Panitumumab-IRDye800 in Patients With Pancreatic Cancer Undergoing Surgery
A Phase I/II Study Evaluating the Safety and Pharmacokinetics of Panitumumab-IRDye800 as an Optical Imaging Agent to Detect Pancreas Cancer During Surgical Procedures
George Poultsides
27 participants
Feb 7, 2018
INTERVENTIONAL
Conditions
Summary
This phase I/II trial studies the side effects and best dose of panitumumab-IRDye800 and to see how well it works in finding cancer in patients with pancreatic cancer who are undergoing surgery. Panitumumab-IRDye800 is a combination of the antibody drug panitumumab and IRDye800CW, an investigational dye that can be seen using a special camera. Panitumumab-IRDye800 may attach to tumor cells and make them more visible during surgery in patients with pancreatic cancer.
Eligibility
Inclusion Criteria10
- Clinically suspected or biopsy-confirmed diagnosis of pancreatic adenocarcinoma
- Planned standard of care surgery with curative intent for pancreatic adenocarcinoma
- Life expectancy of more than 12 weeks
- Karnofsky performance status of at least 70% or Eastern Cooperative Oncology Group (ECOG)/Zubrod level =\< 1
- Hemoglobin \>= 9 gm/dL
- Platelet count \>= 100,000/mm\^3
- Magnesium \> the lower limit of normal per institution normal lab values
- Potassium \> the lower limit of normal per institution normal lab values
- Calcium \> the lower limit of normal per institution normal lab values
- Thyroid-stimulating hormone (TSH) \< 13 micro international units/mL
Exclusion Criteria7
- Received an investigational drug within 30 days prior to first dose of panitumumab-IRDye800
- Myocardial infarction (MI); cerebrovascular accident (CVA); uncontrolled congestive heart failure (CHF); or unstable angina within 6 months prior to enrollment
- History of infusion reactions to panitumumab or other monoclonal antibody therapies
- Pregnant or breastfeeding
- Evidence of corrected QT (QTc) prolongation on pretreatment electrocardiography (ECG) (greater than 440 ms in males or greater than 460 ms in females)
- Lab values that in the opinion of the physician would prevent surgical resection
- Patients receiving class IA (quinidine, procainamide) or class III (dofetilide, amiodarone, sotalol) antiarrhythmic agents
Interventions
Undergo fluorescence imaging
Given IV
Given IV
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT03384238