Early Phase 1
N=6
Brain Interstitium Temozolomide Concentration Pre and Post Regadenoson Administration
Blood Brain Barrier Defect
Bottom Line
View on ClinicalTrials.gov: NCT02389738 ↗Enrolled (actual)
6
Serious AEs
0.0%
Results posted
Nov 2018
Primary outcome: Primary: Change in AUC0-18 of the Temozolomide Concentration (AUC-T) in Brain Interstitium Before and After Regadenoson Infusion — 19.1; 18.0 percentage of AUC
Study Design & Population
- Study type
- Interventional
- Phase
- Early Phase 1
- Interventions
- Regadenoson (Drug); Temozolomide (Drug); Microdialysis catheter (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- Primary completion
- Feb 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in AUC0-18 of the Temozolomide Concentration (AUC-T) in Brain Interstitium Before and After Regadenoson Infusion |
19.1; 18.0 | — |
| SECONDARY Evaluation of Relationaship Between Cognitive/Mood Disorders and Expression of Biochemical Markers Post-op Day 1 |
— | — |
Summary
The blood-brain barrier (BBB) is an intricate barrier composed of a variety of efflux pumps, a luminal negative charge, a basal lamina and three distinct cell types: brain endothelial cells, pericytes, and astrocyte foot processes. Specifically, the BBB integrity and degree of permeability is regulated by the capillary endothelial cells in response to astrocytic signals. The strength of intercellular junctions (ex. tight junctions, adherins) amongst endothelial cells also plays a major role in permeability. Therefore, modulation of all these paracellular properties may decrease BBB integrity and thus improve drug penetration to the tumor bed. Previous studies utilizing the vasoactive peptide, Regadenoson, demonstrated transient increase in BBB permeability, allowing a 70kD dextran molecule to enter the brain of rodents. Thus, the investigators propose to evaluate brain interstitium concentrations of temozolomide pre and post Regadenoson using brain microdialysis. If Regadenoson successfully demonstrates effectiveness in disrupting the BBB, it could be of major importance in improving the outcome of patients with a variety of brain tumors and other neurologic illnesses.
Eligibility Criteria
Inclusion Criteria
- Age ≥ 18
- Diagnosis of recurrent high grade glioma confirmed by frozen pathology intra-operatively
- Patients with planned surgical debulking or biopsy
- Karnofsky performance status (KPS) ≥ 60%
- Mini Mental Status Exam ≥ 15
- Adequate hepatic function
- Total bilirubin ≤ 1.8 mg/dL
- Serum levels of aspartate aminotransferase ≤ 3x the institutional upper limit of normal
- Adequate renal function
- Serum creatinine ≤ 1.5mg/dL
- Adequate bone marrow function
- ANC ≥ 1500 cells/mm3
- Platelet count ≥ 100,000 cells/mm3
Exclusion Criteria
- Currently receiving chemotherapy, or radiation therapy
- Allergic to temozolomide
- Pregnant or breast-feeding
- Have a serious medical or psychiatric illness or social situation that could interfere with catheter placement or monitoring
- Prior use of VEGF or VEGFR-targeted therapy
- Use of medications: Vincristine, Vinblastine, Rifampin, Opioid's, Antidepressants within the past 24 hours
- Use of investigational agents within the past 4 weeks
- NCI CTC Grade 3 or greater baseline neurologic symptoms
- History of cardiac disease:
- Atrial fibrillation or uncontrolled tachyarrhythmia, or advanced atrioventricular block (second or third degree heart block)
- History of sinus node dysfunction
- History of symptomatic sinus bradycardia or recorded (heart rate 200/110)
- Decompensated or inadequately controlled congestive heart failure.
- Acute pulmonary embolism
- Acute myocarditis or pericarditis
- Acute aortic dissection
- Severe pulmonary hypertension
- Hypertrophic obstructive cardiomyopathy
- Electrolyte abnormalities
- Unexplained chest pain that may be anginal in nature
- Use of sublingual nitroglycerin
- History of Regadenoson hypersensitivity
- Known symptomatic hypotension, uncontrolled hypertension within 30 days
- History of moderate to severe bronchospastic lung disease (including moderate to severe asthma)
- Use of aminophylline in the last 24 hours
- Use methylxanthine or caffeine in the last 12 hours
- Contraindication to adenosine (e.g., bronchoconstrictive/bronchospastic disease)
- Use of potassium supplements or potassium sparing medications in the past 24 hours
- Any patient not deemed medically stable by a physician
- Recent history of illicit drug use (past 3 months)
Data sourced from ClinicalTrials.gov (NCT02389738). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.