Genomic Reassurance and Diagnostic Closure in Precision Oncology: A Preventable Hazard

Genomic findings can sharpen therapeutic decisions, but they can also provide false reassurance. In precision oncology, labels such as benign, nonactionable, or explanatory may be mistaken for evidence that symptoms or abnormal findings require no further evaluation. This Perspective argues that genotype-phenotype discordance should be treated as a safety signal. Simple report language, tumor-board checks, and artificial intelligence guardrails can preserve the value of genomics without allowing a molecular explanation to become diagnostic closure.

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Publication Details

Journal
Clinical Pharmacology & Therapeutics
Published
2026-11-08
DOI
https://doi.org/10.1002/cpt.70557
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Genomic Reassurance and Diagnostic Closure in Precision Oncology: A Preventable Hazard

Richard B. Kim, John D. Schuetz
2 links
Clinical Pharmacology & Therapeutics
Genomics and Rare Diseases
article

Genomic Reassurance and Diagnostic Closure in Precision Oncology: A Preventable Hazard

Richard B. Kim, John D. Schuetz
article en

Abstract

Genomic findings can sharpen therapeutic decisions, but they can also provide false reassurance. In precision oncology, labels such as benign, nonactionable, or explanatory may be mistaken for evidence that symptoms or abnormal findings require no further evaluation. This Perspective argues that genotype-phenotype discordance should be treated as a safety signal. Simple report language, tumor-board checks, and artificial intelligence guardrails can preserve the value of genomics without allowing a molecular explanation to become diagnostic closure.

Clinical Pharmacology & Therapeutics
Western University (CA), St. Jude Children's Research Hospital (US)
American Lebanese Syrian Associated Charities
Good health and well-being
Genomics and Rare Diseases
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