Cabozantinib in Combination with Lutetium-177 for the Treatment of Metastatic Castration-Resistant Prostate Cancer, CaboLu Study
This phase Ib trial tests the safety, side effects, and best dose of cabozantinb in combination with lutetium Lu 177 vipivotide tetraxetan (lutetium-177) in treating men with prostate cancer that has spread from where it first started (primary site) to other places in the body (metastatic) and continues to grow and spread despite the surgical removal of the testes or mediation to block androgen production (castration). Cabozantinib binds to and inhibits small receptor tyrosine kinase (RTK), which is overexpressed in a variety of cancer types. Cabozantinib may help shrink tumors by blocking them from growing. Radioactive drugs, such as lutetium-177, may carry radiation directly to tumor cells and not harm normal cells. Giving cabozantinib in combination with lutetium-177 may kill more tumor cells in patients with metastatic castration-resistant prostate cancer.
Inclusion Criteria
- Male subject aged >= 18 years
- Histologically or cytologically confirmed adenocarcinoma of the prostate without small cell histology
- Prior orchiectomy and/or ongoing androgen-deprivation therapy and a castrate level of serum testosterone (< 50 ng/dL or < 1.7 nmol/L)
- Prior treatment with at least one prior novel hormone therapy (NHT), defined as second-generation anti-androgen therapies that include, but are not limited to, abiraterone acetate, enzalutamide, apalutamide, and darolutamide
- Must be eligible for therapy with 177Lu-PSMA-617 and have >= 1 PSMA-positive lesion per treating investigator
- Must have progressive mCRPC per the treating investigator
- Eastern Cooperative Oncology Group (ECOG) performance status =< 2
- Absolute neutrophil count (ANC) >= 1500/uL without granulocyte colony-stimulating factor support
- White blood cell count >= 3000/uL
- Platelet count >= 100,000/uL
- Hemoglobin >= 9g/dL
- Serum albumin >= 2.5 g/dl
- Prothrombin time (PT)/international normalized ratio (INR) or partial thromboplastin time (PTT) test < 1.3x the laboratory upper limit of normal (ULN)
- Total Bilirubin =< 1.5x institutional upper limit of normal (ULN) * For subjects with Gilbert’s disease: =< 3x ULN
- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 3x upper limit of normal (ULN)
- Urine protein/creatinine ratio (UPCR) =< 1 mg/mg (=< 113.2 mg/mmol), or 24-h urine protein =< 1 g
- Estimated creatinine clearance >= 50 mL/min by Cockcroft-Gault formula: * Males: (140−age) x weight (kg) / serum creatinine (mg/dL) x 72
- Sexually active fertile patients and their partners must agree to use medically accepted methods of contraception (e.g., barrier methods, including male condom, female condom, or diaphragm with spermicidal gel) during the course of the study and for 6 months after the last dose of study treatment
- Recovery to baseline or =< grade 1 Common Terminology Criteria for Adverse Events (CTCAE) v5 from toxicities related to any prior treatments, unless adverse events (AE[s]) are clinically nonsignificant and/or stable on supportive therapy
- Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
- Patients must have a life expectancy > 3 months
Exclusion Criteria
- Receiving other investigational anti-cancer agents
- Prior treatment with cabozantinib
- Previous treatment with strontium-89, samarium-153, rhenium-186, rhenium-188, radium-223 or hemi-body irradiation within 6 months prior to randomization
- Previous PSMA-targeted radioligand therapy
- Receipt of any type of small molecule kinase inhibitor (including investigational kinase inhibitor) within 2 weeks before first dose of study treatment
- Receipt of any type of cytotoxic, biologic or other systemic anticancer therapy (including investigational) within 4 weeks before first dose of study treatment
- Radiation therapy for bone metastasis within 2 weeks or any other radiation therapy within 4 weeks before first dose of study treatment
- Systemic treatment with radionuclides within 6 weeks before first dose of study treatment
- Subjects with clinically relevant ongoing complications from prior radiation therapy are not eligible
- Symptomatic cord compression, or clinical or radiologic findings indicative of impending cord compression
- Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/or surgery (including radiosurgery) and stable for at least 4 weeks prior to first dose of study treatment after radiotherapy or at least 4 weeks prior to first dose of study treatment after major surgery (e.g., removal or biopsy of brain metastasis) * Subjects must have complete wound healing from major surgery or minor surgery before first dose of study treatment * Eligible subjects must be neurologically asymptomatic and without corticosteroid treatment at the time of first dose of study treatment
- Major surgery within 4 weeks prior to starting study drug, minor surgery within 10 days, or subjects who have not fully recovered from major surgery
- Any other active malignancy at time of first dose of study treatment or diagnosis of another malignancy within 3 years prior to first dose of study treatment that requires active treatment, with the exception of malignancies with a negligible risk of metastasis or death (e.g., 5-year OS rate > 90%), such as locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the breast
- Concomitant anticoagulation with coumarin agents (e.g., warfarin), direct thrombin inhibitors (e.g., dabigatran), direct factor Xa inhibitor betrixaban, or platelet inhibitors (e.g., clopidogrel). Allowed anticoagulants are the following: * Prophylactic use of low-dose aspirin for cardio-protection (per local applicable guidelines) and low-dose low molecular weight heparins (LMWH) * Therapeutic doses of LMWH or anticoagulation with direct factor Xa inhibitors rivaroxaban, edoxaban, or apixaban in subjects without known brain metastases who are on a stable dose of the anticoagulant for at least 1 week before first dose of study treatment without clinically significant hemorrhagic complications from the anticoagulation regimen or the tumor
- Congestive heart failure New York Heart Association class III or IV, unstable angina pectoris, serious cardiac arrhythmias
- Stroke (including transient ischemic attack [TIA]), myocardial infarction (MI), or other ischemic events, or thromboembolic event (eg, deep venous thrombosis, pulmonary embolism) within 6 months before the first dose of study treatment * Subjects with a diagnosis of incidental, subsegmental pulmonary embolism (PE) or deep vein thrombosis (DVT) within 6 months are allowed if stable, asymptomatic, and treated with a stable dose of permitted anticoagulation (see exclusion criterion 14) for at least 1 week before first dose of study treatment
- Uncontrolled hypertension defined as sustained blood pressure (BP) >= 150 mm Hg systolic or > 90 mmHg diastolic despite optimal antihypertensive treatment
- Gastrointestinal (GI) disorders including those associated with a high risk of perforation or fistula formation: * The subject has evidence of tumor invading the GI tract, active peptic ulcer disease, inflammatory bowel disease (e.g., Crohn’s disease), diverticulitis, cholecystitis, symptomatic cholangitis or appendicitis, acute pancreatitis, acute obstruction of the pancreatic duct or common bile duct, or gastric outlet obstruction * Abdominal fistula, GI perforation, bowel obstruction, or intra-abdominal abscess within 6 months before first dose of study treatment ** Note: Complete healing of an intra-abdominal abscess must be confirmed before first dose of study treatment
- Any other condition that would, in the investigator’s judgment, contraindicate the subject’s participation in the clinical study due to safety concerns or compliance with clinical study procedures (e.g., infection/inflammation, intestinal obstruction, unable to swallow medication, social/ psychological issues, etc.)
- Clinically significant hematuria, hematemesis, or hemoptysis of > 0.5 teaspoon (2.5 ml) of red blood, or other history of significant bleeding (e.g., pulmonary hemorrhage) within 12 weeks before first dose of study treatment
- Cavitating pulmonary lesion(s) or known endotracheal or endobronchial disease manifestation
- Lesions invading or encasing any major blood vessels
- Serious non-healing wound/ulcer/bone fracture
- Uncompensated/symptomatic hypothyroidism
- Moderate to severe hepatic impairment (Child-Pugh B or C)
- Known history of coronavirus disease 2019 (COVID-19) unless the subject has clinically recovered from the disease at least 30 days prior to first dose of study treatment
- Major surgery (e.g., laparoscopic nephrectomy, GI surgery, removal or biopsy of brain metastasis) within 2 weeks before first dose of study treatment or minor surgeries within 10 days before first dose of study treatment * Subjects must have complete wound healing from major surgery or minor surgery before first dose of study treatment * Subjects with clinically relevant ongoing complications from prior surgery are not eligible
- Corrected QT interval calculated by the Fridericia formula (QTcF) > 500 ms per electrocardiogram (ECG) within 14 days before first dose of study treatment * Note: If a single ECG shows a QTcF with an absolute value > 500 ms, two additional ECGs at intervals of approximately 3 min must be performed within 30 min after the initial ECG, and the average of these three consecutive results for QTcF will be used to determine eligibility
- Inability to swallow tablets
- Previously identified allergy or hypersensitivity to components of the study treatment formulations
- Known human immunodeficiency virus (HIV) infection with a detectable viral load within 6 months of the anticipated start of treatment * Note: Subjects on effective antiretroviral therapy with an undetectable viral load within 6 months of the anticipated start of treatment are eligible for this trial
- Active infection including tuberculosis (clinical evaluation that includes clinical history, physical examination, radiographic findings, and tuberculosis [TB] testing in line with local practice), hepatitis B (HBV) (known positive HBV surface antigen [HBsAg] result), or hepatitis C * Note: Subjects with a past or resolved HBV infection (defined as the presence of hepatitis B core antibody [anti-HBc] and absence of HBsAg) are eligible. Subjects positive for hepatitis C (HCV) antibody are eligible only if polymerase chain reaction is negative for HCV ribonucleic acid (RNA)
- Medical, psychiatric, cognitive, or other conditions that may compromise the subject's ability to understand the subject information, give informed consent, comply with the study protocol or complete the study
- Subjects taking prohibited medications. A washout period of prohibited medications for a period of at least five half-lives or as clinically indicated should occur before the start of treatment
Additional locations may be listed on ClinicalTrials.gov for NCT05613894.
Locations matching your search criteria
United States
Utah
Salt Lake City
PRIMARY OBJECTIVES:
I. To determine the maximum tolerated dose (MTD) and recommended dose and schedule for the subsequent expansion stage of daily oral administration of cabozantinib in subjects with metastatic castration-resistant prostate cancer (mCRPC) when taken in combination with 177Lu-prostate-specific membrane antigen (PSMA)-617 (Part 1 [Dose Escalation])
II. To evaluate preliminary efficacy by estimating the progression-free survival (PFS) at 24 weeks (PFS24w) as assessed by per Prostate Cancer Working Group 3 (PCWG3)-modified Response Evaluation Criteria in Solid Tumors (RECIST) version (v)1.1. (Part 2 [Dose Expansion])
SECONDARY OBJECTIVES:
I. To assess the safety and tolerability of 177Lu-PSMA and cabozantinib in the study population (Part 1 [Dose Escalation])
II. To assess the safety and tolerability of 177Lu-PSMA and cabozantinib in the study population (Part 2 [Dose Expansion])
III. To assess the objective response rate (ORR) in the study population (Part 2 [Dose Expansion])
IV. To assess the duration of response (DoR) of the study population (Part 2 [Dose Expansion])
V. To assess the radiographic PFS (rPFS) of the study population (Part 2 [Dose Expansion])
VI. To evaluate PFS at 38 weeks (PFS38w) as assessed by per PCWG3-modified RECIST v1.1 (Part 2 [Dose Expansion])
VII. To assess the prostate-specific antigen (PSA) PFS of the study population (Part 2 [Dose Expansion])
VIII. To assess the PSA 50% response rate in the study population (Part 2 [Dose Expansion])
XI. To assess overall survival (OS) in this study population (Part 2 [Dose Expansion])
EXPLORATORY OBJECTIVES:
I. Association of tumor and blood biomarkers with clinical outcome (Part 1 and 2).
II. Changes in tumor immune infiltration and/or histology or other molecular changes (Part 1 and 2).
OUTLINE: This is a dose-escalation study of cabozantinib followed by a dose-expansion study.
Patients receive cabozantinib orally (PO) once daily (QD) and lutetium-177 intravenously (IV) on day 1 of each cycle. Cycles repeat every 42 days for up to 6 cycles in the absence of disease progression or unacceptable toxicity. Patients may continue to receive cabozantinib PO QD on days 1-21 of subsequent cycles. Patients undergo prostate-specific membrane antigen (PSMA) positron emission tomography (PET) during screening, and computed tomography (CT) or magnetic resonance imaging (MRI), bone scans, tumor biopsies, and blood sample collection throughout the trial.
After completion of study treatment, patients are followed up at 30 days, and then every 3 months for 2 years.
Trial PhasePhase I
Trial Typetreatment
Lead OrganizationHuntsman Cancer Institute/University of Utah
Principal InvestigatorUmang Swami
- Primary IDHCI157278
- Secondary IDsNCI-2023-02087
- ClinicalTrials.gov IDNCT05613894