Ireland
--:--IST
Latest
Clinical Trials in France / NCT06826066
Recruiting Not applicable

Involvement of the Immune System in Intrinsic Radiosensitivity

NCT06826066 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-05-12
Last updated
2026-01-15

Condition(s) studied

Neoplasms

Investigational drug(s) / intervention(s)

Blood samples

Blood samples: We propose to include patients who have been treated with radiotherapy and did not experience severe radiation-induced toxicity, after obtaining their informed consent. A blood sample will then be collected by the nursing staff from the Oncology-Radiotherapy department at Henri Mondor University Hospital. After the patient signs the consent form, each patient will have their clinical information recorded and a blood sample taken. The blood samples will be immediately transported, at room temperature, to the INSERM U955 i-Biot unit at Henri Mondor (serum, plasma, and PBMC). All samples will be frozen at -80°C for later analysis.

Study summary

Radiotherapy is one of the major treatments for cancer. It may be indicated in more than two-thirds of patients, regardless of cancer location or disease stage. The mechanisms of radiotherapy action are numerous: halting tumor proliferation, inducing tumor cell death, triggering anti-tumor immune responses, and ensuring both local and systemic tumor control. As a result, current treatments are highly effective, providing, for instance, a 5-year overall survival rate of about 90%-95% for localized breast and prostate cancers.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Patients who have been treated with radiotherapy * Absence of toxicity grade 2 or higher * Patients without psychiatric, sociological, family, or geographical difficulties that could interfere with patient compliance to the protocol or follow-up * Information and signed informed consent * Affiliated with social security Exclusion Criteria: * Inability to obtain patient consent * Patient refusing blood sample collection * Patient deprived of liberty or under legal protection (under guardianship, under curatorship) * Patients who have experienced radiation-induced toxicity of grade 2 or higher * Disease progression, relapse * Patient under State Medical Aid

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hôpital Henri Mondor, 1 rue Gustave Eiffel, Créteil Île-de-France Region Recruiting

More Assistance Publique - Hôpitaux de Paris trials in France

Other trials for the same condition

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 NCT06826066 on ClinicalTrials.gov ↗ ← All trials in France