Pansharpening in remote sensing image aims at acquiring a high-resolution multispectral (HRMS) image directly by fusing a low-resolution multispectral (LRMS) image with a panchromatic (PAN) image. The main concern is how to effectively combine the rich spectral information of LRMS image with the abundant spatial information of PAN image. Recently, many methods based on deep learning have been proposed for the pansharpening task. However, these methods usually have two main drawbacks: 1) requiring HRMS for supervised learning; and 2) simply ignoring the latent relation between the MS and PAN image and fusing them directly. To solve these problems, we propose a novel unsupervised network based on learnable degradation processes, dubbed as LDP-Net. A reblurring block and a graying block are designed to learn the corresponding degradation processes, respectively. In addition, a novel hybrid loss function is proposed to constrain both spatial and spectral consistency between the pansharpened image and the PAN and LRMS images at different resolutions. Experiments on GaoFen-2, Worldview-2 and Worldview-3 images demonstrate that our proposed LDP-Net can fuse PAN and LRMS images effectively without the help of HRMS samples, achieving promising performance in terms of both qualitative visual effects and quantitative metrics.

Delineation of brain metastases (BMs) is a paramount step in stereotactic radiosurgery (SRS) treatment. Clinical practice has specific expectation on BM auto-delineation that the method is supposed to avoid missing of small lesions and yield accurate contours for large lesions. In this study, we propose a novel coarse-to-fine framework, named detector-based segmentation (DeSeg), to incorporate object-level detection into pixel-wise segmentation so as to meet the clinical demand. DeSeg consists of three components: a center-point-guided single-shot detector (CPG-SSD) to localize the potential lesion regions, a multi-head U-Net segmentation model to refine contours, and a data cascade unit to connect both tasks smoothly. Performance on tiny lesions is measured by the object-based sensitivity and positive predictive value (PPV), while that on large lesions is quantified by dice similarity coefficient (DSC), average symmetric surface distance (ASSD) and 95% Hausdorff distance (HD95). Besides, computational complexity is also considered to study the potential of method in real-time processing. This study retrospectively collected 240 BM patients with Gadolinium injected contrast-enhanced T1-weighted magnetic resonance imaging (T1c-MRI), which were randomly split into training, validating and testing datasets (192, 24 and 24 scans, respectively). The lesions in the testing dataset were further divided into two groups based on the volume size (small S:≤1.5 cc, N=88; large L: >1.5 cc, N=15). On average, DeSeg yielded a sensitivity of 0.91 and a PPV of 0.77 on S group, and a DSC of 0.86, an ASSD 0f 0.76 mm and a HD95 of 2.31 mm on L group. The results indicated that DeSeg achieved leading sensitivity and PPV for tiny lesions as well as segmentation metrics for large ones. After our clinical validation, DeSeg showed competitive segmentation performance while kept faster processing speed comparing with existing 3D models.

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