A computer aided chromosome imaging technique for cancer diagnosis

用于癌症诊断的计算机辅助染色体成像技术

• 批准号: 7423851
• 负责人: Hong Liu
• 金额: $ 31.27万
• 依托单位: UNIVERSITY OF OKLAHOMA
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-14 至 2011-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7423851
• 关键词: Algorithms; Belief; Biological Neural Networks; Cancer Prognosis; Cells; Chromosome Pairing; Chromosome abnormality; Chromosomes; Chromosomes, Human, Pair 3; Classification; Clinical; Computer Assisted; Computer software; Computer-Assisted Diagnosis; Computers; Congenital chromosomal disease; Cultured Tumor Cells; Custom; Cytogenetics; Databases; Deletion Mutation; Diagnosis; Diagnostic; Disease; Doctor of Philosophy; Effectiveness; Future; Genetic; Genetic Programming; Graph; Hematologic Neoplasms; Hour; Human; Image; Imaging Techniques; Intervention; Label; Laboratories; Location; Low Prevalence; Machine Learning; Malignant - descriptor; Malignant Neoplasms; Metaphase; Methods; Microscope; Microscopic; Molecular; Monitor; Morphology; Normal Cell; Numbers; Patients; Pattern; Performance; Physicians; Process; Rate; Receiver Operating Characteristics; Recurrence; Research; Research Personnel; Resolution; S-Phase Fraction; Sampling; Scanning; Scheme; Skin; Slide; Solutions; Speed; Staging; System; Techniques; Technology; Testing; Therapeutic; Time; Training; Treatment Efficacy; base; cancer cell; cancer diagnosis; cancer therapy; cancer type; clinical Diagnosis; clinical application; computerized; concept; day; design; detector; digital imaging; experience; improved; innovation; interest; leukemia; malignant breast neoplasm; novel; outcome forecast; programs; size; tool; user-friendly

DESCRIPTION (provided by applicant): Identification of recurrent chromosomal aberrations is important for diagnosis, prognosis, and therapy of most hematological malignancies. Due to difficulties with culture of tumor cells, low mitotic index, poor chromosomal morphologies, and low prevalence, it takes tremendous effort and time for a cytogenetic clinician to obtain a sufficient number of analyzable metaphase cells under microscope before he/she can make an accurate clinical diagnosis. This process is not only very inefficient but also subject to human errors. In order to improve the efficiency and accuracy of leukemia diagnosis, we propose to develop a computer aided chromosome imaging technique. Specifically, we will develop an innovative high-speed microscopic imaging system based on a time-delay-integration technique. The system can scan the entire sample-slide at high magnification to obtain high resolution digital images to reveal metaphase chromosomes as required by clinical diagnosis. We will also develop a novel computer aided diagnosis (CAD) scheme including four specific modules to (1) detect analyzable metaphase chromosome cells, (2) segment overlapped chromosomes, (3) identify and classify distorted chromosomes associated with cancer cells, and (4) predict the cancer prognosis. After identification and segmentation of analyzable chromosomes, we will compute and search for the effective and robust image features. Genetic algorithm will be used to train and optimize an artificial neural network and a Bayesian belief network for the classification and prediction tasks, respectively. Using the integrated CAD workstation, we will conduct an observer performance study to assess the performance of the technique and its clinical feasibility. In summary, the proposed imaging technique is highly efficient, and no or only minimal human interventions are required from initial slide-scanning up to the presentation of CAD results. With such a new computerized clinical tool, cytogeneticists can effectively focus their efforts on analyzing/verifying chromosomal abnormal patterns and making final diagnostic decisions. It is therefore expected that the proposed technology can significantly improve the efficiency and accuracy of cancer (i.e., leukemia) diagnosis. The proposed technique has significant clinical potentials in monitoring therapeutic efficacy of cancer treatment as well.

描述（由申请人提供）：复发性染色体畸变的识别对于大多数血液恶性肿瘤的诊断、预后和治疗很重要。由于肿瘤细胞培养困难、有丝分裂指数低、染色体形态差、患病率低，细胞遗传学临床医生需要付出巨大的努力和时间才能在显微镜下获得足够数量的可分析中期细胞，才能做出准确的诊断。临床诊断。这个过程不仅效率很低，而且容易出现人为错误。为了提高白血病诊断的效率和准确性，我们建议开发计算机辅助染色体成像技术。具体来说，我们将开发一种基于延时积分技术的创新高速显微成像系统。该系统可以高倍率扫描整个样本载玻片，以获得高分辨率数字图像，从而根据临床诊断的需要揭示中期染色体。我们还将开发一种新颖的计算机辅助诊断（CAD）方案，包括四个特定模块，以（1）检测可分析的中期染色体细胞，（2）分段重叠染色体，（3）识别和分类与癌细胞相关的扭曲染色体，以及（4） ）预测癌症预后。在对可分析染色体进行识别和分割后，我们将计算和搜索有效且鲁棒的图像特征。遗传算法将用于分别训练和优化用于分类和预测任务的人工神经网络和贝叶斯信念网络。使用集成 CAD 工作站，我们将进行观察者性能研究，以评估该技术的性能及其临床可行性。总之，所提出的成像技术非常高效，从最初的幻灯片扫描到 CAD 结果的呈现，不需要或只需要很少的人工干预。有了这种新的计算机化临床工具，细胞遗传学家可以有效地集中精力分析/验证染色体异常模式并做出最终的诊断决策。因此，预计所提出的技术可以显着提高癌症（即白血病）诊断的效率和准确性。所提出的技术在监测癌症治疗的疗效方面也具有显着的临床潜力。