- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04309422
Texture Features and PDL1 in CT-PET 18 FDG
Correlation Between Texture Features With CT-PET 18 FDG and Overexpression of PDL1 in Non-small-cell Lung Carcinomas During the Initial Staging.
Search correlation between texture features in CT-PET 18 FDG and overexpression of PDL1 in non-small cell lung carcinomas during the inital staging.
The hypothesis is that overexpression of PDL1is correlated with at least one texture feature among those selected.
84 CT-PET 18 FDG at the initial staging of a non small cell lung carcinoma (adenocarcinoma or squamous cell carcinoma), whose the biopsed site was the primitive site or the drainage lymphadenopathy, without previous treatment, were recruited and analyzed by a software allowing to estimate texture features.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Montpellier, France, 34295
- Uh Montpellier
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion criteria:
- adult patient ;
- first CT-PET 18 FDG realized for the inital staging ;
- absence of previous treatment for a thoracic neoplasm ;
- biopsy realized on the primitive site or local drainage lymphadenopathy ;
- primitive site viewable with morphological imagery ;
- availability of evaluation of PDL1's overexpression ;
Exclusion criteria
- Refusal to participate in this research
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Overexpression of PDL1
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Absence of overexpression of PDL1
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Correlation between at least one texture feature and overexpression of PDL1
Time Frame: 1 day
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Correlation between at least one texture feature and overexpression of PDL1
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1 day
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jean-Baptiste MALLET, University Hospitals of Montpellier
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
- RECHMPL19_0623
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
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