Beyond traditional biopsy: integrating liquid biopsy, molecular panels, and advanced imaging techniques in thyroid cancer management.

Abdulkadir Eren, Emrah Karatay
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Abstract

The incidence of thyroid cancer has increased dramatically over the past four decades, making it the most common endocrine malignancy worldwide. Although well-differentiated thyroid carcinomas generally exhibit excellent survival rates following standard surgical and radioactive iodine interventions, the clinical management of high-risk variants, recurrent disease, and indeterminate nodules remains a significant challenge. Historically, the evaluation of thyroid nodules has relied on B-mode ultrasonography and fine-needle aspiration biopsy (FNAB). However, spatial and temporal tumor heterogeneity, coupled with the high rate of indeterminate cytology (Bethesda Categories III and IV), often leads to unnecessary diagnostic thyroidectomies. In recent years, liquid biopsy has emerged as a promising diagnostic approach, offering a non-invasive, dynamic, and comprehensive method for disease monitoring. This comprehensive review evaluates the biological mechanisms and clinical utility of circulating tumor DNA (ctDNA), circulating tumor cells (CTCs), extracellular vesicles (EVs), and non-coding RNAs in thyroid oncology. Furthermore, it explores the clinical role of commercial molecular diagnostic panels (e.g., Afirma GSC, ThyroSeq v3) in guiding surgical decisions. This review highlights the diagnostic synergy achieved when these molecular biomarkers are integrated with advanced radiological modalities - including strain elastography, quantitative region-of-interest (ROI) analysis, ACR TI-RADS, and cross-sectional volumetric tracking - as well as nuclear medicine techniques like technetium-99m MIBI scintigraphy. Emerging applications of artificial intelligence and radiomics in image analysis, alongside the concept of minimal residual disease monitoring, are also discussed. Ultimately, we emphasize the need for a multidisciplinary team (MDT) approach in translating these multi-omics and multimodal imaging data into precision medicine, while acknowledging current limitations and charting future directions.

超越传统活检:整合液体活检,分子面板和先进的甲状腺癌成像技术管理。
在过去的四十年中,甲状腺癌的发病率急剧增加,使其成为世界上最常见的内分泌恶性肿瘤。虽然高分化甲状腺癌通常在标准手术和放射性碘干预下表现出良好的生存率,但高风险变异、复发性疾病和不确定结节的临床管理仍然是一个重大挑战。历史上,甲状腺结节的评估依赖于b超和细针穿刺活检(FNAB)。然而,肿瘤的时空异质性,加上不确定细胞学(Bethesda分类III和IV)的高比例,往往导致不必要的诊断性甲状腺切除术。近年来,液体活检已成为一种很有前途的诊断方法,为疾病监测提供了一种非侵入性、动态和全面的方法。本文综述了循环肿瘤DNA (ctDNA)、循环肿瘤细胞(CTCs)、细胞外囊泡(ev)和非编码rna在甲状腺肿瘤中的生物学机制和临床应用。此外,它还探讨了商业化分子诊断面板(例如,Afirma GSC, ThyroSeq v3)在指导手术决策中的临床作用。这篇综述强调了当这些分子生物标志物与先进的放射学模式(包括应变弹性成像、定量感兴趣区域(ROI)分析、ACR TI-RADS和截面体积跟踪)以及核医学技术(如锝-99m MIBI显像)相结合时,所取得的诊断协同作用。人工智能和放射组学在图像分析中的新兴应用,以及最小残留疾病监测的概念,也进行了讨论。最后,我们强调需要多学科团队(MDT)方法将这些多组学和多模态成像数据转化为精确医学,同时承认当前的局限性并绘制未来的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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