肝细胞癌治疗后疗效评价

A. Choudhari, S. Kulkarni, N. Shetty, K. Gala, Daksh Chandra, A. Baheti
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引用次数: 1

摘要

肝细胞癌(HCC)是世界范围内发病率和死亡率的主要原因,包括在印度。由于生活方式疾病,如肥胖、糖尿病、非酒精性脂肪性肝病(NAFLD)、酒精性肝病(ALD)以及病毒性肝炎感染,HCC的发病率一直在上升。各种局部区域治疗(LRTs)用于治疗HCC,包括热消融、经动脉治疗、立体定向体放疗(SBRT)和经动脉放射栓塞(TARE)。传统的反应评价标准,如WHO和RECIST,依赖于基于大小的测量,可能无法准确评估对lrt的治疗反应。为了解决这一局限性,已经开发了实体肿瘤的改进反应评估标准(mRECIST)和LI-RADS治疗反应算法(LR-TRA)。mRECIST评估患者水平的反应,而LR-TRA专门针对lrt治疗的HCC提供病变水平的反应评估。本文讨论HCC的影像学诊断方法及不同lrt后病变的影像学表现。它解释了分类治疗反应的标准,如LR-TR可行,LR-TR不可行和LR-TR模棱两可。它还强调了反应评估的挑战和未来方向,包括辅助结果的结合,接受局部和全身联合治疗的患者的评估,以及血清AFP、AFP- l3和PIVKA-II等生物标志物的潜在使用。总之,局部治疗扩大了HCC的治疗选择,准确的疗效评估对于优化患者管理至关重要。mRECIST和LR-TRA为评估治疗反应提供了有价值的工具,未来的更新有望解决具体的挑战,并纳入像iRECIST和定量成像评估这样的新方法。此外,生物标志物的使用可能会补充未来基于成像的反应评估。
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Response Assessment of Treated Hepatocellular Carcinoma
Abstract Hepatocellular carcinoma (HCC) is a leading cause of morbidity and mortality worldwide, including in India. The incidence of HCC has been rising due to lifestyle diseases such as obesity, diabetes, non-alcoholic fatty liver disease (NAFLD), and alcoholic liver disease (ALD), as well as viral hepatitis infections. Various locoregional therapies (LRTs) are used to treat HCC, including thermal ablation, transarterial therapies, stereotactic body radiotherapy (SBRT), and transarterial radioembolization (TARE). Traditional response evaluation criteria like WHO and RECIST, which rely on size-based measurements, may not accurately assess treatment response to LRTs. To address this limitation, modified response evaluation criteria for solid tumors (mRECIST) and the LI-RADS treatment response algorithm (LR-TRA) have been developed. mRECIST assesses patient-level response, while LR-TRA provides lesion-level response assessment specifically for HCC treated with LRTs. This article discusses the imaging protocols for diagnosing HCC and the imaging appearances of treated lesions after different LRTs. It explains the criteria for categorizing treatment response, such as LR-TR viable, LR-TR non-viable, and LR-TR equivocal. It also highlights the challenges and future directions in response assessment, including the incorporation of ancillary findings, the assessment of patients receiving a combination of locoregional and systemic therapies, and the potential use of biomarkers like serum AFP, AFP-L3, and PIVKA-II. In conclusion, locoregional therapies have expanded the treatment options for HCC, and accurate response assessment is crucial for optimizing patient management. mRECIST and LR-TRA provide valuable tools for evaluating treatment response, and future updates are expected to address specific challenges and incorporate newer approaches like iRECIST and quantitative imaging assessment. Additionally, the use of biomarkers may complement imaging-based response assessment in the future.
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