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Pleural Effusion, MalignantNCT03272997

The Value of PET-CT in Pleural Effusions

An observational study of Pleural Effusion, Malignant, run by Naestved Hospital at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The investigators aim is to asses the diagnostic power of 18F-FDG PET-CT in discriminating malignant from nonmalignant causes in patients with a recurrent unilateral pleural effusion of unknown origin. Read more about this study

Who is it for?
Ages 16 years and older
Conditions the study is for
Pleural Effusion, Malignant
How many people
112 participants
Where
1 siteDenmark
Study dates
1 Oct 2017to 30 Jan 2019
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 years and older
  • All sexes
  • Child, Adult, Older adult

Study population: All patients with a unilateral pleural effusion of unknown origin examined with the above

Who may be able to join

  • Thoracocentesis
  • Chest X-ray
  • CT scanning
  • PET-CT scanning

Who cannot join

  • Missing data
  • Lung cancer
  • Thoracic malignancies

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Naestved Hospital

    Næstved, 4700

Other trials in Denmark

About this study

Official title: The Diagnostic Power of 18F-FDG PET-CT Scanning for Discriminating Malignant From Non-malignant Causes in Unilateral Pleural Effusions

The investigators aim is to asses the diagnostic power of 18F-FDG PET-CT in discriminating malignant from nonmalignant causes in patients with a recurrent unilateral pleural effusion of unknown origin.

Read the detailed description

The investigators follow the STARD 2015 guideline for reporting diagnostic accuracy studies.

The investigators will review the hospital's administrative database of patients who underwent a thoracocentesis from January 2013 to January 2015. Patients at Department of Respiratory Medicine, Zealand University Hospital, Roskilde and Department of Respiratory Medicine, Naestved Hospital, Region Zealand, Denmark (two large respiratory centres with specialised functions) is eligible for inclusion. Patients are included irrespective of cytology and chemical analysis.

The investigators will review the patients' medical records and images retrospectively. To reduce the number of false negatives, the investigators complete a 1-year follow-up.

Patients older than 16 years are included, irrespective of smoking history and comorbidities, if both thoracocenteses, chest x-ray, a CT-scanning and a PET-CT scanning is performed. Exclusion criteria are previously diagnosed lung cancer, thoracic malignancy or incomplete data.

Classification of results The investigators chose the combination of investigations recommended by the internationally acknowledged BTS guideline, which is endorsed by the Danish Society of Respiratory Medicine. Thoracocentesis, chest x-ray, CT findings and PET-CT findings is categorized as either normal (i.e. not suggestive of any aetiology of the unilateral pleural effusion), suggestive of other lung pathology or suggestive of malignancy (i.e. representing a possible aetiology of the unilateral pleural effusion).

The thoracocentesis is classified as malignant if cytological examination revealed malignant cells. The chest x-ray is classified as malignant if suspicion of malignant disease is not rejected. The CT findings are classified as malignant according to Leung et. al. for pleural abnormalities (circumferential pleural thickening, nodular pleural thickening, parietal pleural thickening > 1 cm and mediastinal pleural involvement) and The Fleischner Society for parenchymal abnormalities (nodules > 8 mm). The PET-CT findings are classified as malignant if any findings suspicious for malignancy.

CT and PET-CT images, as well as the scan reports by the radiologist and the nuclear medicine physician, is reviewed by two experienced pulmonologists. They are blinded to all patient information, including final diagnosis.

The final diagnosis, the reference standard, is extracted from the patients' medical records. When no diagnosis is found, two investigators agree on a consensus diagnosis based on all investigation results. If no reasonable diagnosis can be established based on the findings, the patient case is categorized as having no final diagnosis. These cases are treated as a worst-case scenario, i.e. patients with a malignant disease are treated as false negative, and patients without malignant disease are treated as false positive.

Statistics Data are presented as frequencies and/or mean ± standard deviation (SD). Test characteristics were compared using McNemar's test with Bonferroni correction (two-sided level of significance < o.o5). Diagnostic power of thoracocentesis, chest x-ray, CT-scanning, PET-CT scanning and the combination are calculated. Diagnostic power is defined as true positive, true negative, false positive, false negative, sensitivity, specificity, likelihood ratio+, likelihood ratio-, positive predictive value (PPV), negative predictive value (NPV) and diagnostic accuracy (TP+TN)/(TP+FP+TN+FN).

The combined sensitivity will be calculated using the formula:

Sensitivitytest A + Sensitivitytest B + Sensitivitytest … - (Sensitivitytest A x Sensitivitytest B x Sensitivitytest …)

The combined specificity will be calculated using the formula:

Specificitytest A x Specificitytest B x Specificitytest… Data were analyzed using STATA (StataCorp LLC, Version 15.0, College Station, Texas, USA).

Keywords
Positron emission thomography, Computed tomography, Sensitivity, Specificity
Medical subject headings
Pleural Effusion, Malignant, Hypersensitivity

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Sensitivity PET-CT

    TP / (TP + FN)

    Measured: 1 year

Secondary outcomes (14)
  1. CT-Specificity

    TN / (TN+FP)

    Measured: 1 year

  2. PET-CT-Specificity

    TN / (TN+FP)

    Measured: 1 year

  3. CT-Sensitivity

    TP / (TP + FN)

    Measured: 1 year

  4. Comparison of the diagnostic power

    McNemars' test with Bonferroni

    Measured: 1 year

  5. CT-Likelihood ratio+

    LR+ = sensitivity / (1-specificity)

    Measured: 1 Year

  6. PET-CT-Likelihood ratio+

    LR+ = sensitivity / (1-specificity)

    Measured: 1 Year

  7. CT-Likelihood ratio-

    LR- = (1-sensitivity) / specificity

    Measured: 1 year

  8. PET-CT-Likelihood ratio-

    LR- = (1-sensitivity) / specificity

    Measured: 1 year

  9. CT-positive predictive value

    PPV =TP / (TP+ FP)

    Measured: 1 year

  10. PET-CT-positive predictive value

    PPV =TP / (TP+ FP)

    Measured: 1 year

  11. CT-negative predictive value

    TN/ (TN + FN)

    Measured: 1 year

  12. PET-CT-negative predictive value

    TN/ (TN + FN)

    Measured: 1 year

  13. CT-Diagnostic accuracy

    (TP+TN) / (TP+TN+FP+FN)

    Measured: 1 year

  14. PET-CT-Diagnostic accuracy

    (TP+TN) / (TP+TN+FP+FN)

    Measured: 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Sep 2017
  2. Study start1 Oct 2017
  3. Primary completion31 Jan 2018
  4. Study completion30 Jan 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
112 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03272997
Sponsor's protocol ID
PET-CT in UPE
Status last verified
Dec 2020
First submitted
30 Aug 2017
Last updated
17 Dec 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Pleural Effusion, Malignant, run by Naestved Hospital at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 17 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Sensitivity PET-CT (time frame: 1 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Dec 2020.

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