Open AccessAcquired Secondary RAS Mutation in BRAFV600E-Mutated Thyroid Cancer Patients Treated with BRAF Inhibitors
Author(s) -
Maria E. Cabanillas,
Ramona Dadu,
Priyanka Iyer,
Kacey Byrne Wanland,
Naifa L. Busaidy,
Anita K. Ying,
Maria Gule-Monroe,
Jennifer R. Wang,
Mark Zafereo,
MarieClaude Hofmann
Publication year - 2020
Publication title -
thyroid
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.918
H-Index - 142
eISSN - 1557-9077
pISSN - 1050-7256
DOI - 10.1089/thy.2019.0514
Subject(s) - dabrafenib , trametinib , medicine , thyroid cancer , anaplastic thyroid cancer , cancer research , vemurafenib , papillary thyroid cancer , mutation , v600e , cancer , melanoma , mek inhibitor , neuroblastoma ras viral oncogene homolog , oncology , kras , biology , gene , metastatic melanoma , mapk/erk pathway , colorectal cancer , genetics , kinase
Background: The BRAF V600E mutation is the most common driver mutation in papillary thyroid cancer (PTC) and anaplastic thyroid cancer (ATC). This mutation is considered actionable and, for BRAF V600E -mutated ATC, a BRAF inhibitor (dabrafenib) in combination with an MEK inhibitor (trametinib) is FDA approved. BRAF inhibitors have also shown efficacy in BRAF V600E -mutated PTC. However, as with all targeted therapies, resistance to these drugs eventually develops. It is essential that we understand the mechanisms of resistance to the BRAF inhibitors in thyroid cancer to develop future strategies to effectively treat these patients and improve survival. Patients: Herein, we describe four patients with thyroid cancer treated with selective BRAF inhibitors, who developed a RAS mutation in addition to the BRAF V600E mutation at progression. Results: Patients 1 and 3 acquired a KRAS G12V mutation in the progressive tumor, patient 2 acquired a NRAS Q61K mutation in a progressive lymph node, and patient 4 acquired NRAS G13D mutation on liquid biopsy performed at the time of radiographic disease progression. Conclusion: Similar to the melanoma experience, the emergence of RAS mutations appears to act as a mechanism of resistance to BRAF inhibitors in thyroid cancers.