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测试时学习前列腺解剖结构以用于微超声中的癌症检测

Learning Prostate Anatomy at Test Time for Cancer Detection in Micro-Ultrasound

Obed Korshie Dzikunu, Mohammad Mahdi Abootorabi, Mohamed Harmanani, Paul F. R. Wilson, Emma Willis, Ferdinand Luger, Adam Kinnaird, Brian Wodlinger, Parvin Mousavi, Purang Abolmaesumi

arXiv 2608.20557首次发表:更新:

发表机构

University of British Columbia; Vector Institute; Ordensklinikum Linz; University of Alberta; Exact Imaging(不列颠哥伦比亚大学; 向量研究所; 林茨 Ordenklinikum 医院; 阿尔伯塔大学; Exact Imaging 公司)

机构由 AI 辅助整理,请以论文原文为准。

AI 中文总结

该研究针对微超声前列腺癌检测的域偏移问题,提出ANT分段引导的测试时自适应框架,在多中心临床试验数据上提升了活检芯和患者水平的AUC,优于TTA基线。

AI 中文摘要

使用不同成像硬件或采集协议的临床中心之间的域偏移,仍然是部署深度学习模型用于前列腺癌(PCa)检测的根本障碍。现有的测试时自适应(TTA)方法通过熵最小化或基于增强的自监督来解决分布偏移,校正图像外观的统计差异,但忽略了目标域的解剖结构。我们提出ANT,这是一个分段引导的TTA框架,通过在测试时解决辅助前列腺分段任务,将预训练的癌症检测编码器适配到目标域,该任务由来自冻结的预训练分段网络的伪掩码监督。通过将编码器表示与目标域的前列腺解剖结构对齐,ANT可校正特定域的特征漂移,同时保留癌症判别结构。该模型在一项多中心临床试验中,使用早期一代微超声扫描仪对693名患者成像进行训练,并在另一项临床试验中,使用新一代系统对两个中心的118名患者进行评估。在所有方法评估条件相同的留一中心协议下,与无自适应方法相比,ANT在活检芯和患者水平上分别将平均AUC提高了2.9%和3.6%,优于TTA基线。代码可在以下网址获取:this https URL。

英文摘要

Domain shift across clinical centers using different imaging hardware or acquisition protocols remains a fundamental barrier to deploying deep learning models for prostate cancer (PCa) detection. Existing test-time adaptation (TTA) methods address distribution shift through entropy minimization or augmentation-based self-supervision, correcting for statistical differences in image appearance but ignoring the anatomical structure of the target domain. We propose ANT, a segmentation-guided TTA framework that adapts a pretrained cancer detection encoder to the target domain by solving an auxiliary prostate segmentation task at test time, supervised by pseudo-masks from a frozen pretrained segmentation network. By aligning encoder representations to prostate anatomy in the target domain, ANT corrects domain-specific feature drift while preserving cancer-discriminative structure. The model was trained on 693 patients imaged with an earlier-generation micro-ultrasound scanner in a multi-center clinical trial, and evaluated on 118 patients acquired with a newer-generation system across two centers in another clinical trial. Under a leave-one-center-out protocol with identical evaluation conditions across all methods, ANT improves mean AUC by 2.9% and 3.6% at the biopsy-core and patient levels, respectively, over no adaptation, outperforming TTA baselines. Code is available at: https://github.com/ObedDzik/ant.git.

论文原文

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