Clinical genetic testing outcome with multi-gene panel in Asian patients with multiple primary cancers.

Pathogenic variants were found more frequently in younger patients, in those with a family history of cancer related to the suspected syndrome, and a trend towards significance in those with multiple primary cancers (35.5% vs. 25.6%, p = 0.09).

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Patients with multiple primary cancers were more likely to undergo testing than patients with 1 primary cancer (47.6% vs 41.0%, p=0.07), although the difference did not reach statistical significance.

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