arXiv:2609.29156v1 Announce Type: cross
Abstract: Long-tailed chest X-ray classification requires visual representations that capture both common abnormalities and subtle, infrequent findings. We propose Med-AR-8B and Med-AR-2B, two radiology-native autoregressive vision-language models pretrained with structured reports, abnormality-focused text, and region annotations. We evaluate the transfer of their visual encoders to multi-label classification against contrastive, self-supervised, and supervised pretrained encoders, including Med-CLIP, CheXFound, EVA-Base, ARK, and BioViL-T, using a common ML-Decoder classification head. To assess fine-grained recognition, we also construct LLM-expanded, report-derived label sets for MIMIC-CXR and CheXpert. Across PadChest, MIMIC-CXR, and CheXpert, Med-AR-8B outperforms Med-CLIP in mean AUROC and AUPRC for head, medium, and tail findings. On MIMIC-CXR, it increases tail-label mean AUPRC from 0.1033 to 0.1441. Med-AR-2B achieves the strongest discrimination results on PadChest. Across the broader encoder comparison, a Med-AR variant achieves the highest mean AUROC and AUPRC in every reported prevalence group on each public dataset. Both Med-AR variants also achieve lower excess area under the risk-coverage curve than Med-CLIP on all three public datasets, indicating improved selective-prediction performance under the evaluated protocol. Internal results are metric-dependent, with Med-CLIP retaining advantages in overall and tail AUPRC and in selective prediction. These findings establish Med-AR as a strong pretraining recipe for long-tailed chest X-ray classification on the evaluated public benchmarks and demonstrate the value of assessing discrimination and selective prediction together.
Abstract: Long-tailed chest X-ray classification requires visual representations that capture both common abnormalities and subtle, infrequent findings. We propose Med-AR-8B and Med-AR-2B, two radiology-native autoregressive vision-language models pretrained with structured reports, abnormality-focused text, and region annotations. We evaluate the transfer of their visual encoders to multi-label classification against contrastive, self-supervised, and supervised pretrained encoders, including Med-CLIP, CheXFound, EVA-Base, ARK, and BioViL-T, using a common ML-Decoder classification head. To assess fine-grained recognition, we also construct LLM-expanded, report-derived label sets for MIMIC-CXR and CheXpert. Across PadChest, MIMIC-CXR, and CheXpert, Med-AR-8B outperforms Med-CLIP in mean AUROC and AUPRC for head, medium, and tail findings. On MIMIC-CXR, it increases tail-label mean AUPRC from 0.1033 to 0.1441. Med-AR-2B achieves the strongest discrimination results on PadChest. Across the broader encoder comparison, a Med-AR variant achieves the highest mean AUROC and AUPRC in every reported prevalence group on each public dataset. Both Med-AR variants also achieve lower excess area under the risk-coverage curve than Med-CLIP on all three public datasets, indicating improved selective-prediction performance under the evaluated protocol. Internal results are metric-dependent, with Med-CLIP retaining advantages in overall and tail AUPRC and in selective prediction. These findings establish Med-AR as a strong pretraining recipe for long-tailed chest X-ray classification on the evaluated public benchmarks and demonstrate the value of assessing discrimination and selective prediction together.
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