Searching for Robust Augmentations to Improve Out-of-Domain Generalization in Dermoscopic Skin Cancer Classification
- URL: http://arxiv.org/abs/2607.26765v1
- Date: Wed, 29 Jul 2026 11:06:06 GMT
- Title: Searching for Robust Augmentations to Improve Out-of-Domain Generalization in Dermoscopic Skin Cancer Classification
- Abstract summary: We study how data augmentation improves robustness of a malignant binary-non-malignant generalization.<n>Data augmentation was searched on a multi-source ISIC Archive collection.
- Score: 35.18016233072556
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: Background/Objectives: Dermoscopic skin lesion classifiers often lose accuracy under domain shift across imaging devices, illumination, and capture artifacts. We study how data augmentation improves the robustness of a binary malignant-versus-non-malignant classifier, with emphasis on out-of-domain (OOD) generalization. Methods: Single augmentations, photometric combinations, and composite policies were searched on a multi-source ISIC Archive collection with Derm7pt, using a ConvNeXt-Large backbone and ROC-AUC. Splits were made at the lesion-ID level, and HAM10000 and ISIC 2019-2020 were held out as a predominantly source-disjoint OOD test. Results: The largest OOD gain came from the mix policy, and photometric transformations dominated the most useful OOD operations. On an expanded pool from the same held-out sources the gain was +0.053 (95% CI +0.045 to +0.061, p<0.001), consistent across four training seeds (per-seed ROC-AUC: baseline 0.761-0.775, mix 0.806-0.829). On a small independent clinical collection, single-checkpoint sensitivity rose from 0.591 to 0.818, but this rested on 22 malignant cases and did not persist across seeds. Conclusions: Augmentations modelling real sources of domain shift can matter more than maximizing in-domain accuracy. Because the policy was selected on the same sources used to evaluate it, a source-disjoint selection protocol is needed before this effect size can be read as unbiased.
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