Decitabine/Cedazuridine and Enzalutamide for the Treatment of Metastatic Castrate Resistant Prostate Cancer

• Status: Not yet recruiting
• Trial end date: 2025-11-15
• Target enrollment: 0
• Participant gender: Male

Summary

This phase Ib trial is to find out the best dose decitabine/cedazuridine and possible benefits and/or side effects of decitabine/cedazuridine and enzalutamide in treating patients with castrate resistant prostate cancer that has spread to other places in the body (metastatic). Chemotherapy drugs, such as decitabine/cedazuridine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Enzalutamide blocks the use of androgen by the tumor cells. Giving decitabine/cedazuridine together with enzalutamide may reverse or help prevent the acquired therapeutic resistance that is observed when enzalutamide is used alone. Drug resistance occurs when cancer cells stop responding to a chemotherapy that had previously been effective.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Roswell Park Cancer Institute
• Collaborator: National Comprehensive Cancer Network
• Treatments: Decitabine

Criteria

Inclusion Criteria:

• Male >= 18 years of age

• Histological or cytological documentation of diagnosis of prostate cancer

• Documented progressive metastatic castrate resistant prostate cancer (mCRPC) based on at least one of the following criteria:

• Prostate specific antigen (PSA) progression defined as 25% increase over baseline value with an increase in the absolute value of at least 2 ng/mL that is confirmed by another PSA level with a minimum of a 1week interval and a minimum PSA of 2 ng/mL

• Soft-tissue progression defined as an increase >= 20% in the sum of the longest diameter (LD) of all target lesions based on the smallest sum LD since treatment started or the appearance of one or more new lesions

• Progression of bone disease (evaluable disease) or (new bone lesion[s]) by bone scan

• Willing to undergo a biopsy, if readily available biopsy site present, i.e., nodal or visceral metastasis (if adequate formalin-fixed paraffin-embedded (FFPE) archival mCRPC samples are not available (or biopsy was taken longer than 6 months from start of study treatment), a fresh pre-treatment mCRPC biopsy needs to be obtained)

• Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1

• Have testosterone < 50 ng/dL. Note: Patients must continue primary androgen deprivation with an luteinising hormone-releasing factor (LHRH) analogue (agonist or antagonist) if they have not undergone orchiectomy

• White blood cells >= 1.5 x 10^9/L (obtained within 14 days prior to treatment start)

• Platelets >= 100 x 10^9/L (obtained within 14 days prior to treatment start)

• Hemoglobin (HGB) >= 9 g/dL (obtained within 14 days prior to treatment start)

• Creatinine clearance > 50 mL/min (obtained within 14 days prior to treatment start)

• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 2.5 x upper limit of normal (ULN (obtained within 14 days prior to treatment start). If the patient has liver metastases, ALT and AST must still be =< 2.5 x ULN. Patients with liver metastases and AST/ALT above this limit will not be enrolled

• Total bilirubin =< 1.5 x ULN; or total bilirubin (TBILI) =< 3.0 x ULN with direct bilirubin within normal range in patients with well documented Gilbert's Syndrome (obtained within 14 days prior to treatment start)

• Ability to swallow and retain oral medication (without crushing, dissolving, or chewing tablets)

• Initial dose escalation/de-escalation: Prior enzalutamide treatment and/or other approved treatments for CRPC for the dose finding phase (determination of MTD) of the study is allowed

• Expansion cohort: Once the MTD has been determined from the dose escalation/de-escalation portion of the study, patient eligibility for the expansion cohort will be genomically driven and will be restricted to metastatic CRPC patients with detectable genomic alterations in RB1 and/or TP53

• Sexually active males must agree to use a condom during intercourse while taking the study drug and for at least 3 months after stopping study treatment. Sexually active males should not father a child during this period. A condom is required to be used by vasectomized men in order to prevent delivery of the drug via seminal fluid. Should a woman become pregnant or suspect she is pregnant while her partner is participating in this study, she should inform her treating physician immediately

• Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure

• NOTE: For blood chemistry labs, Roswell Park clinical blood chemistries are performed on plasma unless otherwise indicated

Exclusion Criteria:

• Participant has a concurrent malignancy or malignancy within 3 years of treatment start, with the exception of adequately treated, basal or squamous cell carcinoma or non-melanomatous skin cancer

• Participant has a known history of human immunodeficiency virus (HIV) infection (testing not mandatory)

• Participant has clinically significant, uncontrolled heart disease and/or recent events including any of the following:

• History of acute coronary syndromes (including myocardial infarction, unstable angina, coronary artery bypass grafting, coronary angioplasty, or stenting) or symptomatic pericarditis within 12 months prior to treatment start

• History of documented congestive heart failure (New York Heart Association functional classification III-IV)

• On screening electrocardiogram (EKG), any of the following cardiac parameters:

bradycardia (heart rate < 50 at rest), tachycardia (heart rate > 90 at rest), PR interval > 220 msec, QRS interval > 109 msec or, corrected QT interval by Fredericia (QTcF) > 450 msec. Congenital long QT syndrome or family history of long QT syndrome

• Patient is currently receiving any of the following medications and cannot be discontinued 7 days prior to treatment start:

• Known strong inducers or inhibitors of CYP3A4/5, including grapefruit, grapefruit hybrids and pummelos, star-fruit and, Seville oranges

• Medications that have a known risk to prolong the QT interval or induce Torsades de Pointes

• Herbal preparations/medications, dietary supplements

• Patient who has received radiotherapy =< 4 weeks prior to start of treatment or limited field radiation for palliation =< 2 weeks prior to treatment start and, who has not recovered to grade 1 or better from related side effects of such therapy (exceptions include alopecia) and/or in whom >= 30% of the bone marrow was irradiated

• Patients with central nervous system (CNS) involvement

• Patients with seizure disorder

• Patient has not recovered from all toxicities related to prior anticancer therapies to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 grade <1 (Exception to this criterion: patients with any grade of alopecia are allowed to enter the study)

• Unwilling or unable to follow protocol requirements

• Participant has any other concurrent severe and/or uncontrolled medical condition that would cause, in the investigator's judgment, an unacceptable safety risk

• Any condition which in the Investigator's opinion deems the participant an unsuitable candidate to receive study drug