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18F-FSPG PET/CT as a Non-Invasive Imaging Biomarker for Treatment Response to Chemoradiation in Esophageal Cancer

Reason given: \<75% participation

Key facts

Where
Houston, United StatesSee the site

Where in United States

  • M D Anderson Cancer CenterHouston, United StatesNo longer taking part

Trial details

Who runs it
M.D. Anderson Cancer Center
Trial code
NCT06549413
Record updated
13 August 2026
Original description
This study is being done to learn how 18F-FSPG PET/CT scan results may be related to the response to chemotherapy and radiation in patients with esophageal cancer.Read full original descriptionShow less

This study is being done to learn how 18F-FSPG PET/CT scan results may be related to the response to chemotherapy and radiation in patients with esophageal cancer.

Inclusion: * ≥ 18 years of age; Patients with locally advanced esophageal cancer; Patients with untreated documented carcinoma of the esophagus that is > 2 cm who are going to receive systemic therapy concurrently with radiation as primary therapy; Ability to provide written informed consent in accordance with institutional policies; Female subjects of childbearing potential must have a negative serum or urine pregnancy test within 1 week of the proposed investigational PET/CT scan(s) prior to injection of the investigational radiopharmaceutical.

Exclusion: * Body weight ≥ 400 pounds or body habitus or disability that will not permit the imaging protocol to be performed; Pregnant or lactating females; Have an allergy to intravenous contrast; eGFR < 30.

ClinicalTrials.gov NCT06549413

Under construction, not live – 18F-FSPG PET/CT as a Non-Invasive Imaging Biomarker for Treatment Response to Chemoradiation in Esophageal Cancer (NCT06549413) – Frontlight Research