Health patterns linked to inherited EGFR gene changes
Part of Cancer, Lungs & breathing clinical trials.
This study looks at people who have a certain change in the EGFR gene that they were born with. Researchers want to understand what health issues are linked to this gene change, which may help guide care for others with the same condition.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are 18 years old or older.
- You have a specific change (called a pathogenic variant) in the EGFR gene that you were born with.
- You have French social security coverage (not including AME, which is state medical help for people without papers).
- You are not under legal guardianship or curatorship.
- You agree to allow the researchers to use your medical data for this study.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This study looks for inherited (family-passed) genetic changes that may raise the risk of lung cancer and related thoracic cancers. It may help people and families understand their genetic risk by collecting health information and sometimes specimens from patients and relatives.
This study looks at real-world treatment for non-small cell lung cancer with a specific genetic change (EGFR mutation). It might help researchers understand how different treatments work in daily practice.
This study looks at how EGFR-mutated lung cancer changes over time and tries to find markers that can predict how well you might respond to treatment. You will provide a tumor sample for genetic analysis.
This study uses a blood test to look for signs of lung cancer in people who have never smoked or smoked very little. It focuses on Asian and Latinx communities because certain gene changes are more common in these groups.
This study looks at inherited genetic changes in people with a type of lung cancer called lung adenocarcinoma. The goal is to find gene variants linked to the disease, which may help guide future treatment decisions.
This study looks at genetic changes linked to breast, ovarian, or digestive cancers. It may help doctors better understand inherited cancer risks.
Hear when a new Bronchopulmonary Cancers trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.