NgoFebhuwari 2023, i-Food and Drug Administration (FDA) yasheshisa ukugunyazwa kwe-tucatinib (Tukysa, Seagen Inc.) kanye ne-trastuzumab yokwelashwa kwe-RAS wild-type HER2-positive colorectal cancer osusabalele noma ongakwazi ukuphinda ulashwe.
Novemba 2022: Inhlanganisela ye-doxorubicin, i-vincristine, i-etoposide, i-prednisone, ne-cyclophosphamide ene-brentuximab vedotin (Adcetris, Seagen, Inc.) igunyazwe i-Food and Drug Administration ukuze isetshenziswe ezinganeni.