解决3D肝肿瘤检测中2D切片结果碎片化问题
YOLO-PVC: 2D-to-3D Consolidation of Slice-wise Detections for Volumetric Liver Tumor Localization in MRI

- 通过分位数统计融合切片检测框,增强深度连续性
- 3D IoU达0.710,平面重叠率约0.78
- 轻量级设计,适用于临床MRI肝肿瘤定位
由于计算效率高且可扩展性强,基于切片的2D目标检测器被越来越多地用于体数据。然而,这类方法在深度方向上常产生碎片化和不稳定的预测。本文提出YOLO-PVC,一种轻量级、与模型无关的2D到3D检测融合框架。该方法通过强制深度连续性、利用稳健分位数统计聚合边界框坐标,并引入轻量级MLP校准模块优化轴向范围。相比简单的堆叠或平均策略,YOLO-PVC显式处理深度维度上的缺失检测和异常切片。在三个肿瘤类别上的3D肝部MRI实验表明,其性能持续优于多种聚合基线。启发式PVC方法实现总体3D IoU为0.665,校准版本进一步提升至0.710,平面重叠(BEV IoU)约为0.78。结果表明,结构化的几何融合是临床MRI中肝肿瘤定位的有效实用方案。
原文摘要 · Abstract (English)
Slice-wise 2D object detectors are increasingly applied to volumetric data due to their computational efficiency and scalability, yet they often yield fragmented and unstable predictions along the depth axis. We propose YOLO-PVC, a lightweight and model-agnostic framework for 2D-to-3D consolidation of slice-wise detections. The method enforces depth continuity, aggregates bounding box coordinates using robust percentile statistics, and further refines axial extent through a lightweight MLP-based calibration module. Unlike naïve stacking or averaging strategies, YOLO-PVC explicitly addresses missing detections and outlier slices along the depth dimension. Experiments on 3D liver MRI volumes across three tumor categories demonstrate consistent improvements over multiple aggregation baselines. The heuristic PVC achieves an overall $\mathrm{IoU}_{3D}$ of $0.665$, while the calibrated variant further improves performance to $0.710$, with high planar overlap ($\mathrm{BEV\ IoU} \approx 0.78$). These results demonstrate that structured geometric consolidation provides an effective and practical solution for volumetric liver tumor localization in clinical MRI.
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