Evaluation of HCC Response to Systemic Therapy with Quantitative MRI

定量 MRI 评估 HCC 对全身治疗的反应

• 批准号: 8759420
• 负责人: Bachir Taouli
• 金额: $ 8.16万
• 依托单位: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-02-05 至 2018-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8759420
• 关键词: Algorithms; American; Angiogenesis Inhibitors; BAY 54-9085; Blood Vessels; Brain Neoplasms; Carbogen; Cellularity; Chemoembolization; Chronic Hepatitis C; Cirrhosis; Clinical; Country; Data; Data Quality; Development; Diffusion; Diffusion weighted imaging; Disease Progression; Early treatment; Evaluation; Excision; Fibrosis; Gadolinium; Goals; Growth; Health; Health Care Costs; Histologic; Histopathology; Human; Hypoxia; Image; Incidence; Infection; Investigational Therapies; Keratin-19; Liver; Liver diseases; Liver parenchyma; Mammary Neoplasms; Measurement; Measures; Metastatic Neoplasm to the Liver; Methods; Metric; Modeling; Molecular; Molecular Target; Monitor; Morbidity - disease rate; Motion; Necrosis; Outcome; Oxygen; Pathway interactions; Patients; Perfusion; Perfusion Weighted MRI; Pharmaceutical Preparations; Play; Primary carcinoma of the liver cells; Prospective Studies; Prostatic Neoplasms; Quality Control; Reaction Time; Reproducibility; Research Personnel; Role; Source; Staging; Stimulus; System; Systemic Therapy; Techniques; Testing; Therapeutic; Training; Tumor Biology; Tumor Markers; United States; Validation; Vascular Endothelial Growth Factors; Weight; Work; angiogenesis; base; blood oxygen level dependent; blood perfusion; density; effective therapy; experience; gadolinium oxide; hypoxia inducible factor 1; imaging modality; improved; liver imaging; liver injury; mortality; non-invasive system; novel; outcome forecast; research study; response; response marker; screening; tool; tumor; tumor progression; uptake

DESCRIPTION (provided by applicant): The incidence of hepatocellular carcinoma (HCC) has recently increased in the United States. HCC is/will be the source of enormous health care costs and morbidity/mortality, and generally develops in patients with advanced liver damage (advanced fibrosis and cirrhosis). Although imaging plays a major role in HCC screening and staging, the possibility of predicting HCC tumor grade, aggressiveness, angiogenesis and hypoxia with imaging are unmet needs. In addition, new antiangiogenic drugs now available to treat advanced HCC necessitate the use of new imaging criteria beyond size. In this proposal, we would like to test and validate non invasive magnet resonance imaging (MRI) methods based on advanced diffusion-weighted imaging (intravoxel incoherent motion diffusion MRI: IVIM DWI), BOLD (blood oxygen level dependent) MRI and perfusion-weighted imaging (PWI, using gadolinium contrast) to be used as non invasive markers of major histopathologic features of HCC (grade, aggressiveness, angiogenesis and hypoxia), and to predict and assess early response of HCC to systemic therapy with sorafenib (systemic drug approved for use in advanced HCC). We also would like to develop quality control tools to improve the quality and decrease variability of these quantitative MRI metrics. Based on our recent preliminary data, we believe that DWI has potential for predicting HCC tumor grade, and HCC response to locoregional therapy; and that BOLD MRI and PWI can be used to quantify degree of vascularity and lack of oxygen supply (hypoxia) in HCC, which are important tumor markers, and could be used as early markers of response to sorafenib. Ultimately, we are hoping to validate a novel non invasive algorithm based on multiparametric MRI to predict response of HCC to sorafenib, and to predict prognosis. These methods could become useful tools for testing new antiangiogenic drugs and experimental therapies in HCC, will enable individualized therapy, and provide prognosis in patients with HCC. This will be a highly significant progress in HCC and liver diseases given the increased burden of HCC in this country, and would benefit a large number of Americans over the next decade.

描述（由申请人提供）：肝细胞癌（HCC）的发病率最近在美国有所增加。HCC是/将是巨大的医疗保健成本和发病率/死亡率的来源，并且通常在具有晚期肝损伤（晚期纤维化和肝硬化）的患者中发展。虽然成像在HCC筛查和分期中起着重要作用，但利用成像预测HCC肿瘤分级、侵袭性、血管生成和缺氧的可能性是未满足的需求。此外，新的抗血管生成药物，现在可用于治疗晚期肝癌需要使用新的成像标准以外的大小。在这项提案中，我们希望测试和验证基于先进扩散加权成像的非侵入性磁共振成像（MRI）方法（体素内非相干运动扩散MRI：IVIM DWI），粗体（血氧水平依赖性）MRI和灌注加权成像（PWI，使用钆对比剂）用作HCC主要组织病理学特征的非侵入性标记物（分级、侵袭性、血管生成和缺氧），并预测和评估HCC对索拉非尼（批准用于晚期HCC的全身性药物）全身治疗的早期反应。我们还希望开发质量控制工具，以提高质量，减少这些定量MRI指标的变异性。基于我们最近的初步数据，我们认为DWI具有预测HCC肿瘤分级和HCC对局部治疗的反应的潜力; BOLD MRI和PWI可用于量化HCC中的血管分布和缺氧（缺氧）程度，这是重要的肿瘤标志物，并可用作索拉非尼反应的早期标志物。最终，我们希望验证一种基于多参数MRI的新型非侵入性算法，以预测HCC对索拉非尼的反应，并预测预后。这些方法可能成为测试新的抗血管生成药物和肝癌实验疗法的有用工具，将实现个性化治疗，并为肝癌患者提供预后。这将是HCC和肝脏疾病的一个非常重要的进展，因为HCC在这个国家的负担增加，并将在未来十年内使大量美国人受益。