Recent advances in generative models, including large language models (LLMs), vision language models (VLMs), and diffusion models, have accelerated the field of natural language and image processing in medicine and marked a significant paradigm shift in how biomedical models can be developed and deployed. While these models are highly adaptable to new tasks, scaling and evaluating their usage presents new challenges not addressed in previous frameworks. In particular, the ability of these models to produce useful outputs with little to no specialized training data ("zero-" or "few-shot" approaches), as well as the open-ended nature of their outputs, necessitate the development of updated guidelines in using and evaluating these models. In response to gaps in standards and best practices for the development of clinical AI tools identified by US Executive Order 141103 and several emerging national networks for clinical AI evaluation, we begin to formalize some of these guidelines by building on the "Minimum information about clinical artificial intelligence modeling" (MI-CLAIM) checklist. The MI-CLAIM checklist, originally developed in 2020, provided a set of six steps with guidelines on the minimum information necessary to encourage transparent, reproducible research for artificial intelligence (AI) in medicine. Here, we propose modifications to the original checklist that highlight differences in training, evaluation, interpretability, and reproducibility of generative models compared to traditional AI models for clinical research. This updated checklist also seeks to clarify cohort selection reporting and adds additional items on alignment with ethical standards.

借鉴MI-CLAIM清单，本文提出了一份更新的指南，旨在澄清临床研究中生成模型相对传统人工智能模型的训练、评估、可解释性和可重复性差异，以及与伦理标准的对齐。

更新临床人工智能最低信息（MI-CLAIM）生成建模研究清单