Genetic Investigation of Cancer Predisposition

This observational study, called "Genetic Investigation of Cancer Predisposition," aims to understand why some people develop cancer by looking for specific genetic changes. Researchers will collect clinical information and samples like blood, saliva, and tumor tissue from people with multiple cancers or a family history of cancer. They will use DNA or RNA sequencing to identify rare genetic changes that might be linked to cancer. The study will also look for these genetic changes in family members. The goal is to find rare genetic variants and tumor-specific mutations. This study is open to people of all ages who have a personal history of cancer before age 50, more than one primary cancer, or cancer with a family history that doesn't fit typical hereditary cancer patterns. The current status of this study is unclear.

Study design
This is an observational study that plans to enroll 100 participants. It is not a treatment study, but rather aims to understand genetic factors related to cancer.
What's involved
You would provide clinical information and samples such as blood, saliva, and tumor tissue. These samples will be used for genetic sequencing.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoints, such as identifying genetic variants, will be measured through study completion, which is approximately 6-12 months.

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NCT04620278

Genetic Investigation of Cancer Predisposition

Not Yet Recruiting
Not specifiedAll AgesObservational
The University of Texas Health Science Center at San Antonio
~100 participants
Updated 2026-01-06 on ClinicalTrials.gov
What's tested:DNA or RNA Sequencing

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Identification of Rare Genetic Variant
Measured over through study completion- approximately 6-12 months
+2 more outcomes measured
Genetic Predisposition
Cancer
1 sites across 1 states
Texas1
  • Patricia L Dahia, MD, PhD · PRINCIPAL_INVESTIGATOR · University of Texas Health at San Antonio

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  • Identification of Rare Genetic Variantthrough study completion- approximately 6-12 months

    Genetic screen detects a mutation that is likely responsible for tumor development

  • Identification of somatic (tumor only) mutationthrough study completion- approximately 6-12 months

    Genetic screen detects a mutation that is likely responsible for tumor development

  • Identification of Rare Genetic Variant in family membersthrough study completion- approximately 6-12 months

    Genetic screen detects a mutation that is likely responsible for tumor development