RecruitingNCT04807127

A Single-cell Approach to Identify Biomarkers of Pulmonary Toxicity for Immune Checkpoint Blockade


Sponsor

Universitaire Ziekenhuizen KU Leuven

Enrollment

60 participants

Start Date

Feb 1, 2020

Study Type

OBSERVATIONAL

Conditions

Summary

The main goal of this prospective non-interventional exploratory monocentric study is to characterize the immune cell composition of bronchoalveolar lavage (BAL) fluid from cancer patients experiencing cancer therapy-induced pneumonitis on a single-cell scale. These mechanistic insights can directly lead to putative diagnostic biomarkers and therapeutic targets. A second highly clinically relevant hypothesis is that single-cell profiling of blood samples will reveal circulating biomarkers of ICB toxicity, making non-invasive diagnosis feasible.


Eligibility

Min Age: 18 YearsMax Age: 120 Years

Inclusion Criteria5

  • Adult M/F/X (>= 18 years)
  • Patients receiving or having received treatment per guidelines
  • Patients undergoing bronchoscopy with BAL, for possible cancer treatment-induced pneumonitis
  • Not included in other clinical trials
  • Signed informed consent form

Exclusion Criteria1

  • Collected material not suitable for further processing in this study (e.g. bad quality). This decision will be made in consultation with a lab technician and/or bio-informatician, specialized in single-cell analysis.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGImmune checkpoint blockade

ICI, administered as standard-of-care treatment

DRUGTargeted therapy

TKI, administered as standard-of-care treatment

RADIATIONRadiotherapy

RT, administered as standard-of-care treatment


Locations(1)

Universitaire Ziekenhuizen Leuven

Leuven, Flemish Brabant, Belgium

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04807127


Related Trials