Abi/Pred + ADT vs ADT in PSMA-Positive, Conventionally Node-Negative Prostate Cancer

Official title

Abiraterone/Prednisone + Standard ADT vs Standard ADT for Prostate Cancer Patients With PSMA-Positive Conventional Imaging Negative Pelvic Lymphadenopathy

Overview

The advent of PSMA-PET has improved sensitivity and specificity in staging prostate cancer, particularly in intermediate- and high-risk disease. This has created uncertainty in the management of patients with PSMA-positive but conventionally negative pelvic lymphadenopathy (i.e., \<1 cm in smallest diameter). This study evaluates outcomes of enhanced androgen deprivation therapy (ADT) with abiraterone and prednisone compared to standard ADT, both in combination with radiation therapy, in patients with prostate cancer and PSMA-positive but conventionally negative pelvic lymphadenopathy. A total of 140 eligible participants will be randomized to receive either enhanced ADT with abiraterone and prednisone or standard ADT, both with concurrent radiation therapy. Participants will be followed for 5 years after completion of ADT to assess outcomes. The primary objective is to determine whether enhanced ADT improves 5-year failure-free survival compared to standard ADT. Secondary objectives include evaluation of toxicity, quality of life, biochemical progression-free survival, cancer-specific survival, overall survival, and metastasis-free survival. Exploratory objectives include evaluation of tumor growth and regression rates using PSA values and assessment of the relationship between treatment outcomes and blood-based heme oxygenase-1 (HO-1) levels.

Interventions

• Drug Androgen Deprivation Therapy (ADT)
  Standard hormone therapy used for prostate cancer treatment
• Drug Abiraterone
  Abiraterone administered as part of enhanced androgen deprivation therapy
• Drug Prednisone
  Prednisone administered in combination with abiraterone
• Radiation Radiation Therapy
  Radiation therapy administered per protocol to the prostate and/or pelvic lymph nodes

Primary outcome measures

• 5-year failure-free survival rate [Time frame: From randomization up to 5 years]

Secondary outcome measures (8)

• Toxicity in both arms from 3 months to 2 years post-ADT. [Time frame: From 3 months to 2 years post-ADT]
• Evaluate and compare patient-reported symptom outcomes in both arms from 3 months to 2 years post-ADT. (IPSS) [Time frame: From 3 months to 2 Years post-ADT]
• Evaluate and compare patient-reported symptom outcomes in both arms from 3 months to 2 years post-ADT. (FACT-P) [Time frame: From 3 months to 2 Years post-ADT]
• Evaluate local progression-free survival (i.e., failure-free survival excluding biochemical failure). [Time frame: From randomization up to 5 years]
• Evaluate locoregional progression-free survival (i.e., failure-free survival excluding biochemical failure). [Time frame: From randomization up to 5 years]
• Evaluate 5-year overall survival [Time frame: From randomization up to 5 years]
• Evaluate 5-year cancer-specific survival [Time frame: From randomization up to 5 years]
• Evaluate 5-year metastasis-free survival. [Time frame: From randomization up to 5 years]

Eligibility criteria

Inclusion criteria

• Histopathologically proven diagnosis of local prostate cancer. Biopsies will be confirmed by UNMC pathology review if collected outside our institution.
• Targetable PSMA-avid pelvic lymph node measuring <1cm in short axis diameter.
• No prior definitive treatment or intervention received.
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 within 14 days prior to registration.
• Age ≥ 30 years.
• Patient must be able to provide study-specific informed consent prior to study entry.
• Patient must be able to swallow medications.

Exclusion criteria

• Evidence of distant metastatic disease outside the pelvic lymph nodes (including osseous pelvic disease).
• Presence of any psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule, including alcohol dependence or drug abuse.
• Relative or absolute contraindications to radiation therapy as determined by the treating physician. These include, but are not limited to, inflammatory bowel disease, connective tissue disorders (systemic lupus erythematosus, scleroderma, etc.), and genetic disorders that risk increased sensitivity to radiation therapy.
• Severe, active co-morbidity, defined as follows:

• Unstable angina and/or congestive heart failure requiring hospitalization within the last 3 months prior to registration.
• Congestive heart failure (NYHA functional capacity class II or greater).
• Transmural myocardial infarction within the last 3 months prior to registration.
• History of stroke or transient ischemic attack within 3 months prior to registration.
• Currently uncontrolled diabetes mellitus.
• Ongoing arrhythmias of Grade >2 \[National Cancer Institute's Common Toxicity Criteria for Adverse Events (CTCAE), version 5.03\]; chronic stable atrial fibrillation on stable anticoagulant therapy is allowed.
• Thromboembolic events (e.g., deep vein thrombosis, pulmonary embolism) in the past month.
• Significant vascular disease (e.g., aortic aneurysm, history of aortic dissection) or clinically significant peripheral vascular disease.
• Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration.
• Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration.
• Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects.
• Acquired Immune Deficiency Syndrome (AIDS) based upon the current Centers for Disease Control and Prevention definition that is being treated with contraindicated medications, including but not limited to Atazanavir, Saquinavir, Ritonavir, Indinavir, or Nelfinavir. Note, however, that HIV testing is not required for entry into this protocol. The need to exclude patients with AIDS from this protocol is necessary because the treatments involved in this protocol may be significantly immunosuppressive.
• Uncontrolled seizures or seizures in the past 3 months. Patients can enroll if their seizures have been well-controlled for >3 months on antiseizure medications.
• Gastrointestinal bleeding or any other hemorrhage/bleeding event CTCAE version 5 grade 3 or greater within 30 days prior to registration.
• History of a non-healing wound, ulcer, or bone fracture within 90 days (3 months) prior to registration.
• Total bilirubin ≥1.5X upper limit of normal (ULN) \[except for subjects with Gilbert's disease, in which case total bilirubin not to exceed 10X ULN\], alanine (ALT) and aspartate (AST) aminotransferase >= 2.5X ULN.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Treatment

Study locations

United States · 1 center

• University of Nebraska Medical Center — Omaha

Identifiers

NCT: NCT07237269 · 787-25-FB

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗