Neoadjuvant ADT + Darolutamide With Pembrolizumab, Followed by Adjuvant Pembrolizumab in Molecularly Stratified High-Risk Prostate Cancer

Mount Sinai Health System

Status and phase: Not yet enrolling; Phase 2

Conditions: High-risk Prostate Cancer; Prostate Cancer

Treatments: Drug: Pembrolizumab; Drug: Darolutamide; Drug: Lupron

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT07027124

STUDY-23-01400

Details and patient eligibility

About

This is a single-arm, phase II study of neoadjuvant combination therapy of Androgen Deprivation Therapy (ADT), [Gonadotropin-Releasing Hormone (GnRH) agonist Leuprolide], androgen receptor (AR)-antagonist Darolutamide and Pembrolizumab in a stratified high-risk localized prostate cancer cohort, followed by adjuvant treatment with Pembrolizumab (12 cycles) post-radical prostatectomy (RP).

Patients with National Comprehensive Cancer Network (NCCN) high-risk non-metastatic prostate cancer (localized or locally advanced) (defined as Gleason ≥8, disease stage >=cT3a, or PSA l >20 ng/mL) will be risk-stratified at a biopsy using Decipher, a commercial standard-of-care diagnostic assay. Patients satisfying all three criteria of high-risk genomic characteristics listed below as per the Decipher grid results will be enrolled in the study:

1. Decipher Genomic classifier, GC>0.6
2. AR activity score/AR-output gene signature (ARoS)>11.0
3. High Luminal B score/ PAM50 subtype signature

Full description

The objectives of this study are to evaluate if the neoadjuvant ADT, Darolutamide and Pembrolizumab treatment in high-risk prostate cancer patients stratified based on their genomic characteristics will lead to minimum residual disease (MRD).

A total of 40 men ≥ 18 years of age with non-metastatic adenocarcinoma of the prostate, having NCCN high risk localized disease, risk stratified at biopsy based on Decipher score, AR activity score and Luminal B score will be enrolled.

Enrollment: 40 estimated patients

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male Age ≥ 18 years at the time of consent

• Patients must have histopathologically confirmed adenocarcinoma of the prostate

• Patients must have NCCN high-risk localized or locally advanced prostate cancer and absence of distant metastasis or nodal involvement defined as those having one of the following.

  • Gleason score ≥ 8
  • PSA > 20 ng/ml
  • Clinical stage >cT2C (T3a and above)

• Patients must be risk-stratified at biopsy and their cancer should have all three molecular features given below at baseline.

  • Decipher Genomic Classifier >0.6 (interpreted from decipher report)
  • High AR activity/AR activity score >11 (interpreted from decipher report)
  • Luminal B subtype (interpreted from decipher report)

• The patient must have a performance status of 0-1 as determined by criteria set forward by the eastern cooperative oncology group.

• Patients with prior neoadjuvant hormonal therapy are allowed if they meet the following criteria.

  • have completed all treatments ≥ 12, months ago.
  • Recovered from all AEs due to previous therapies.

• If patient has had a major surgery, he should have recovered from all complications and toxicities prior to enrolling in the study.

• Adequate organ and marrow function as defined below:

  • Hematological
  • Absolute neutrophil count (ANC) ≥ 1,500/mcL
  • Platelets ≥ 100,000/mcl
  • Hemoglobin (Hb) ≥ 9 g/dL Hepatic
  • total bilirubin ≤ 1.5 mg/dl (except in patients with gilbert syndrome who can have total bilirubin <3.0 mg/dl)
  • Aspartate aminotransferase (AST) ≤ 2.5 x ULN
  • Alanine aminotransferase (ALT) ≤ 2.5 x ULN Renal
  • Creatinine OR Creatinine ≤ 1.5 ULN OR
  • Calculated creatinine clearance Creatinine clearance ≥ 30 ml/min
  • Men must agree to use a condom and not father a child or donate sperm for the duration of the study and for 90 days after completion of therapy. Subject must agree to partner use of an additional contraceptive method when having intercourse with women of childbearing potential (WOCBP).
  • Ability to understand and the willingness to sign a written informed consent.
  • Participants who are HBs Ag positive are eligible if they have received HBV anti-viral therapy for at least 4 weeks and have undetectable HBV viral load prior to randomization.

Note: Participants should remain on anti-viral therapy throughout study intervention and follow local guidelines for HBV anti-viral therapy post completion of study intervention.

• Hepatitis B screening tests are not required unless:

  • Known history of HBV infection
  • As mandated by local health authority

• Participants with a history of HCV infection are eligible if HCV viral load is undetectable at screening.

Note: Participants must have completed curative anti-viral therapy at least 4 weeks prior to randomization.

• Hepatitis C screening tests are not required unless:

  • Known history of HCV infection
  • As mandated by local health authority

• Participants with a known history of Human immunodeficiency virus (HIV) infection are eligible as long as they have an undetectable viral. HIV positive participants must be taking stable ART for ≥ 12 weeks and have an undetectable HIV viral load within 28 days before enrollment. Minor fluctuations up to 200 copies/mL are acceptable.

Exclusion criteria

• Patients with metastatic disease

• Patients with Gleason score <8

• Patients with Biopsy Decipher score ≤0.6.

• Patients have had prior hormonal therapy (please see inclusion criteria for exceptions).

• Patients have had prior radiation therapy or chemotherapy for prostate cancer.

• Patients with active cardiac disease defined as having any of the following within 6 months prior to the start of treatment:

  • myocardial infarction,
  • severe/unstable angina pectoris,
  • congestive heart failure,
  • hospitalization for any cardiac event

• Patients has active GI disorder that will interfere with absorption of study drug Darolutamide Subject has prior treatment with androgen receptor inhibitors, such as apalutamide, Darolutamide, enzalutamide, abiraterone acetate or other investigational CYP17 inhibitor.

• Inability to swallow oral medications.

• Patients has active infection requiring systemic therapy within 7 days of Week 1.

• Patients has received prior therapy with anti-PD1, anti-PDL1, anti-PDL2 or with other checkpoint inhibitors or T-cell costimulatory/inhibitory agents (e.g., CD137, OX-40, CTLA4).

• Patients with an active viral Hepatitis B (defined as Hepatitis B surface antigen [HBsAg] reactive or detectable [qualitative] Hepatitis b virus [HBV] DNA or defined as Hepatitis V virus [HCV] ribonucleic acid [RNA] [qualitative] is detected), known Human Immunodeficiency virus (HIV) infection with detectable viral load, or chronic liver disease with a need of treatment.

• Patients has a known active or known history of TB (Bacillus tuberculosis) or active history of non-infectious pneumonitis.

• Patients who are immunodeficient or are receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days of study intervention. Topical or inhaled steroids are permitted in absence of immunodeficiency or autoimmune disease.

• Patients have active auto-immune disease that has required systemic therapy (use of disease modifying agents, corticosteroids, or immunosuppressive drugs) in the past 2 years. However, subjects receiving replacement therapy (e.g., insulin, thyroxine, or physiological corticosteroid replacement therapy for adrenal and pituitary insufficiency) are eligible.

• Has history or current evidence of any condition, therapy that might confound results of the study. - Has known psychiatric, epileptic or substance abuse history or disorder that would interfere with participant's ability to cooperate with the requirements of the study.

• Patients with known brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.

• Known history of allergic reactions attributed to compounds of similar chemical or biologic composition to Agent(s) or other agents used in study.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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40 participants in 1 patient group

Participants with Prostate Cancer

Experimental group

Description:

Neoadjuvant ADT plus AR- antagonist, Darolutamide plus Pembrolizumab (5 cycles) prior to radical prostatectomy (RP) in a stratified high-risk localized prostate cancer cohort, followed by adjuvant treatment with Pembrolizumab (12 cycles) post-RP.

Treatment:

Drug: Lupron

Drug: Darolutamide

Drug: Pembrolizumab