given - the night before chemotherapy, the morning of chemotherapy, 1 hour before docetaxel infusion, the night of chemotherapy, the morning of the day after chemotherapy and the night of the day after chemotherapy.

Leuprolide acetate ( ELIGARD®) Hormonal Therapy

Intervention Type: DRUG

22.5 mg leuprolide acetate injection administered subcutaneously (SC) every 3 months for 18 months. The first injection was to be administered within 8 days after randomization.

Leuprolide Acetate - Immediate Treatment (I-HT)

Participants administered leuprolide acetate every 3 months for 18 months immediately following prostatectomy.

Group Type: ACTIVE_COMPARATOR

Leuprolide acetate ( ELIGARD®) Hormonal Therapy

Intervention Type: DRUG

22.5 mg leuprolide acetate injection administered subcutaneously (SC) every 3 months for 18 months. The first injection was to be administered within 8 days after randomization.

Docetaxel / Leuprolide Acetate - Deferred Treatment (D-CHT)

Participants in whom treatment was deferred from randomization until first progression - i.e. PSA progression and/or radiologically or histologically documented progression. Participants were treated with docetaxel every three weeks (q3w) for 6 cycles in combination with leuprolide acetate every 3 months for 18 months.

Group Type: EXPERIMENTAL

Docetaxel (TAXOTERE®) Chemotherapy

Intervention Type: DRUG

75 mg/m^2 docetaxel administered IV over 1 hour on Day 1 q3w for 6 cycles. The first cycle was to be administered within 30 days after progression was confirmed.

Corticosteroid pre-medication was mandatory. The following schedule was recommended - 8 mg Dexamethasone orally for 6 doses given - the night before chemotherapy, the morning of chemotherapy, 1 hour before docetaxel infusion, the night of chemotherapy, the morning of the day after chemotherapy and the night of the day after chemotherapy.

Leuprolide acetate ( ELIGARD®) Hormonal Therapy

Intervention Type: DRUG

22.5 mg leuprolide acetate injection administered subcutaneously (SC) every 3 months for 18 months. The first injection was to be administered within 30 days after progression is confirmed (on Day 1 of docetaxel administration).

Leuprolide Acetate - Deferred Treatment (D-HT)

Participants in whom treatment was deferred from randomization until first progression - i.e. PSA progression and/or radiologically or histologically documented progression. Participants were treated with with leuprolide acetate every 3 months for 18 months.

Group Type: ACTIVE_COMPARATOR

Leuprolide acetate ( ELIGARD®) Hormonal Therapy

Intervention Type: DRUG

22.5 mg leuprolide acetate injection administered subcutaneously (SC) every 3 months for 18 months. The first injection was to be administered within 30 days after progression is confirmed.

Interventions

Docetaxel (TAXOTERE®) Chemotherapy

75 mg/m^2 docetaxel administered intravenously over 1 hour on Day 1 every three weeks (q3w) for 6 cycles. The first cycle was to be administered within 8 days after randomization.

Corticosteroid pre-medication was mandatory. The following schedule was recommended - 8 mg Dexamethasone orally for 6 doses given - the night before chemotherapy, the morning of chemotherapy, 1 hour before docetaxel infusion, the night of chemotherapy, the morning of the day after chemotherapy and the night of the day after chemotherapy.

Intervention Type: DRUG

Leuprolide acetate ( ELIGARD®) Hormonal Therapy

22.5 mg leuprolide acetate injection administered subcutaneously (SC) every 3 months for 18 months. The first injection was to be administered within 8 days after randomization.

Intervention Type: DRUG

Docetaxel (TAXOTERE®) Chemotherapy

75 mg/m^2 docetaxel administered IV over 1 hour on Day 1 q3w for 6 cycles. The first cycle was to be administered within 30 days after progression was confirmed.

Corticosteroid pre-medication was mandatory. The following schedule was recommended - 8 mg Dexamethasone orally for 6 doses given - the night before chemotherapy, the morning of chemotherapy, 1 hour before docetaxel infusion, the night of chemotherapy, the morning of the day after chemotherapy and the night of the day after chemotherapy.

Intervention Type: DRUG

Leuprolide acetate ( ELIGARD®) Hormonal Therapy

22.5 mg leuprolide acetate injection administered subcutaneously (SC) every 3 months for 18 months. The first injection was to be administered within 30 days after progression is confirmed (on Day 1 of docetaxel administration).

Intervention Type: DRUG

Leuprolide acetate ( ELIGARD®) Hormonal Therapy

22.5 mg leuprolide acetate injection administered subcutaneously (SC) every 3 months for 18 months. The first injection was to be administered within 30 days after progression is confirmed.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Participants who met all of the following criteria were considered for enrollment into the study.

• Pathologically confirmed adenocarcinoma of the prostate based on central pathology review. All other variants are excluded
• Randomization should occur less than 120 days after prostatectomy AND lymphadenectomy.
• A predicted probability of 5-year freedom from progression ≤ 60%, as determined by the postoperative nomogram developed by M. Kattan.
• Bone-scan without evidence of metastasis (within 6 months of randomization)
• Chest x-ray without evidence of metastasis (within 6 months of randomization)
• Abdominal computed tomography (CT) Scan without evidence of metastasis (within 6 months of randomization)
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1
• Hematology evaluation within 2 weeks prior to randomization:

• Neutrophils ≥ 2,000/mm3
• Hemoglobin ≥ 10 g/dL
• Platelets ≥ 100,000/mm3
• Hepatic and renal function evaluation within 2 weeks prior to randomization:

• Serum creatinine ≤1.5 × Upper normal limit (UNL) for the institution. If serum creatinine is > 1.5 × UNL, calculate creatinine clearance (should be ≥ 60ml/minute).
• Total serum bilirubin ≤ UNL for the institution. Participants with Gilbert's syndrome may be eligible if indirect serum bilirubin levels at the time of randomization and, at least 6 month prior to randomization, confirm this condition (i.e. elevated indirect serum bilirubin).
• Serum glutamic oxaloacetic transaminase (SGOT) and/or serum glutamic pyruvic transaminase (SGPT) ≤ 1.5 × institutional UNL if alkaline phosphatase is ≤ UNL OR
• alkaline phosphatase ≤ 5 × UNL if SGOT and SGPT are ≤ UNL
• Prostate Specific Antigen (PSA) evaluation within 9 months prior to prostatectomy. However, a 120-day timeframe is recommended
• Post operative PSA necessary for eligibility is defined as a level ≤ 0.2ng/mL using a standard assay at least 30 days after radical prostatectomy and within 7 days prior to randomization. Note that randomization should occur within 120 days after radical prostatectomy
• Serum testosterone ≥ 150ng/dL within 6 months prior to randomization.

Exclusion Criteria

Participants presenting with any of the following will not be included in the study.

• Prior systemic treatment for prostate cancer with hormonal therapy, chemotherapy, or any other anticancer therapy.
• Prior radiation therapy.
• Participants who received, are receiving or scheduled to receive post-operative radiotherapy.
• Participants taking alternative therapies for cancer must stop taking these therapies prior to randomization. Alternative therapies are not allowed during the treatment or follow-up portions of the study. This includes (but is not limited to) alternative therapies such as :

• PC-SPES (all types)
• 5-alpha reductase inhibitors
• Bisphosphonates are to be stopped prior to randomization and are not allowed during the study.
• Chronic treatment with corticosteroids unless initiated > 6 months prior to study entry and at low dose ( ≤ 20 mg methylprednisolone per day or equivalent).
• History of a malignancy other than prostate cancer. Exceptions to these criteria include:

• participants with adequately treated non-melanoma skin cancers, and
• participants with a history of another malignancy that was curatively treated (including participants with superficial bladder cancer) and who have not had evidence of disease for a minimum of 5 years.
• Peripheral neuropathy ≥ Grade 2.
• Electrocardiogram (ECG) with significant abnormalities (as determined by the investigator) within 90 days prior to randomization.
• Participants who are medically unstable, including but not limited to active infection, acute hepatitis, gastrointestinal bleeding, uncontrolled cardiac arrhythmias, interstitial lung disease, inflammatory bowel disease, uncontrolled angina, uncontrolled hypercalcemia, uncompensated congestive heart failure, uncontrolled diabetes, dementia, seizures, superior vena cava syndrome.
• Participants with history of hypersensitivity to polysorbate 80.
• Participants with a known history of viral hepatitis (B, C).

The above information was not intended to contain all considerations relevant to potential participation in a clinical trial.

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jean-Philippe Aussel

Role: STUDY_DIRECTOR

Sanofi

Locations

Sanofi-Aventis Administrative Office

Bridgewater, New Jersey, United States

Sanofi-Aventis Administrative Office

Macquarie Park, , Australia

Sanofi-Aventis Administrative Office

Vienna, , Austria

Sanofi-Aventis Administrative Office

São Paulo, , Brazil

Sanofi-Aventis Administrative Office

Québec, , Canada

Sanofi-Aventis Administrative Office

Paris, , France

Sanofi-Aventis Administrative Office

Frankfurt, , Germany

Sanofi-Aventis Administrative Office

Mumbai, , India

Sanofi-Aventis Administrative Office

Netanya, , Israel

Sanofi-Aventis Administrative Office

Milan, , Italy

Sanofi-Aventis Administrative Office

Col. Coyoacan, , Mexico

Sanofi-Aventis Administrative Office

PE Gouda, , Netherlands

Sanofi-Aventis Administrative Office

Warsaw, , Poland

Sanofi-Aventis Administrative Office

Moscow, , Russia

Sanofi-Aventis Administrative Office

Gauteng, , South Africa

Sanofi-Aventis Administrative Office

Istanbul, , Turkey (Türkiye)

Sanofi-Aventis Administrative Office

Guildford Surrey, , United Kingdom

Countries

United States; Australia; Austria; Brazil; Canada; France; Germany; India; Israel; Italy; Mexico; Netherlands; Poland; Russia; South Africa; Turkey (Türkiye); United Kingdom

Other Identifiers

EudraCT # : 2004-002203-32

Identifier Type: -

Identifier Source: secondary_id

XRP6976J_3501

Identifier Type: -

Identifier Source: org_study_id

NCT00343967

Identifier Type: -

Identifier Source: nct_alias