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Except for targeting mutant IDHs, metabolic inhibitors are potentially active regardless of tumor genetic subtype and thus beneficial to the large majority of men with CRPC who are not currently candidates for precision medicine (e.g., DNA repair defects for PARP inhibitors or CDK12 loss for immunotherapy) (138, 163)

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Novartis, Basel, Switzerland), a tyrosine kinase inhibitor targeting the BcrAbl protein, is a first-line treatment for Philadelphia chromosome-positive CML [7]