- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07528131
18F-FDG PET/CT in Gastric Cancer (StomachCancer)
Role of 18F-FDG in Gastric Cancer
Study Overview
Status
Conditions
Detailed Description
This retrospective and prospective study was conducted to evaluate the effectiveness of 18 F-FDG PET/CT imaging in diagnosis of gastric cancer in correlation to other imaging modalities and clinical follow up.
This study included 50 patient pathologically proved gastric cancer. After obtaining written consent from the participants, detailed history was obtained from participants with the help of their data sheets, revision of pathology report (confirmed diagnosis of primary GC), the referral report from the treating physician and any imaging modalities patients were done, FDG PET/CT study was done using dedicated PET/CT scanner, and PET analysis was performed qualitatively and semi qualitatively, tissue biopsy was obtained from patients whenever it was possible.
Results of the current study demonstrate that FDG PET/CT was more accurate and more sensitive than CT in detection of occult distant metastases in advanced or equivocal cases, detection of metabolically active LNs that are morphologically normal on CT, helpful for recurrence detection, and informative for early metabolic response in FDG-avid tumors using standardized criteria (PERCIST),that may not be apparent using other modalities, and may have prognostic value that can change patient management.
PET/CT was more accurate than CT in Detection of Distant metastasis of gastric cancer (liver metastasis, lung metastasis, bone metastasis).
¹⁸F-FDG PET/CT is not a stand-alone staging tool for gastric cancer, but used selectively it meaningfully improves detection of distant metastasis, refines patient selection for radical treatment, and reduces futile surgery.
Clinicians must interpret PET/CT results in light of histologic subtype and complementary diagnostic procedures (endoscopy, laparoscopy, CT). Future work should validate FAPI tracers and define precise clinical pathways where PET/CT adds cost-effective benefit.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Sohag, Egypt, 82524
- Sara Saber Ahmed
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients diagnosed as Gastric Cancer on surgically resected specimens.
- Patients with gastric and extragastric metastasis.
- Patients with gastric cancer either operated or not
Exclusion Criteria:
- Patients with second malignancy (Double primary).
- Patient without proven pathology of Cancer Stomach.
- Severely ill patient (patient with disturbed conscious level, or couldn't lay supine during the imaging).
- Uncontrolled diabetic patient with blood glucose level more than 200mg\dl.
- Pregnant women.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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diagnosis ,staging ,assessment of treatment response and assessment of recurrence
Time Frame: 12months
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assess the value of SUVmax in every detected lesion in relation to the liver uptake and compare if this lesion deteced in other investigation
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12months
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- stomach cancer
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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