Mode
Text Size
Log in / Sign up
Phase 2 N=26 Treatment

A Study of Definitive Therapy to Treat Prostate Cancer

Prostate Cancer

Enrolled (actual)
26
Serious AEs
7.7%
Results posted
Aug 2022
Primary outcome: Primary: Efficacy as Assessed by 2-year PSA Progression-free Survival Rate — 17 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Leuprolide Acetate (Drug); Bicalutamide (Drug); Docetaxel (Drug); Prostatectomy (Procedure); Radiation (Radiation)
Age
Adult, Older Adult · 18+ yrs
Sex
Male
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Primary completion
Apr 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Efficacy as Assessed by 2-year PSA Progression-free Survival Rate
17
SECONDARY
Safety of the Multimodality Therapy as Assessed by Number of Participants With Neutropenia and Surgical or Radiation Toxicities
26
SECONDARY
Time to Prostate-specific Antigen Recurrence
31

Summary

To assess the safety of treating men with oligometastatic prostate cancer with the following therapy: (1st) Systemic chemo-hormonal therapy with up to 6-months (~24 weeks) of neoadjuvant androgen deprivation and up to 6 cycles of chemotherapy, (2nd) definitive local tumor control with prostatectomy +/- adjuvant radiation therapy, and (3rd) consolidative stereotactic radiation to oligometastatic lesions. The men will receive a total of 1 year of androgen deprivation. Androgen blockade will be the same throughout the course of treatment.

Eligibility Criteria

Inclusion Criteria

  • Willing and able to provide written informed consent.
  • Age ≥ 18 years
  • Eastern cooperative group (ECOG) performance status ≤2
  • Documented histologically confirmed adenocarcinoma of the prostate
  • Willing to undergo the following therapy: (1st) Systemic chemo-hormonal therapy with up to 6-months (~24 weeks) of neoadjuvant androgen deprivation and up to 6 cycles of chemotherapy, (2nd) definitive local tumor control with prostatectomy +/- adjuvant radiation therapy, and (3rd) consolidative stereotactic radiation to oligometastatic lesions. Additionally, must be willing to be treated with a full year of androgen deprivation.
  • Oligometastatic prostate cancer: Stage T1-4, N0-1 and/or M1a-b (up to 5 metastatic lesions- including bone lesions and non-regional lymph nodes seen on bone scan, contrast enhanced CT scan, or positron emission tomography scan)
  • Able to swallow the study drugs whole as tablets

Exclusion Criteria

  • Prior local therapy to treat prostate cancer (e.g. radical prostatectomy, radiation therapy, brachytherapy)
  • Prior therapy to a metastatic site.
  • Prior or ongoing systemic therapy for prostate cancer including, but not limited to:
  • Hormonal therapy (e.g. leuprolide, goserelin, triptorelin, degarelix)
  • Cytochrome (CYP) -17 inhibitors (e.g. ketoconazole)
  • Antiandrogens (e.g. bicalutamide, nilutamide)
  • Second generation antiandrogens (e.g. enzalutamide, abiraterone)
  • Immunotherapy (e.g. sipuleucel-T, ipilimumab)
  • Chemotherapy (e.g. docetaxel, cabazitaxel) *Note: may be enrolled if hormone therapy was recently initiated ( upper limit of normal; aspartate aminotransferase , alanine aminotransferase > 2.5 x upper limit of normal)
  • Creatinine clearance of ≥ 30 mL/min. Creatinine clearance should be calculated suing the Cockcroft-Gault formula.
  • Active cardiac disease defined as active angina, symptomatic congestive heart failure, or myocardial infarction within previous six months.
  • Prior history of malignancy in the past 3 years with the exception of basal cell and squamous cell carcinoma of the skin. Other malignancies that are considered to have a low potential to progress may be enrolled at discretion of PI.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02716974). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search