Study rare solid tumors and collect your health samples
Part of Cancer clinical trials.
This study follows people (and sometimes family members) connected to rare solid tumors and collects health information and samples (biospecimens). It helps researchers understand how these cancers develop and builds resources for future research, which may benefit you by contributing to better tailored care for rare cancers.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You (or the person in your family) has a rare solid tumor, or a related genetic link
- If you have a rare tumor: it must be considered rare (fewer than 15 new cases per 100,000 people per year)
- If you don’t have the tumor: you must have a known inherited (germline) genetic change linked to rare solid tumors
- If you’re a family member: you must not already have a known inherited genetic change linked to rare solid tumors
- You must be able to understand the study and agree to sign consent
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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