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Recruiting NCT06875700

Beliefs, Attitudes, and Response to Genetic Testing in SarcomaPatients

Observational Leiomyosarcoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Leiomyosarcoma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Beliefs, Attitudes, and Response to Genetic Testing in Sarcoma Patients

Overview

Genomic research has shown that a portion of leiomyosarcomas can be attributed to an underlying cancer predisposition syndrome. However, the optimal approach for incorporating germline testing into the care of these patients. This study is assessing the beliefs about the heritability of leiomyosarcoma and other cancer risks, and attitudes towards germline testing among leiomyosarcoma patients.

Detailed description

This is a descriptive study to explore attitudes to genomics and return of genetic information and examine the cognitive and affective impact of receiving germline genetic information among LMS patients and their family members.The present study will aim to do the following:

* Assess leiomyosarcoma (LMS) patients' beliefs and attitudes about the heritability of LMS and their interest in genetic testing. * Among LMS patients who undergo genetic testing, evaluate the cognitive, affective, and communication outcomes of genetic testing in LMS patients found to have actionable germline germline pathogenic variants (PVs). * Evaluate family members' beliefs and attitudes about the heritability of reasons for undergoing genetic testing and responses.

Prior studies of cancer patients have found a strong interest in genetic testing so at-risk relatives will have the opportunity to have increased cancer screening or take risk-reducing measures to prevent cancer. However, the genes most strongly associated with LMS are tumor protein 53 (TP53) gene and Retinoblastoma 1 (Rb1) gene. These genes cause risks for cancers that families may be less familiar with and that have less well-established approaches for screening and prevention.

LMS may not be the most significant cancer risk related to the syndrome associated with the PV identified. The finding of risk for other non-LMS cancers may be unexpected and incongruent with the family's experience or focus on the LMS being treated. Screening recommendations for relatives testing positive for these PV will generally be given cancer screening recommendations targeted towards risks for cancers other than LMS.

Patients beginning or in the midst of cancer treatment may be less able to share and effectively communicate about genetic test results to patients. We need to better understand how patients and family members respond to findings to maximize the clinical benefit of this information and support family communication.

LMS patients will be identified by querying the enterprise data warehouse (EDW) and Huntsman Tumor Registry and prospectively by reviewing clinic and tumor board lists.

Primary outcome measures

  • Beliefs about the heritability of Leiomyosarcoma [Time frame: up to 1 day from study enrollment]
Secondary outcome measures (1)
  • Interest in germline genetic testing [Time frame: up to 1 day from study enrollment]

Eligibility criteria

Inclusion LMS Proband

  • Actionable germline PV detected in the research context
  • Living
  • No prior germline testing for this PV
  • Able to speak and read English
  • Mentally competent
  • Age 18 or older

Relative of LMS Proband

  • 25-50% chance for having inherited the PV
  • No prior germline testing for this PV
  • Able to speak and read English
  • Mentally competent
  • Age 18 or older

Exclusion (both cohorts)

  • <18 years
  • Unable to read or write

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Family-based

Study locations

United States · 1 center
  • Huntsman Cancer Institute at the University of Utah — Salt Lake City

Identifiers

NCT: NCT06875700 · HCI165523 · 1P50CA272170-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗