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Recruiting Observational

Inflammation, Cachexia and Therapeutic Response in Lung Cancer Treated With Immune Checkpoint Inhibitors: Exploratory Observational Study

NCT07004868 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-06-03
Last updated
2025-08-11

Condition(s) studied

Lung Cancer (NSCLC)

Study summary

Lung cancer is the leading cause of cancer-related death in France and globally, with 2.48 million new cases diagnosed in 2022, accounting for nearly 13% of global cancer incidence. Despite recent advances, it remains a major health issue due to late-stage diagnosis and high patient and societal burden. New insights into tumor and immune pathways have led to the development of targeted therapies, including tyrosine kinase inhibitors and therapeutic antibodies. Among these, immune checkpoint inhibitors (ICIs) such as nivolumab, pembrolizumab, atezolizumab, and durvalumab have significantly improved outcomes for some patients by reactivating T-cell responses.

The LCAb (Lung Cancer Antibodies) research project focuses on studying the interindividual variability of clinical response to ICI in lung cancer. These therapies are now used across various lung cancer types and stages, including early and advanced disease. Most ICIs are administered at fixed doses, without considering patient-specific factors as blood concentrations, tumor burden, body weight or nutritional status. The study hypothesizes that fixed dosing may affect treatment response and survival outcomes, highlighting the need for more personalized approaches.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age greater than or equal to 18 years * Diagnosis of lung cancer, any histology, any stage * Treatment with Ab ICI, with or without chemotherapy * 1st administration of Ab ICI Exclusion Criteria: * Patient not followed at the CHRU de Tours * Person under protective supervision * Opposition to data processing

Primary outcome measure(s)

  • time to progression — Month 36
    time between 1st administration of Ab ICI and progression or death from any cause.

Trial sites (1)

FacilityCityRegionStatus
university hospital, Tours Tours France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07004868 on ClinicalTrials.gov ↗ ← All trials in France