A Pilot Study of F-18 Paclitaxel (FPAC) PET for Evaluating Drug Delivery of Solid Tumors in Breast, Lung, Renal, and Adrenal Cancers
Background: * Paclitaxel is a chemotherapy drug that is commonly used to treat different types of cancers. However, cancer tumors can become resistant to paclitaxel, and as a result they will fail to accumulate sufficient concentrations of paclitaxel to kill the cancer cells. Researchers are interested in studying whether tumors have become resistant to paclitaxel, but to do so it must be possible to see how much paclitaxel is absorbed by the tumor cells. * 18F-Fluoropaclitaxel (FPAC) is a form of paclitaxel that has been modified to be slightly radioactive in order to show up on positron emission tomography (PET) scans. By injecting a very small amount (much less that that used to treat tumors) of the radiolabeled drug into the body, researchers hope to use PET scans to evaluate the amount of the drug absorbed by solid tumors. Because FPAC is best used to study tumors located above the diaphragm, all subjects in the study will have tumors near or above the diaphragm. Objectives: \- To determine the safety and effectiveness of FPAC as a radiological evaluation chemical. Eligibility: \- Individuals at least 18 years of age who have been diagnosed with breast, adrenal, renal, or lung cancer and have a tumor located someone in the body at least 1 centimeter above the diaphragm. Design: * Participants will be screened with a physical exam, blood tests, and imaging studies as directed by the study researchers. * Participants will receive a single dose of FPAC, followed by a series of PET scans. Regular scans will be performed for 3 hours after the dose of FPAC. * Participants will also have a single dose of a more conventional radiotracer, followed by a series of PET scans. The results of the two sets of scans will be compared with information from previous imaging studies of participants' tumors.
Checked against the public recordLast updated Dec 17, 2019 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Diagnostic
- Study type
- Interventional
- Phase
- Early Phase 1
- Sponsor
- National Cancer Institute (NCI)
- Interventions being studied
- Drug: FPAC
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
* INCLUSION CRITERIA: * Subjects must have a history of histologically or cytologically confirmed breast, lung, adrenal or renal cancer with a tumor above the diaphragm greater than or equal to 1 cm * Subjects must be 18 years or older for inclusion in this study. * Subjects must sign a written informed consent document and in accordance with institutional guidelines. * If female, the subject must be postmenopausal for a minimum of two years, be surgically sterile, or have a negative pregnancy test within the 24 hours prior to tracer injection * There are no study related limitations regarding previous radiation or chemotherapy. * Subjects must have an ECOG performance status less than or equal to 2 (Karnofsky greater than or equal to 60%) * Subjects must have normal organ and marrow function as defined below: * leukocytes greater than or equal to 3,000/mcL * absolute neutrophil count greater than or equal to 1,500/mcL * platelets greater than or equal to 100,000/mcL * total bilirubin within less than or equal to 2.5 times institutional limits OR \< 3.0 mg/dl in patients with Gilbert s syndrome * AST(SGOT)/ALT(SGPT) less than or equal to 2.5 times the institutional upper limit of normal (\<5 times the ULN for patients with known hepatic metastases) * When applicable, a documented history of prior chemotherapy and radiation therapy and responses to those treatments must be available. EXCLUSION CRITERIA: * Subjects may not receive any other investigational agents 24 hours prior to or following FPAC injection * Subjects must NOT receive radiation therapy to the target lesion less than or equal to 8 weeks prior to FPAC injection * Subjects must NOT have had surgery near the target lesion less than or equal to 4 weeks prior to FPAC injection * Subjects with a history of allergic reactions attributed to compounds of similar chemical or biologic composition to F-18 fluoropaclitaxel (i.e. Taxol) * Subjects with severe claustrophobia (not relieved by oral anxiolytics) or other condition that would make them unable to lie still for the duration of the study * Subjects with uncontrolled intercurrent illness or psychiatric illness/social situations that would limit compliance with study requirements * Subjects who are pregnant or lactating or who suspect they might be pregnant. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with FPAC, breastfeeding should be discontinued if the mother receives FPAC.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- National Institutes of Health Clinical Center, 9000 Rockville PikeBethesda, Maryland
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Dec 17, 2019. Always confirm current availability with the study team.