LMOD+: A Comprehensive Multimodal Dataset and Benchmark for Developing and Evaluating Multimodal Large Language Models in Ophthalmology
Zhenyue Qin, Yang Liu, Yu Yin, Jinyu Ding, Haoran Zhang, Anran Li, Dylan Campbell, Xuansheng Wu, Ke Zou, Tiarnan D. L. Keenan, Emily Y. Chew, Zhiyong Lu, Yih-Chung Tham, Ninghao Liu, Xiuzhen Zhang, Qingyu Chen
TL;DR
LMOD+ delivers a comprehensive multimodal ophthalmology benchmark (32,633 instances across 12 conditions and 5 imaging modalities) to develop and evaluate generative, multimodal LLMs. By unifying data curation, providing free-text prompts, and evaluating 24 MLLMs in tasks spanning anatomical recognition, disease screening, staging, and demographic prediction, the work reveals a substantial gap between current general-domain MLLMs and ophthalmology needs, with zero-shot disease screening around 58% accuracy and disease staging remaining difficult. The substantial dataset expansion, broader task coverage, and public leaderboard offer a resource to drive domain-specific model development and reduce vision-threatening disease burden through AI. The study also highlights strong performance for some models in specific sub-tasks (e.g., anatomical recognition by InternVL variants) but overall indicates that clinical-grade ophthalmic AI will require targeted modeling and data strategies beyond zero-shot transfer.
Abstract
Vision-threatening eye diseases pose a major global health burden, with timely diagnosis limited by workforce shortages and restricted access to specialized care. While multimodal large language models (MLLMs) show promise for medical image interpretation, advancing MLLMs for ophthalmology is hindered by the lack of comprehensive benchmark datasets suitable for evaluating generative models. We present a large-scale multimodal ophthalmology benchmark comprising 32,633 instances with multi-granular annotations across 12 common ophthalmic conditions and 5 imaging modalities. The dataset integrates imaging, anatomical structures, demographics, and free-text annotations, supporting anatomical structure recognition, disease screening, disease staging, and demographic prediction for bias evaluation. This work extends our preliminary LMOD benchmark with three major enhancements: (1) nearly 50% dataset expansion with substantial enlargement of color fundus photography; (2) broadened task coverage including binary disease diagnosis, multi-class diagnosis, severity classification with international grading standards, and demographic prediction; and (3) systematic evaluation of 24 state-of-the-art MLLMs. Our evaluations reveal both promise and limitations. Top-performing models achieved ~58% accuracy in disease screening under zero-shot settings, and performance remained suboptimal for challenging tasks like disease staging. We will publicly release the dataset, curation pipeline, and leaderboard to potentially advance ophthalmic AI applications and reduce the global burden of vision-threatening diseases.
