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Learning Non-rigid Deformations for Robust, Constrained Point-based Registration in Image-Guided MR-TRUS Prostate Intervention

机译:学习非刚性变形,用于鲁棒,受到影响的基于点的重点,在图像引导的MR-TRUS前列腺介入中

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Accurate and robust non-rigid registration of pre-procedure magnetic resonance (MR) imaging to intra-procedure trans-rectal ultrasound (TRUS) is critical for image-guided biopsies of prostate cancer. Prostate cancer is one of the most prevalent forms of cancer and the second leading cause of cancer-related death in men in the United States. TRUS-guided biopsy is the current clinical standard for prostate cancer diagnosis and assessment. State-of-the-art, clinical MR-TRUS image fusion relies upon semi-automated segmentations of the prostate in both the MR and the TRUS images to perform non-rigid surface-based registration of the gland. Segmentation of the prostate in TRUS imaging is itself a challenging task and prone to high variability. These segmentation errors can lead to poor registration and subsequently poor localization of biopsy targets, which may result in false-negative cancer detection. In this paper, we present a non-rigid surface registration approach to MR-TRUS fusion based on a statistical deformation model (SDM) of intra-procedural deformations derived from clinical training data. Synthetic validation experiments quantifying registration volume of interest overlaps of the PI-RADS parcellation standard and tests using clinical landmark data demonstrate that our use of an SDM for registration, with median target registration error of 2.98 mm, is significantly more accurate than the current clinical method. Furthermore, we show that the low-dimensional SDM registration results are robust to segmentation errors that are not uncommon in clinical TRUS data. (C) 2017 Elsevier B.V. All rights reserved.
机译:准确且坚固的非刚性注册预过程磁共振(MR)成像与过程内的反肠超声(TRUS)是关键的前列腺癌的图像引导活组织检查。前列腺癌是美国最普遍普遍的癌症形式之一,是美国男性中癌症相关死亡的第二个主要原因之一。 TRUS引导的活检是前列腺癌诊断和评估目前的临床标准。最先进的,临床MR-TRUS图像融合依赖于MR和TRUS图像中前列腺的半自动分割,以执行腺体的非刚性表面的配准。 TRUS成像中前列腺的分割本身就是一个具有挑战性的任务,容易变化。这些分割误差可能导致登记差,随后对活检靶点的定位差,这可能导致假阴性癌症检测。在本文中,我们基于临床训练数据的过程变形的统计变形模型(SDM)向MR-TRUS融合提供了非刚性表面配准方法。合成验证实验量化利息的注册量与使用临床地标数据的PI-RADS局部标准和测试的测试略重叠,表明我们使用SDM进行登记,具有2.98 mm的中位数目标登记误差,比目前的临床方法更准确。此外,我们表明,低维SDM注册结果对于在临床TRUS数据中不常见的分割误差是强大的。 (c)2017 Elsevier B.v.保留所有权利。

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