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Clinical Trials/NCT03739281
NCT03739281
Terminated
Not Applicable

Advancing Diagnosis and Treatment for Lung Cancer Patients Using Hybrid PET/MR Imaging and Novel Visualization Tools

University Hospital of North Norway1 site in 1 country35 target enrollmentDecember 12, 2018
ConditionsLung Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lung Cancer
Sponsor
University Hospital of North Norway
Enrollment
35
Locations
1
Primary Endpoint
Sensitivity and specificity of PET/MR vs. clinical routine PET/CT
Status
Terminated
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this project is to investigate if PET/MR imaging improves the accuracy in visualization and characterization of lung cancer disease, compared to PET/CT.

Detailed Description

Lung cancer is the most frequent cancer type and the leading cause of cancer-related death worldwide. Positron emission tomography (PET) coupled with computed tomography (CT) is the standard of care for visualization and staging of lung cancer. Recent clinical introduction of hybrid PET and magnetic resonance (MR) imaging systems has shown potential to improve tumor imaging beyond the limits of PET/CT. However, knowledge about the clinical impact of this new hybrid modality is still limited. This project aims to investigate how PET/MR may improve the diagnosis and treatment of lung cancer disease, compared to PET/CT: PET/MR may allow early detection of brain and liver metastases, which strongly affects treatment outcome and survival; predictive models based on machine learning may combine image derived biomarkers from PET/MR, histology and health record data, to automatically visualize and characterize the tumor, facilitating computer aided diagnosis and personalized radiotherapy treatment.

Registry
clinicaltrials.gov
Start Date
December 12, 2018
End Date
December 31, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital of North Norway
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Referred to clinical PET/CT examination for investigation of lung disease.

Exclusion Criteria

  • Blood glucose level \>8.3 mmol/l
  • MR incompatible objects, e.g. metal implants, inside the body
  • Intolerance to gadolinium-based contrast agents, e.g. severe renal disease (GFR\<30).
  • Unable to give written consent.

Outcomes

Primary Outcomes

Sensitivity and specificity of PET/MR vs. clinical routine PET/CT

Time Frame: 1-2 weeks after the initial inclusion.

Sensitivity and specificity of PET/MR scans will be compared with in clinical routine PET/CT examinations for lung cancer disease feature prediction.

Secondary Outcomes

  • Prediction of treatment response and progression-free survival(5 years after inclusion.)

Study Sites (1)

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