Skip to main content
OpenTrials
Recruiting

NCT Number: NCT04886401

Retrospective Observational Study on Prediction of Response to PD-1 Immunotherapy in Patients with NSCLC

Therapeutic antibodies that block the programmed death-ligand 1 (PD-L1)/programmed death-1 (PD-1) pathway have revolutionized immuno-oncology by inducing robust and durable responses in patients with various cancer including advanced non-small-cell lung cancer (NSCLC). However, these responses only occur in a subset of patients, even in case of PD-L1 overexpression. Elucidating the determinants of response and resistance but also of severe immune-mediated adverse events is key to improving outcomes and developing new treatment strategies. Biomarkers that predict immune checkpoint inhibitors efficacy and toxicity are urgently needed and could emerge from characterization of tumor microenvironment.

The purpose of PREDICTION project is to elucidate response and toxicity predictive immunophenotypic signatures using a new in situ multiplexed strategy with imaging mass cytometry Hyperion. Patients treated with anti-PD-1 pembrolizumab will be selected on their response and toxicity profiles. Then, tumor samples will be analysed with Hyperion technology, allowing delineation of cell subpopulations and cell-cell interactions, highlighting tumor heterogeneity and to determine correlations between response and toxicity features. The number of co-analysable markers enables global vision on the same tissue section. A better understanding of the tumor microenvironment complex system will lead to discover new predictive biomarkers potentially transferable to current practice.

Recruiting

Interested in participating?

Request Info

Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU de Brest

Brest, 29609, France

Location status: Recruiting

Location contact

Margaux GEIER

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients
  • Advanced NSCLC with PD-L1 TPS of 50% or greater
  • Administration of first line pembrolizumab between January 2017 & December 2019

Exclusion criteria

  • Auto-immune disease
  • Prior exposure to immunotherapy
  • First dose pembrolizumab administered after December 2019

Treatment and study plan

Primary outcomes

  1. Identifying predictive biomarkers of anti-PD-1 response

    Time frame: 1 year

    Identifying predictive biomarkers of anti-PD-1 response by highlighting discriminant cell profiles between responder and non-responder patients

Study contacts

Contact information is provided by the study sponsor or research team.

Margaux GEIER, MD

CONTACT

[email protected]

02 30 33 80 30

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Official study title

Retrospective Observational Study on Prediction of Response to PD-1 Immunotherapy in Patients with Non Small Cell Lung Cancer Mass Tissue Imaging HyperIONTM

Acronym: PREDICTION

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
May 14, 2021
Registry last updated
Feb 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.