Opinion|Videos|March 4, 2024
Determining Transarterial Chemoembolization (TACE) Candidacy for Patients with HCC
Michael Morse, MD, establishes his criteria for implementing TACE versus systemic therapy in HCC treatment.
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Pelareorep plus a checkpoint inhibitor earned FDA fast track designation for pretreated, inoperable, recurrent, or metastatic squamous cell anal carcinoma.
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The FDA approved gedatolisib in PIK3CA wild-type breast cancer, granted full approval to selpercatinib in RET fusion+ tumors, and more.
Iza-bren was approved in China for recurrent or metastatic ESCC following progression on platinum-based chemotherapy and PD-1/PD-L1 inhibition.
The TRIPP-FFX trial met its primary end points of local disease control and safety with P-32 microparticles plus FOLFIRINOX pancreatic adenocarcinoma.
Dostarlimab monotherapy met the primary end point of sustained clinical complete response at 12 months in the phase 2 AZUR-1 trial.
The decision does not reflect new concerns about the clinical efficacy or safety data from the phase 3 CARES-310 trial.
In case you missed any, check out our recap of the episodes of OncLive On Air that aired in June 2026.
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