Prevalence of variant reclassification following hereditary cancer genetic testing

Jacqueline Mersch, Nichole Brown, Sara Pirzadeh-Miller, Erin Mundt, Hannah C. Cox, Krystal Brown, Melissa Aston, Lisa Esterling, Susan Manley, Theodora Ross

Research output: Contribution to journalArticlepeer-review

127 Scopus citations


IMPORTANCE Variant reclassification is an important component of hereditary cancer genetic testing; however, there are few published data quantifying the prevalence of reclassification. OBJECTIVE Retrospective cohort study of individuals who had genetic testing from 2006 through 2016 at a single commercial laboratory. DESIGN, SETTING, AND PARTICIPANTS A retrospective cohort of individuals who had genetic testing between 2006 and 2016 at a single commercial laboratory was assessed. Variants were classified as benign, likely benign, variant of uncertain significance, likely pathogenic, or pathogenic. Retrospective chart reviews were conducted for patients from the University of Texas Southwestern (UTSW) Medical Center. EXPOSURES Hereditary cancer genetic testing. MAIN OUTCOMES AND MEASURES Frequency of and time to amended reports; frequency and types of variant reclassification. RESULTS From 2006 through 2018, 1.45 million individuals (median [interquartile range] age at testing, 49 years [40.69-58.31 years], 95.6% women) had genetic testing, and 56.6% (n = 821 724) had a personal history of cancer. A total of 1.67 million initial tests were reported and 59 955 amended reports were issued due to variant reclassification. Overall, 6.4% (2868 of 44 777) of unique variants were reclassified. Reclassification to a different clinical category was rare among unique variants initially classified as pathogenic or likely pathogenic (0.7%, 61 of 9112) or benign or likely benign (0.2%, 15 of 8995). However, 7.7% (2048 of 26 670) of unique variants of uncertain significance were reclassified: 91.2% (1867 of 2048) were downgraded to benign or likely benign (median time to amended report, 1.17 years), 8.7% (178 of 2048) were upgraded to pathogenic or likely pathogenic variants (median time to amended report, 1.86 years). Because most variants were observed in more than 1 individual, 24.9% (46 890 of 184 327) of all reported variants of uncertain significance were reclassified. CONCLUSIONS AND RELEVANCE Following hereditary cancer genetic testing at a single commercial laboratory, 24.9% of variants of uncertain significance were reclassified, which included both downgrades and upgrades. Further research is needed to assess generalizability of the findings for other laboratories, as well as the clinical consequences of the reclassification as a component of a genetic testing program.

Original languageEnglish (US)
Pages (from-to)1266-1274
Number of pages9
JournalJAMA - Journal of the American Medical Association
Issue number12
StatePublished - Sep 25 2018

ASJC Scopus subject areas

  • Medicine(all)


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