Sporadic Angiomyolipomas (AMLs) Growth Kinetics While on Everolimus

Phase 2

Terminated

Conditions: Sporadic Angiomyolipomas (AMLs)

Interventions: Drug: Everolimus

Registration Number: NCT02539459

Lead Sponsor: Fox Chase Cancer Center

Brief Summary: The purpose of this research study is to see if oral everolimus is tolerable and effective in the treatment of sporadic Angiomyolipomas (AMLs). AMLs are the most common non-cancerous tumor of the kidney. They are composed of blood vessels, muscle cells and fat cells.Everolimus is already an approved drug for several other diseases like kidney cancer, but is being studied now specifically to see if it is helpful for people with AML.

Detailed Description: Primary Objective

1. To evaluate the efficacy and tolerability of everolimus in reducing tumor volume in sporadic AMLs as measured by dynamic contrast enhanced magnetic resonance imaging (DCE MRI), in patients who might otherwise be considered for active surgical or percutaneous intervention.

Secondary Objectives

1. To evaluate health-related quality of life (HRQoL) in subjects treated with everolimus for sporadic AMLs.

2. To assess the growth kinetics of sporadic AMLs in patients who have been treated with everolimus as part of the study and demonstrate an objective response as well as those who have been treated with everolimus during the study with a suboptimal or no response.

3. To measure the rate of surgical or percutaneous (embolization) intervention at 1 year from day 1 of study.

4. To assess the safety and tolerability of everolimus in patients with sporadic AML.

Recruitment & Eligibility

Status: TERMINATED

Sex: All

Target Recruitment: 20

Inclusion Criteria

Must have a diagnosis of renal AML > 3 cm confirmed on pre-enrollment Dynamic Contrast Enhanced MRI (DCE-MRI)
Must not have received any prior treatment for AML
Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1
Absolute neutrophil count >= 1,500/ microliter (mcL)
Hemoglobin >=10 g/dL
Platelets >= 100,000/ mcL
international normalized ratio (INR) <= 1.2 X Upper limit Normal (ULN)
activated partial thromboplastin time (aPTT) <= 1.2 X ULN
aspartate aminotransferase (AST) / alanine transaminase (ALT) <= 2.5 X ULN
Total bilirubin <= 2.0mg/dL
Renal Function epidermal growth factor receptor (eGFR) >= 30 mL/min via calculated creatinine clearance
Fasting serum cholesterol <= 300 mg/dL OR <= 7.75 mmol/L AND fasting triglycerides <= 2.5x ULN.

Exclusion Criteria

History of tuberous sclerosis, LAM or any active malignancy
Treatment with any other investigational agents for any other disease
Clinically significant gastrointestinal abnormalities that may increase the risk for gastrointestinal bleeding or affect absorption of investigational product
Active diarrhea of any grade.
History of human immunodeficiency virus (HIV) infection, hepatitis B or C (screening for all three is mandatory prior to study); prior hepatitis C infection
Presence of any active or ongoing infection.
Any known uncontrolled underlying pulmonary disease by history, physical exam or if applicable pulmonary function test (PFTs)
History of certain cardiovascular conditions within the past 6 months
History of Class III or IV congestive heart failure, as defined by the New York Heart Association Classification of Congestive Heart Failure.
History of cerebrovascular accident including transient ischemic attack (TIA), pulmonary embolism or untreated deep venous thrombosis (DVT) within the past 6 months.
Corrected QT interval (QTc) > 480 milliseconds
Poorly controlled hypertension, defined as systolic blood pressure (SBP) of >= 140 millimeters of mercury(mmHg) or diastolic blood pressure (DBP) of >= 90 mmHg.
Evidence of active bleeding or bleeding diathesis
Uncontrolled diabetes mellitus (defined by a Hgb A1c >8) obtained within 14 days prior to registration. Optimal glucose control (Hgb A1c <= 8) must be achieved before registration and monitored during protocol treatment
Any serious and/or unstable pre-existing medical, psychiatric, or other condition that could interfere with subject's safety, provision of informed consent, or compliance to study procedures.
Unable or unwilling to discontinue use of prohibited medications
Concurrent therapy given to treat cancer including treatment with an investigational agent or concurrent participation in another clinical trial involving anti-cancer investigational drug.
Administration of any investigational drug within 30 days or 5 half-lives, whichever is longer, preceding the first dose of study treatment.
Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to everolimus
Prior or current use of systemic anti-vascular endothelial growth factor (VEGF) inhibitors, cytokines or mechanistic target of rapamycin (mTOR) inhibitors (e.g. interferon, interleukin 2).
Pregnant or nursing (lactating) women
Women of child-bearing potential (WOCBP) must use highly effective methods of contraception during the study and 8 weeks after.
Unable to obtain a contrast (gadolinium) based DCE MRI, including include patients with pacemakers, automatic implantable cardioverter/defibrillator (AICDs), non MRI compatible metallic implants or eGFR <30.
Must not have received immunization with an attenuated live vaccine within seven days prior to registration nor have plans to receive such vaccination while on protocol treatment
Must not be taking, nor plan to take while on protocol treatment, strong cytochrome P450 3A4 (CYP3A4) inhibitors, (e.g. ketoconazole, itraconazole, voriconazole, posaconazole, fluvoxamine, nefazodone, nelfinavir, ritonavir) and/or strong CYP3A4 inducers (e.g. phenytoin, rifampin, rifabutin) within 14 days prior to randomization.
History of another primary malignancy, with the exceptions of: non-melanoma skin cancer, and carcinoma in situ of the cervix, uteri, or breast from which the patient has been disease free for >= 3 years
Childs-Pugh A-C liver disease (Appendix II)

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Treatment (everolimus)	Everolimus	Patients will take 10 mg (1 tablet) of everolimus each day for 4 months

Primary Outcome Measures

Name	Time	Method
Number of Patients With Tumor Volume Reduction Greater Than 25%	12 months	Measuring the efficacy and tolerability of everolimus by measuring the number of patients with tumor volume reduction greater than 25% in sporadic AMLs as measured by DCE MRI

Secondary Outcome Measures

Name	Time	Method
Safety and Tolerability of Everolimus in Patients With Sporadic AML	12 months	Number of participants with treatment-related adverse events requiring dose reduction or study withdrawal as assessed by Common Toxicity Criteria for Adverse Effects (CTCAE v4.0)

Trial Locations

Locations (8): Yale School of Medicine
🇺🇸
New Haven, Connecticut, United States
Mayo Clinic
🇺🇸
Rochester, Minnesota, United States
Fox Chase Cancer Center
🇺🇸
Philadelphia, Pennsylvania, United States
Memorial Sloan Kettering
🇺🇸
New York, New York, United States
Dana Farber Cancer Institute
🇺🇸
Boston, Massachusetts, United States
M D Anderson Cancer Center
🇺🇸
Houston, Texas, United States
University of Pennsylvania
🇺🇸
Philadelphia, Pennsylvania, United States
Duke University Health System
🇺🇸
Durham, North Carolina, United States