“…Despite the lack of sound clinical evidence, there is sufficient pathophysiological rationale to use MKIs, particularly lenvatinib alone or in combination, for specific combinations of MPMNs, including DTC and most common associated SPCs 48,49,59 . Furthermore, there might be an even greater potential benefit of combining an MKI and a TKI for treatment of advanced malignancies (including DTC) according to therapeutic molecular targets based on common driver gene alterations and/or activated (initial or escape) signaling pathways 24,32–35,44,45,59,60 . For example, lenvatinib has shown promise in the simultaneous management of metastatic RR‐DTC and associated bowel malignancies in a patient with familial adenomatous polyposis 53 .…”