F-Tryptophan PET/CT in Human Cancers

Trial Title: F-Tryptophan PET/CT in Human Cancers

NCT ID: NCT05556473

Condition: Intracranial Glioma
Metastatic Brain Tumor
Breast Cancer
Neuroendocrine Tumors
Rectal Cancer

Conditions: Official terms:
Neuroendocrine Tumors
Tryptophan

Study type: Interventional

Study phase: Phase 1

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Diagnostic

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: 1-(2-[18F]FLUOROETHYL)-L-Tryptophan
Description: Radioactive tracer 1-(2-[18F]FLUOROETHYL)-L-Tryptophan 0.14mCi/kg/5MBq/kg injection given one time prior to PET Scan.
Arm group label: [18F]FETrp PET radiotracer

Other name: [18F]FETrp PET radiotracer

Summary: Imaging procedures such as 1-(2-[18F]FLUOROETHYL)-L-Tryptophan PET/CT in patients with cancers may help doctors assess a patient's response to treatment and help plan the best treatment in the future. The purpose is to see if there can be a better differentiation of tumor and non-tumor tissue where the tumor tissue has a higher uptake of Tryptophan.

Detailed description: In this research study, we will compare the uptake of the tracer on F-Tryp PET/CT in patients with cancers; specifically, to evaluate whether the tumors show increased tracer uptake as compared to non-tumor tissues, using F-Tryp PET/CT. Additionally, we will evaluate the biodistribution (i.e. track where the tracer has traveled in the body) and radiation dosimetry (i.e., absorbed dose of tracer in tissue). These changes may be compared with results of the physical examination and scans (CT and MRI or standard clinical PET) that are done as part of routine clinical care or as part of other studies. Pictures (images) from the PET scan will be made showing the distribution throughout the body of substances containing a small amount of radioactive material.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Age ≥18 years. - Targeted lesion (tumor) is at least 1 cm in diameter as shown by clinical imaging. - Patient is able to lie in the PET/CT scanner for at least 70 minutes while undergoing scanning. - Women of childbearing potential must not be pregnant or breastfeeding. - Recent anatomic imaging with visible disease (tumor) for comparison with the PET/CT. . - Physical exam within 28 days of PET imaging, CBC and Multiphasic (including electrolytes, BUN, creatinine, total bilirubin, AST and ALT) within 14 days. - Patients must sign an informed consent indicating that they are aware of the investigational nature of this study. Inclusion Criteria Specific for Intracranial Tumors - Clinical and MRI diagnosis of an intracranial lesion suspicious for a brain tumor, including gliomas or metastatic brain tumors; primary, residual, or recurrent brain tumors (judged by clinical imaging) will qualify. Inclusion Criteria Specific for Extracranial Neuroendocrine Tumors: - Histopathologically confirmed, well-differentiated metastatic neuroendocrine tumor. - ECOG performance status of 2 or better. - Patients receiving stable-dose somatostatin analogs (SSAs, long-acting release [LAR], depot) for >3 months before enrollment may be enrolled on the study, but such treatment is not required. Inclusion Criteria specific for Extracranial Primary Breast tumors: - Clinical and radiological diagnosis of a breast cancer - ECOG performance status of 2 or better. Inclusion Criteria specific for Rectal tumors: - Histologically confirmed colorectal cancer, which is located in the rectum. - ECOG performance status of 2 or better. Exclusion Criteria: - Patients who are pregnant or lactating are excluded. Exclusion Criteria Specific for Intracranial Tumors: - Severe increased intracranial pressure, status epilepticus, or other symptoms requiring emergency or urgent intervention. - Tumor surgery or radiation within 1 month prior to the PET scan Exclusion Criteria Specific for Extracranial Neuroendocrine Tumors: - Tumor-directed therapy within 3 months to the area of planned imaging. - Ongoing treatment with a targeted agent (e.g., sunitinib or everolimus) or receiving cytotoxic chemotherapy (e.g., capecitabine or temozolomide). - Use of telotristat ethyl (a tryptophan-hydroxylase inhibitor) within one month. Exclusion Criteria for Extracranial Primary Breast tumors: -Recent (within 1 month) tumor resection or radio-chemotherapy (acute/subacute post-treatment inflammatory changes may cause false positive increases on PET). Exclusion Criteria for Rectal tumors: -Active inflammatory bowel disease (Crohn's or Ulcerative colitis) involving the rectum.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Karmanos Cancer Institute

Address:
City: Detroit
Zip: 48201
Country: United States

Status: Recruiting

Contact:
Last name: Csaba Juhasz, MD, PhD

Phone: 313-966-5136
Email: csaba.juhasz@wayne.edu

Start date: September 29, 2022

Completion date: December 31, 2024

Lead sponsor:
Agency: Barbara Ann Karmanos Cancer Institute
Agency class: Other

Collaborator:
Agency: Washington University School of Medicine
Agency class: Other

Source: Barbara Ann Karmanos Cancer Institute

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05556473