Benefit of Spectral Information in Patients Suspected for Lung Cancer
Recruiting
N/AInterventional Study
Lung Neoplasm Malignant
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
1,000 (estimated)
Sponsor
Copenhagen University Hospital at Herlev · Other
Who this trial is looking for
This trial is looking for patients who are suspected of having lung cancer. Participants will undergo different imaging tests to see how well they detect cancer and any additional steps needed based on the results.
Are You a Good Fit for This Trial?
You may be able to join if
I am suspected of having lung cancer
I have been referred to Copenhagen University Hospital
I can give informed consent
You may not be able to join if
I cannot tolerate intravenous iodinated contrast
I already have verified lung cancer from another institution
I have other health issues that prevent me from receiving treatment
I do not have a necessary reference standard like a biopsy or follow-up
I have known cancer outside of the lungs
There are technical limitations in my scans
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Purpose The aim of the study is to investigate the utilization of photon counting CT (PCCT) and the spectral information provided to determine the impact of spectral information on follow-up examinations.
As secondary aims we will compare conventional CT, CT + 18Flouro-deoxy-glucose (18F-FDG) positron emission tomography (PET) and PCCT + 18F-FDG PET for the tumor-node-metastasis (TNM) staging of …
Purpose The aim of the study is to investigate the utilization of photon counting CT (PCCT) and the spectral information provided to determine the impact of spectral information on follow-up examinations.
As secondary aims we will compare conventional CT, CT + 18Flouro-deoxy-glucose (18F-FDG) positron emission tomography (PET) and PCCT + 18F-FDG PET for the tumor-node-metastasis (TNM) staging of lung cancer patients.
PCCT with and without spectral information to assess the need for additional work-up,TNM classification, and sensitivity/specificity for malignant lesions. Patients will be randomized for reading with or without spectral information available within a clinical setting. The clinical readings are performed as a structured reports of all significant findings. Including both malignant and benign findings. Furthermore, in case additional follow-up/work-up is needed based on the guidelines on incidental findings by the American College of Radiology (ACR), this will be reported as well. If lesions suspicious of pulmonary malignancy is present, a provisional TNM classification is provided based on the scan findings.
After 3 months, the patient record is reviewed where additional examinations that can be attributed to the PCCT scan are recorded. The financial impact is calculated by a health economist based on the findings. PET/CT, conventional CT and PCCT combined with PET will be assessed retrospectively for comparison. Endpoints are number of supplementary examinations and cost savings. Sensitivity and specificity for any malignant finding. The T, N and M stages are assessed separately as diagnostic measures by the McNemar's test with a reference standard from the Danish Lung cancer register. The number of malignant lesions will be determined by reviewing the patient records incl. pathology assessment if available 12 months after inclusion of the last patient.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients suspected of lung cancer refered to Copenhagen University Hospital as per the guidelines from the danish national health authorities from either the general practitioner or from the department of pulmonology.
* Informed consent
Exclusion Criteria:
* Patients who can…
Inclusion Criteria:
* Patients suspected of lung cancer refered to Copenhagen University Hospital as per the guidelines from the danish national health authorities from either the general practitioner or from the department of pulmonology.
* Informed consent
Exclusion Criteria:
* Patients who cannot tolerate intravenous iodinated contrast
* Already verified lung cancer from another institution
* Comorbidities that exclude the patient from receiving treatment
* Lack of reference standard in the form of either histology or follow-up
* Known extrapulmonary malignancy
* Technical limitations within the scans/reconstructions
* other
Pr. the 29th of September included 433 participants.
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