Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer, Houston.
Department of Head & Neck Surgery, The University of Texas MD Anderson Cancer, Houston.
JAMA Oncol. 2024 Sep 1;10(9):1264-1271. doi: 10.1001/jamaoncol.2024.2133.
BRAF/MEK inhibitors revolutionized the treatment of BRAF V600E-variant anaplastic thyroid carcinoma (BRAFv-ATC), offering improved outcomes for patients with this previously incurable disease.
Anaplastic 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.
This 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.
BRAF/MEK 抑制剂彻底改变了 BRAF V600E 变体间变性甲状腺癌(BRAFv-ATC)的治疗方法,为这种以前无法治愈的疾病患者带来了更好的治疗效果。
间变性甲状腺癌(ATC)约占甲状腺癌相关死亡人数的一半。它表现为一种快速生长的肿瘤,通常会早期侵犯局部和区域结构并扩散到远处;因此,及时诊断、分期和开始治疗对于 ATC 的治疗至关重要。尽管大多数肿瘤学家在其实践中都会遇到 ATC 患者,但这种疾病的罕见性使其治疗具有挑战性,尤其是因为那些患有 BRAFv-ATC 的患者的预后不再黯淡。BRAF/MEK 激酶抑制剂改变了 BRAFv-ATC 的前景和治疗方法。因此,识别这些患者的分子谱至关重要。最近,将免疫疗法添加到 BRAF/MEK 抑制剂中以及使用新辅助方法,进一步提高了 BRAFv-ATC 的生存结果。这些最近的进展中的许多尚未纳入当前可用的指南中,导致美国各地 BRAFv-ATC 患者的治疗存在差异。随着 BRAFv-ATC 管理的日益复杂化,本共识声明旨在制定一组专家的指导建议,以促进治疗决策。
MD 安德森癌症中心 FAST(促进间变性甲状腺癌专门治疗)小组的这份共识声明强调,快速识别 BRAF V600E 致病性变异体并及时开始序贯治疗对于避免 BRAFv-ATC 患者的过多发病率和死亡率至关重要。在过去十年中,BRAFv-ATC 患者的治疗取得了显著进展,这些新的基于证据的建议是由一个高容量中心的专家共识达成的,这是合理的。