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MedNeXt: Transformer-driven Scaling of ConvNets for Medical Image Segmentation

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arxiv 2303.09975 v5 pith:WVECNU5S submitted 2023-03-17 eess.IV cs.CVcs.LG

classification eess.IVcs.CVcs.LG
keywords medicalsegmentationimagekernelmednextarchitectureconvnextperformance
verification ladder T0 review T1 audit T2 compute T3 formal
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There has been exploding interest in embracing Transformer-based architectures for medical image segmentation. However, the lack of large-scale annotated medical datasets make achieving performances equivalent to those in natural images challenging. Convolutional networks, in contrast, have higher inductive biases and consequently, are easily trainable to high performance. Recently, the ConvNeXt architecture attempted to modernize the standard ConvNet by mirroring Transformer blocks. In this work, we improve upon this to design a modernized and scalable convolutional architecture customized to challenges of data-scarce medical settings. We introduce MedNeXt, a Transformer-inspired large kernel segmentation network which introduces - 1) A fully ConvNeXt 3D Encoder-Decoder Network for medical image segmentation, 2) Residual ConvNeXt up and downsampling blocks to preserve semantic richness across scales, 3) A novel technique to iteratively increase kernel sizes by upsampling small kernel networks, to prevent performance saturation on limited medical data, 4) Compound scaling at multiple levels (depth, width, kernel size) of MedNeXt. This leads to state-of-the-art performance on 4 tasks on CT and MRI modalities and varying dataset sizes, representing a modernized deep architecture for medical image segmentation. Our code is made publicly available at: https://github.com/MIC-DKFZ/MedNeXt.

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Cited by 1 Pith paper

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. F3-Net: Foundation Model for Full Abnormality Segmentation of Medical Images with Flexible Input Modality Requirement

    cs.CV 2025-07 reject novelty 3.0 of 10

    F3-Net combines multi-encoder nnU-Net with zero-filled missing modalities to segment glioma, metastasis, stroke, and white matter lesions, but the missing-modality claim is untested and comparisons are incomplete.

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