INTRODUCTION: being the predominant driver in recurrent disease, for which effective and durable treatment options remain limited. AREAS COVERED: This article reviews the mechanistic rationale for combined RAF/MEK and focal adhesion kinase (FAK) inhibition in LGSOC, focusing on avutometinib (a first-in-class RAF/MEK clamp) and defactinib (a selective FAK inhibitor). A structured review of preclinical and clinical evidence was conducted, including key findings from phase I FRAME and phase II RAMP-201 trials. Efficacy outcomes, safety and tolerability profiles, and the current regulatory landscape, including accelerated approval in the United States and ongoing phase III evaluation, are discussed. EXPERT OPINION: -mutant tumors. If confirmed in phase III trials, this combination may establish a molecularly informed disease-specific treatment paradigm with the potential for more durable disease control than existing therapies.
Podder et al. (Thu,) studied this question.