Evidence map›Paper›PMID 35544645›Full record

ArticleJCO oncology practice2022

Disparities in Cancer Genetic Testing and Variants of Uncertain Significance in the Hispanic Population of South Texas.

Stephanie Soewito, Rachel Wyatt, Emily Berenson, Natalie Poullard, Shawn Gessay, Lindsey Mette, Elena Marin, Kristin Shelby, Elise Alvarez, Byeong Yeob Choi and 8 more

Abstract read
In one paragraph

Article in JCO oncology practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Stephanie SoewitoUniversity of the Incarnate Word, San Antonio, TX.
Rachel WyattDepartment of Pediatrics, UT Health San Antonio, San Antonio, TX.ORCID 0000-0002-1771-5358
Emily BerensonDepartment of Pediatrics, UT Health San Antonio, San Antonio, TX.
Natalie PoullardMays Cancer Center, UT Health San Antonio, San Antonio, TX.
Shawn GessayDepartment of Pediatrics, UT Health San Antonio, San Antonio, TX.
Lindsey MetteDepartment of Pediatrics, UT Health San Antonio, San Antonio, TX.
Elena MarinGreehey Children's Cancer Research Institute, UT Health San Antonio, TX.
Kristin ShelbyGreehey Children's Cancer Research Institute, UT Health San Antonio, TX.
Elise AlvarezMays Cancer Center, UT Health San Antonio, San Antonio, TX.
Byeong Yeob ChoiDepartment of Population Health Sciences, UT Health San Antonio TX, San Antonio, TX.ORCID 0000-0002-4205-1442
Clarissa AvilesGreehey Children's Cancer Research Institute, UT Health San Antonio, TX.
Anna Maria Pulido-SaldivarGreehey Children's Cancer Research Institute, UT Health San Antonio, TX.
Pamela M OttoDepartment of Radiology, UT Health San Antonio, San Antonio, TX.
Ismail JatoiMays Cancer Center, UT Health San Antonio, San Antonio, TX.ORCID 0000-0002-6775-0039
Chethan RamamurthyMays Cancer Center, UT Health San Antonio, San Antonio, TX.
Myron IgnatiusGreehey Children's Cancer Research Institute, UT Health San Antonio, TX.
Virginia G KaklamaniMays Cancer Center, UT Health San Antonio, San Antonio, TX.ORCID 0000-0002-3313-8458
Gail E TomlinsonDepartment of Pediatrics, UT Health San Antonio, San Antonio, TX.ORCID 0000-0003-2579-1833

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
NCI NIH HHS P30 CA054174
6 · The paper itself

Abstract

purposeRacial and ethnic disparities have included a lack of access to both genetic testing and research, resulting in poor understanding of the genomic architecture in under-represented populations. The South Texas population is primarily of Hispanic background and has been largely devoid of genetic services. We extended access to this underserved population and uncovered genetic variants previously not observed, emphasizing the need to continually improve both genomic databases and clarification of variant significance to provide meaningful patient counseling.

methodsThis study consisted of a retrospective cohort review of patients seen through a cancer genetics education and service program across 24 counties in South Texas. In total, 1,595 individuals were identified as appropriate for cancer genetic counseling and 1,377 completed genetic testing.

resultsEighty percent of those receiving genetic counseling self-identified as Hispanic, 16% as non-Hispanic White (NHW), 3% as African American, and 1% as other race/ethnicity. Of reported variants, 18.8% were pathogenic and 13.7% were reported as a variant of uncertain significance (VUS). VUS was reported in 17.2% of the Hispanic individuals compared with 9% NHW (

conclusionIndividuals of Hispanic ethnicity were significantly more likely to harbor a VUS compared with NHW. The extended reach into our regional communities revealed a gap in the ability to accurately interpret genomic variation with implications for advising patients on screening, prevention, and management strategies. A higher percentage of VUS also emphasizes the challenge of continued follow-up amid existing barriers that led to disparities in access. As understanding of the variants develops, hopefully gaps in knowledge of the genomic landscape will be lessened with increased clarity to provide accurate cancer risk assessment and recommendations for implementing prevention initiatives.

Indexed as

Hispanic or LatinoNeoplasmsGenetic TestingHumansRetrospective StudiesTexas

Identifiers

PMID35544645
PMCPMC10166383

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.