Clinical Trials /

A Trial of Androgen Deprivation, Docetaxel, and Enzalutamide for Metastatic Prostate Cancer

NCT03246347

Description:

This is a study with the combination of androgen deprivation therapy (ADT) and docetaxel with the addition of enzalutamide in the treatment of subjects with metastatic prostate cancer. The purpose of this study is to assess if ADT + docetaxel + enzalutamide is well tolerated and demonstrates improved efficacy compared to ADT + docetaxel.

Related Conditions:
  • Prostate Adenocarcinoma
Recruiting Status:

Recruiting

Phase:

Phase 2

Trial Eligibility

Document

Title

  • Brief Title: A Trial of Androgen Deprivation, Docetaxel, and Enzalutamide for Metastatic Prostate Cancer
  • Official Title: A Phase II Trial of Androgen Deprivation, Docetaxel and Enzalutamide in Patients With Metastatic Hormone Sensitive Prostate Cancer

Clinical Trial IDs

  • ORG STUDY ID: LCI-GU-PRO-ADDE-001
  • SECONDARY ID: 00018087
  • NCT ID: NCT03246347

Conditions

  • Prostate Cancer
  • Prostate Adenocarcinoma

Interventions

DrugSynonymsArms
ADT+Docetaxel+EnzalutamideTaxotere, XtandiSingle Arm

Purpose

This is a study with the combination of androgen deprivation therapy (ADT) and docetaxel with the addition of enzalutamide in the treatment of subjects with metastatic prostate cancer. The purpose of this study is to assess if ADT + docetaxel + enzalutamide is well tolerated and demonstrates improved efficacy compared to ADT + docetaxel.

Detailed Description

      This is a single center, single arm, phase II trial designed to evaluate the 12 month PSA
      complete response rate in patients with metastatic hormone sensitive prostate cancer treated
      with ADT, docetaxel and enzalutamide. The primary endpoint of this study will be 12-month PSA
      complete response rate, which will be assessed against a contemporary historical control rate
      for the combination of ADT and docetaxel alone in the metastatic hormone naive setting. The
      study will be conducted at all participating sites across North and South Carolina within the
      Levine Cancer Institute network. Enrollment is anticipated to be completed within 24 months.
    

Trial Arms

NameTypeDescriptionInterventions
Single ArmExperimentalDocetaxel + Enzalutamide + Androgen Deprivation Therapy
  • ADT+Docetaxel+Enzalutamide

Eligibility Criteria

        Inclusion Criteria:

          -  Histologically or cytologically confirmed adenocarcinoma of the prostate without
             evidence of small cell carcinoma or greater than 50% neuroendocrine differentiation.
             Metastatic disease must be present including soft tissue, and/or bone metastases OR
             nonregional lymph node involvement prior to study enrollment. If the subject has
             regional lymph node involvement, there must be at least one additional site of disease
             including visceral, non-regional nodal or skeletal metastases.

          -  ADT with surgical castration with bilateral orchiectomy or medical castration with
             LHRH agonist or LHRH antagonist therapy may have been initiated no greater than 112
             days (16 weeks) prior to enrollment date. Subjects who initiated ADT prior to consent,
             are not eligible if PSA has risen ≥ 25% and ≥ 2 ng/ml above nadir value since
             initiation of ADT prior to consent.

          -  At least one PSA level of ≥ 5 ng/ml within 90 days prior to consent.

          -  Prior ADT for non-metastatic disease with LHRH agonist or LHRH antagonist therapy in
             the neoadjuvant/adjuvant setting is permitted if:

               1. Total duration of therapy did not exceed 36 months

               2. 6 months have elapsed since completion of therapy prior to consent,

               3. Serum testosterone > 50 ng/dl within 28 days prior to reinitiation of ADT for
                  metastatic disease

               4. Prior ADT for non-metastatic disease must have accompanied definitive local
                  therapy for curative intent.

          -  Age ≥ 18 years.

          -  ECOG performance status 0-2.

          -  Adequate liver function: AST and ALT <1.5x upper limit of normal, total bilirubin < 1x
             upper limit of normal.

          -  Adequate bone marrow function: Platelets >100,000 cells/mm3, Hemoglobin > 8.0g/dL and
             ANC > 1,500 cells/mm3.

          -  Adequate renal function with a creatinine clearance (based on Cockcroft-Gault formula)
             ≥ 30 mL/min.

          -  Ability to understand and the willingness to sign a written informed consent document.

          -  Able to swallow and retain oral medication

        Exclusion Criteria:

          -  Personal history of seizure.

          -  Personal history of conditions that may predispose to seizure activity including
             cortical cerebrovascular accident or brain trauma.

          -  Known central nervous system metastases, including involvement of brain parenchyma and
             leptomeninges.

          -  Personal history of any condition that may impair absorption of enzalutamide.

          -  Prior or current therapy with ketoconazole, abiraterone, enzalutamide, apalutamide
             (ARN-509, JNJ-56021927), darolutamide (ODM-201, BAY1841788) or cytotoxic chemotherapy
             such as docetaxel, cabazitaxel, cyclophosphamide.

          -  Prior therapy with bicalutamide, nilutamide or flutamide within 14 days of enrollment.

          -  Within 28 days of major surgery and/or lack of recovery from prior surgical procedure
             or 14 days of palliative radiation prior to enrollment.

          -  Prior or current therapy with an investigational agent for metastatic prostate cancer.

          -  Known hypersensitivity to drugs formulated with polysorbate 80.

          -  Personal history of posterior reversible encephalopathy syndrome.

          -  CTCAE version 4.0 grade 2-4 peripheral sensory neuropathy.

          -  Human immunodeficiency virus infection or active hepatitis B or C infection.

          -  Uncontrolled and current illness including, but not limited to, ongoing or active
             infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
             arrhythmia, or psychiatric illness/social situations that would limit compliance with
             study requirements in the opinion of the investigator.

          -  Presence of any of the following within the previous 3 months prior to enrollment:
             myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass
             graft, congestive heart failure, or cerebrovascular accident including transient
             ischemic attack.

          -  History of an additional active malignancy within 12 months prior to the date of
             consent (except non-melanoma skin cancer).

          -  Current use of strong CYP2C8 inhibitors, CYP3A4 inducers or CYP3A4, CYP2C9 or CYP2C19
             substrates with a narrow therapeutic range as listed in Section 7.2.1.

          -  Any condition that requires the use of prednisone > 10mg daily, or equivalent daily
             glucocorticoid dose, for greater than 14 days
      
Maximum Eligible Age:N/A
Minimum Eligible Age:18 Years
Eligible Gender:Male
Healthy Volunteers:No

Primary Outcome Measures

Measure:PSA complete response rate
Time Frame:12 month
Safety Issue:
Description:

Secondary Outcome Measures

Measure:Serologic response rate
Time Frame:Duration of study participation, an average of 2 years
Safety Issue:
Description:
Measure:Radiographic response rate
Time Frame:Duration of study participation, an average of 2-3 years
Safety Issue:
Description:
Measure:Time to castrate resistance
Time Frame:Duration of study participation, an average of 2 years
Safety Issue:
Description:
Measure:serologic progression free survival
Time Frame:Duration of study participation, an average of 2 years
Safety Issue:
Description:
Measure:radiographic progression free survival
Time Frame:Duration of study participation, an average of 2-3 years
Safety Issue:
Description:
Measure:overall survival
Time Frame:Duration of study participation, an average of 5 years
Safety Issue:
Description:
Measure:time to treatment failure
Time Frame:Duration of study participation, an average of 2-3 years
Safety Issue:
Description:
Measure:Treatment-related adverse events as assessed by CTCAE v4.0
Time Frame:Duration of study participation, an average of 5 years
Safety Issue:
Description:

Details

Phase:Phase 2
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:Earle Burgess

Last Updated

August 12, 2019