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CompletedNCT03272997Updated Dec 17, 2020

The Value of PET-CT in Pleural Effusions

An observational study in Pleural Effusion, Malignant, sponsored by Naestved Hospital. Completed at 2 sites in Denmark. Open to participants aged 16 Years and older. Per ClinicalTrials.gov, last updated 2020-12-17.

Sponsored by Naestved Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
112
Ages
16 Years and older
Sex
All
01

Study 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 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).

02

Conditions studied

  • Pleural Effusion, Malignant

Keywords

  • Positron emission thomography
  • Computed tomography
  • Sensitivity
  • Specificity
03

Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Sampling method
Probability sample

Study population

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

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • Missing data
  • Lung cancer
  • Thoracic malignancies
04

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
112 participants (actual)
Patient registry
No
05

What researchers measure

Primary outcomes

  1. Sensitivity PET-CT

    TP / (TP + FN)

    Time frame: 1 year

Secondary outcomes

  1. CT-Specificity

    TN / (TN+FP)

    Time frame: 1 year

  2. PET-CT-Specificity

    TN / (TN+FP)

    Time frame: 1 year

  3. CT-Sensitivity

    TP / (TP + FN)

    Time frame: 1 year

  4. Comparison of the diagnostic power

    McNemars' test with Bonferroni

    Time frame: 1 year

  5. CT-Likelihood ratio+

    LR+ = sensitivity / (1-specificity)

    Time frame: 1 Year

  6. PET-CT-Likelihood ratio+

    LR+ = sensitivity / (1-specificity)

    Time frame: 1 Year

  7. CT-Likelihood ratio-

    LR- = (1-sensitivity) / specificity

    Time frame: 1 year

  8. PET-CT-Likelihood ratio-

    LR- = (1-sensitivity) / specificity

    Time frame: 1 year

  9. CT-positive predictive value

    PPV =TP / (TP+ FP)

    Time frame: 1 year

  10. PET-CT-positive predictive value

    PPV =TP / (TP+ FP)

    Time frame: 1 year

  11. CT-negative predictive value

    TN/ (TN + FN)

    Time frame: 1 year

  12. PET-CT-negative predictive value

    TN/ (TN + FN)

    Time frame: 1 year

  13. CT-Diagnostic accuracy

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

    Time frame: 1 year

  14. PET-CT-Diagnostic accuracy

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

    Time frame: 1 year

06

Study locations

2 sites
  • Naestved Hospital
    Naestved, 4700, Denmark
  • Naestved Hospital
    Næstved, 4700, Denmark
07

Registry details

Key details

Study ID
NCT03272997
Lead sponsor
Naestved Hospital
Responsible party
Simon Reuter (MD, Principal investigator, Naestved Hospital) — Principal investigator
First posted
Sep 6, 2017
Start date
Oct 1, 2017
Primary completion
Jan 31, 2018
Completion
Jan 30, 2019
Last update
Dec 17, 2020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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