Initial Management of BRAF V600E-Variant Anaplastic Thyroid Cancer

Author:

Hamidi Sarah1,Dadu Ramona1,Zafereo Mark E.2,Ferrarotto Renata3,Wang Jennifer R.2,Maniakas Anastasios2,Gunn G. Brandon4,Lee Anna4,Spiotto Michael T.4,Iyer Priyanka C.1,Sousa Luana G.3,Akhave Neal S.3,Ahmed Salmaan5,Learned Kim O.5,Lu Charles3,Lai Stephen Y.24,Williams Michelle6,Hosseini S. Mohsen6,Busaidy Naifa L.1,Cabanillas Maria E.1

Affiliation:

1. Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer, Houston

2. Department of Head & Neck Surgery, The University of Texas MD Anderson Cancer, Houston

3. Department of Thoracic−Head & Neck Medical Oncology, The University of Texas MD Anderson Cancer, Houston

4. Department of Radiation Oncology, The University of Texas MD Anderson Cancer, Houston

5. Department of Neuroradiology, The University of Texas MD Anderson Cancer, Houston,

6. Department of Pathology, The University of Texas MD Anderson Cancer, Houston

Abstract

ImportanceBRAF/MEK inhibitors revolutionized the treatment of BRAF V600E-variant anaplastic thyroid carcinoma (BRAFv-ATC), offering improved outcomes for patients with this previously incurable disease.ObservationsAnaplastic thyroid carcinoma (ATC) accounts for approximately half of thyroid cancer−related deaths. It presents as a rapidly growing tumor that often invades locoregional structures and spreads to distant sites early; therefore, prompt diagnosis, staging, and treatment initiation are of the essence in the treatment of ATC. Although most oncologists will encounter a patient with ATC in their practice, the rarity of this disease makes treatment challenging, particularly because those with BRAFv-ATC no longer have a dismal prognosis. BRAF/MEK kinase inhibitors have transformed the outlook and treatment of BRAFv-ATC. Therefore, molecular profiling to identify these patients is critical. More recently, the addition of immunotherapy to BRAF/MEK inhibitors as well as the use of the neoadjuvant approach were shown to further improve survival outcomes in BRAFv-ATC. Many of these recent advances have not yet been incorporated in the currently available guidelines, allowing for disparities in the treatment of patients with BRAFv-ATC across the US. With the increasing complexity in the management of BRAFv-ATC, this Consensus Statement aims to formulate guiding recommendations from a group of experts to facilitate therapeutic decision-making.Conclusions and RelevanceThis Consensus Statement from the FAST (Facilitating Anaplastic Thyroid Cancer Specialized Treatment) group at MD Anderson Cancer Center emphasizes that rapid identification of a BRAF V600E pathogenic variant and timely initiation of sequential therapy are critical to avoid excess morbidity and mortality in patients with BRAFv-ATC. In the past decade, remarkable progress has been made in the treatment of patients with BRAFv-ATC, justifying these new evidence-based recommendations reached through a consensus of experts from a high-volume center.

Publisher

American Medical Association (AMA)

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