The EHE observational study was developed to obtain a high number of datas such as clinical presentation, natural history, and treatment outcomes, cto identificate cytokines and hormones as biomarkers and generate patient-derived preclinical models as a tool to assess the activity of anticancer agents and validate novel therapeutic targets
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Demographic description
Timeframe: Through study completion, an average of 1 year
Patient status
Timeframe: Through study completion, an average of 1 year
Tumor-related symptoms
Timeframe: Through study completion, an average of 1 year
Tumor-related pain
Timeframe: Through study completion, an average of 1 year
Clinical prognosis
Timeframe: Through study completion, an average of 1 year
radiological features
Timeframe: Through study completion, an average of 1 year
correlation between radiological features and outcome
Timeframe: Through study completion, an average of 1 year
radiological response and systemic treatment
Timeframe: Through study completion, an average of 1 year