- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06555861
Local Recurrence Prediction of by Texture Analysis Derived From Positron Emission Tomography (PET / CT) Imaging of Non-small Cell Lung Cancer (NSCLC) Treated With Stereotactic Radiotherapy (SBRT) (Retros MUMOFRAT) (MUMOFRAT retro)
August 13, 2024 updated by: University Hospital, Brest
Local Recurrence Prediction of by Texture Analysis Derived From Positron Emission Tomography (PET / CT) Imaging of Non-small Cell Lung Cancer (NSCLC) Treated With Stereotactic Radiotherapy (SBRT)
The aim of this retrospective multicentric study was to develop and evaluate a prognostic FDG PET/CT radiomics signature in early-stage non-small cell lung cancer (NSCLC) patients treated with stereotactic radiotherapy (SBRT).
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Actual)
87
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Brest, France, 29609
- CHRU de Brest
-
Rennes, France, 35042
- Centre Eugènes Marquis
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Tours, France, 37000
- CHU de Tours
-
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Saint Herblain
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Nantes, Saint Herblain, France, 44800
- ICO
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Eighty-seven patients with NSCLC stage I-II and tumours diameters below 5 cm according to the 8th American Joint Committee on Cancer classification, treated with definitive curative SBRT from January 2012 to December 2016 at 4 French institutions (Rennes, Tours, Brest and Nantes) were retrospectively included.
Description
Inclusion Criteria:
- NSCLC stage I-II treated by SBRT
- PET/CT imaging performed within 60 days of SBRT
Exclusion Criteria:
- Lack of follow-up
- Refusal of consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Local Recurrence
Time Frame: Time-to-Event measures up to 5 years
|
accuracy
|
Time-to-Event measures up to 5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cancer specific survival
Time Frame: Time-to-Event measures up to 5 years
|
accuracy
|
Time-to-Event measures up to 5 years
|
|
Distant metastasis free survival
Time Frame: Time-to-Event measures up to 5 years
|
accuracy
|
Time-to-Event measures up to 5 years
|
|
Recurrence free survival
Time Frame: Time-to-Event measures up to 5 years
|
accuracy
|
Time-to-Event measures up to 5 years
|
|
Overall survival
Time Frame: Time-to-Event measures up to 5 years
|
accuracy
|
Time-to-Event measures up to 5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 7, 2019
Primary Completion (Actual)
February 6, 2019
Study Completion (Actual)
February 6, 2019
Study Registration Dates
First Submitted
August 13, 2024
First Submitted That Met QC Criteria
August 13, 2024
First Posted (Actual)
August 15, 2024
Study Record Updates
Last Update Posted (Actual)
August 15, 2024
Last Update Submitted That Met QC Criteria
August 13, 2024
Last Verified
December 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 29BRC18.0283 - Retros MUMOFRAT
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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