Reimagining the Therapeutic Approach for Anaplastic Thyroid Cancer: The Roadmap to a Cure.

IF 5.8 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Thyroid Pub Date : 2025-05-01 DOI:10.1089/thy.2025.0044
Maria E Cabanillas, Neal Akhave, Victoria Banuchi, Naifa Busaidy, Ramona Dadu, Renata Ferrarotto, Gary B Gunn, Sarah Hamidi, Marie-Claude Hofmann, S Mohsen Hosseini, Priyanka C Iyer, Stephen Y Lai, Anna Lee, Anastasios Maniakas, Matthew S Ning, Michael Spiotto, Jennifer R Wang, Michelle D Williams, Mark Zafereo
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Abstract

Background: Anaplastic thyroid cancer (ATC) is an aggressive cancer that leads to rapid death if left untreated. However, recent advances in ATC treatment have dramatically changed the prognosis in a select group of patients with BRAFV600E mutations. In these patients, BRAF/MEK inhibitors have been shown to dramatically and rapidly shrink tumors. Yet, these responses are short-lived unless additional treatment modalities are applied. In patients without a BRAFV600E mutation, the current available therapies are far less effective. Summary: In this article, we review the relevant literature and propose applying the "Total Therapy" approach used since the 1960s for another deadly but curable disease, acute lymphocytic leukemia, to ATC. We have adapted the concepts of Induction, Consolidation, and Maintenance, applying them to ATC. This regimen integrates the treatments we have found to be successful in ATC: combination systemic therapy using targeted therapy plus immunotherapy, surgery, radiation, and continuation of the systemic therapy for several years, thereby attempting to eradicate all residual ATC cells. Conclusions: There has been a renewed interest in understanding the genomics of ATC and treating these patients with urgency rather than just providing palliative care. This shift has led to significant improvements in the prognosis of ATC. With the right tools and a clear roadmap to guide us, we now aim to take on the challenge of curing these patients.

重新构想间变性甲状腺癌的治疗方法:治愈的路线图。
背景:间变性甲状腺癌(ATC)是一种侵袭性癌症,如果不及时治疗可导致快速死亡。然而,ATC治疗的最新进展极大地改变了一组BRAFV600E突变患者的预后。在这些患者中,BRAF/MEK抑制剂已被证明能显著而迅速地缩小肿瘤。然而,除非采用额外的治疗方式,否则这些反应是短暂的。对于没有BRAFV600E突变的患者,目前可用的治疗方法的效果要差得多。摘要:在本文中,我们回顾了相关文献,并建议将自20世纪60年代以来用于治疗另一种致命但可治愈的疾病——急性淋巴细胞白血病的“全面治疗”方法应用于ATC。我们调整了归纳、巩固和维护的概念,将它们应用于ATC。该方案整合了我们发现在ATC中成功的治疗方法:联合全身治疗,使用靶向治疗加免疫治疗、手术、放疗和持续数年的全身治疗,从而试图根除所有残留的ATC细胞。结论:人们对了解ATC基因组学和紧急治疗这些患者产生了新的兴趣,而不仅仅是提供姑息治疗。这一转变显著改善了ATC的预后。有了正确的工具和清晰的路线图指导,我们现在的目标是接受治愈这些患者的挑战。
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来源期刊
Thyroid
Thyroid 医学-内分泌学与代谢
CiteScore
12.30
自引率
6.10%
发文量
195
审稿时长
6 months
期刊介绍: This authoritative journal program, including the monthly flagship journal Thyroid, Clinical Thyroidology® (monthly), and VideoEndocrinology™ (quarterly), delivers in-depth coverage on topics from clinical application and primary care, to the latest advances in diagnostic imaging and surgical techniques and technologies, designed to optimize patient care and outcomes. Thyroid is the leading, peer-reviewed resource for original articles, patient-focused reports, and translational research on thyroid cancer and all thyroid related diseases. The Journal delivers the latest findings on topics from primary care to clinical application, and is the exclusive source for the authoritative and updated American Thyroid Association (ATA) Guidelines for Managing Thyroid Disease.
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