Genomic Study for Families with Discordant Cancers

Genomic Analysis of Families With a History of Discordant Cancers

Recruiting Observational Study
Discordant Cancers
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 100
Sex
Any
Study type
Observational
Participants needed
150 (estimated)
Sponsor
Case Comprehensive Cancer Center · Other
Who this trial is looking for

This trial is looking for adults who have a family history of different types of cancer or who have been diagnosed with cancer themselves. Participants will provide a blood sample for genetic testing to help researchers understand the genetic links to cancer.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have a family history of cancer.
  • I have been diagnosed with cancer.
  • I have a family history of 5 or more different cancers.
  • I can provide a blood sample for testing.
  • I can receive genetic counseling.
  • I have at least one affected and one unaffected family member who can take part.

You may not be able to join if

  • I cannot safely provide a blood sample.
  • I cannot receive genetic counseling.
  • My family has a known high-risk cancer gene.
  • My family is not suitable for genetic evaluation.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial
The purpose of this study is to identify novel gene mutations which have contributed to significant personal and family history of cancer. Adults with and without cancer will be accrued to the study. Participants qualify to take part in this research study because someone in their family has been diagnosed with or because they themselves have a cancer diagnosis. Participants' DNA and other clinic…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Affected patient with a family history suggestive of a known hereditary syndrome or meeting NCCN criteria for germline testing and consent to a multicancer panel --This cohort is meant as a real world control group receiving routine standard of care and is not eligible for …
Contacts

Anna Mitchell, MD PhD

1-800-641-2422

CTUReferral@UHhospitals.org

CONTACT