4.3 Editorial Material

Is It Time to Expand Our Definition of Clinical Utility?

Journal

CANCER CONTROL
Volume 30, Issue -, Pages -

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/10732748231170483

Keywords

cancer guidelines; genetic testing; circulating tumor Deoxyribonucleic acid; clinical utility; biomarker

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Currently, most patients are denied genetic tests for cancer risk or recurrence prediction due to the lack of proven clinical utility, although germline testing has been proven accurate and measures to prevent and diagnose early cancers associated with gene variations have been recommended. Similarly, despite the accuracy of ctDNA assays in predicting cancer recurrence, major organizations recommend against their use for monitoring solid tumor malignancies. This article discusses the reasons behind the lack of proven clinical utility and the need for a broader definition of clinical utility to benefit more patients.
Currently, genetic tests that predict cancer risk or risk of recurrence in patients who have had their cancer treated with curative intent must have proven clinical utility to be recommended by the organizations responsible for publishing the standard-ofcare guidelines for cancer care. Based on the current definition of clinical utility, most patients are denied testing for cancer-predisposing genes or pathogenic germline variants even though germline testing has been proven as highly accurate in identifying pathogenic germline variant carriers, there are measures recommended to prevent and diagnose early cancers associated with particular PGVs, and disparities in patient access to genetic tests are well described. Similarly, despite dozens of studies demonstrating that detected circulating tumor DNA (ctDNA) after curative intention therapy of different cancer types is a highly accurate biomarker that predicts recurrence, the major organizations that publish guidelines for cancer monitoring after curative intention therapy recommend against using ctDNA assays to detect minimal residual disease and thereby predict recurrence for all solid tumor malignancies. Here, the primary reasons that these genetic tests are considered to lack proven clinical utility and the primary evidence suggesting that a broader definition of clinical utility should be considered are discussed. By expanding the definition of clinical utility, many patients will benefit from the information gained from having these genetic tests.

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