Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT05214820

68Ga-PSMA PET Imaging of Upper Metastatic Gastric Cancers to Determine Eligibility to Endoradiotherapy

Led by Centre de recherche du Centre hospitalier universitaire de Sherbrooke · Updated on 2025-02-20

20

Participants Needed

1

Research Sites

180 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Upper gastrointestinal (GI) cancers are a major health problem in Canada. At the metastatic stage, options are limited (usually chemotherapy, immunotherapy, personalized therapies under research protocols). These options are not applicable to all patients and may have significant toxicities. Endoradiotherapy (ERT) using a radioisotope coupled with a localization vector specifically targeting tumor cells to deliver a localized dose of radiation therapy is a promising avenue as it can treat disseminated neoplastic disease in a specific manner sparing healthy tissue with minimal side effects. The main goal of this study is to confirm that patients with upper GI cancer would be eligible for ERT (177Lu-PSMA treatment by using 68Ga-PSMA PET/CT assessment).

CONDITIONS

Official Title

68Ga-PSMA PET Imaging of Upper Metastatic Gastric Cancers to Determine Eligibility to Endoradiotherapy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years and older
  • Diagnosed with active adenocarcinoma of the esophagus, stomach, bile ducts, or pancreas confirmed by a CT scan within the last 8 weeks
  • At least one lesion identified as stable or progressive cancer on CT imaging
  • No local therapy (such as radiotherapy or ablation) applied to lesions between the CT scan and 68Ga-PSMA PET imaging
  • Able to give free and informed consent
  • Able to undergo 68Ga-PSMA PET imaging within 2 months of the qualifying CT scan
Not Eligible

You will not qualify if you...

  • Having another active cancer, except non-metastatic non-melanoma skin cancer or cancers in remission for at least 3 years
  • ECOG performance status greater than 3
  • Being pregnant
  • Unable to follow study rules

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CIUSSS de l'Estrie- CHUS Hospital

Sherbrooke, Quebec, Canada, J1H 5N4

Actively Recruiting

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Research Team

A

Amélie Tétu, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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