Oncodrivers in Malignant Pleural Effusions Associated With Non-small Cell Lung Cancer: A Prospective Study.

Sponsor
Naestved Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04806412
Collaborator
(none)
100
1
25.9
3.9

Study Details

Study Description

Brief Summary

Oncological treatment of patients with disseminated non-small cell lung cancer (NSCLC) is depending on the status of programmed death-ligand 1 (PD-L1), anaplastic lymphoma kinase (ALK) and epidermal growth factor receptor (EGFR), so called oncodrivers. These can be measured in pleural fluid, but the prevalence is uncertain. In a prospective study, the research team aim to measure PD-L1, ALK and EGFR in patients with pleural fluid cytology positive for NSCLC to report the prevalence. Also, the study will investigate if the chance of obtaining oncodriver status is depending on the volume analysed and how the lack of oncodrivers influence the following work-up.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: meassurement of PD-L1, ALK, EGFR
N/A

Detailed Description

The study is a prospective, non-randomized, cohort study of patients with pleural effusion. Participants will be recruited from patients referred to the Pleura Clinic or admitted at the ward at the Department of Respiratory Medicine, Næstved Hospital, Næstved or at the Department of Respiratory Medicine, Zealand University Hospital, Roskilde, which is the two regional centres for workup of pleural effusions. Patients will be referred from either general practice or other hospital departments.

Pleural fluids with cytology positive for NSCLC will be tested for oncodrivers (for squamous cell carcinomas (SCC): PD-L1, for adenocarcinomas (AC): PD-L1, ALK and EGFR).

Follow-up will be 8 weeks after inclusion.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
prospective, non-randomized, cohort studyprospective, non-randomized, cohort study
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
The Prevalence of Oncodrivers in Malignant Pleural Effusions Associated With Non-small Cell Lung Cancer: A Prospective Study.
Actual Study Start Date :
Mar 15, 2021
Anticipated Primary Completion Date :
Mar 12, 2023
Anticipated Study Completion Date :
May 12, 2023

Outcome Measures

Primary Outcome Measures

  1. Prevalence of oncodriver status [assessed at 8 weeks follow-up]

    Prevalence of oncodriver status (for squamous cell carcinomas (SCC): PD-L1, for adenocarcinomas (AC): PD-L1, ALK and EGFR) in pleural fluid in patients with cytology positive for pulmonary NSCLC

Secondary Outcome Measures

  1. Proportion of adequate and inadequate pleural fluid specimens [assessed at 8-week follow-up]

  2. Amounts of pleural fluid sent for analysis [assessed at 8-week follow-up]

    Meassured in mL.

  3. Correlation between amounts of pleural fluid sent to the pathologist and the chance of obtaining oncodriver status [assessed at 8-week follow-up]

  4. Number and type of additional diagnostic interventions including additional thoracentesis and cytological or histological biopsies [assessed at 8-week follow-up]

  5. Prevalence of oncodriver status in additional diagnostic interventions [assessed at 8-week follow-up]

  6. - Correlation between oncodriver status obtained in pleural fluid specimens and cytological or histological biopsies [assessed at 8-week follow-up]

  7. - Proportion of work-ups where the lack of obtained oncodriver status in pleural fluid specimens leads to additional diagnostic interventions including additional thoracentesis and cytological or histological biopsies [assessed at 8-week follow-up]

  8. - Proportion of work-ups where full oncodriver-status was obtained at the second thoracentesis [assessed at 8-week follow-up]

  9. - Proportion of patients with pleural fluid cytology negative of NSCLC, who is diagnosed with NSCLC. [assessed at 8-week follow-up]

  10. Patient assessed pain during thoracentesis [at day 1, 2 minutes after thoracentesis]

    assessed by a questionnaire containing a VAS (Visual Analogue Scale, scale 0-10, 0 being no pain, 10 being the worse pain)

  11. Proportion of patients experiencing pneumothorax [assessed at day 1, 10 minutes after thoracentesis and 8-week follow-up by evaluating the patient file]

  12. Proportion of patients experiencing bleeding [assessed at day 1, 10 minutes after thoracentesis and 8-week follow-up]

  13. Proportion of complications leading to admission [assessed at 8-week follow-up]

    assessed by evaluating the patient file

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age ≥ 18 years

  • Pleural effusion known or suspected of association with NSCLC (pleural fluid cytology positive for cells from NSCLC)

  • Patients must be able to give informed consent

Exclusion Criteria:
  • Full oncodriver status measured in any pleural fluid in current work-up

  • Inability to understand written or spoken Danish.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Næstved Sygehus, department of pulmonary medicine Næstved Region Sjælland Denmark 4700

Sponsors and Collaborators

  • Naestved Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Naestved Hospital
ClinicalTrials.gov Identifier:
NCT04806412
Other Study ID Numbers:
  • SJ-889
First Posted:
Mar 19, 2021
Last Update Posted:
May 17, 2022
Last Verified:
May 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 17, 2022