Mapping of Lesion Images to Somatic Mutations

• URL: http://arxiv.org/abs/2512.02162v1
• Date: Mon, 01 Dec 2025 19:48:53 GMT
• Title: Mapping of Lesion Images to Somatic Mutations
• Authors: Rahul Mehta,
• Abstract summary: We build a deep latent variable model to determine patients' somatic mutation profiles based on their corresponding medical images.<n>We show the model's predictive performance on the counts of specific mutations as well as it's ability to accurately predict the occurrence of mutations.
• Score: 0.46533841420895894
• License: http://creativecommons.org/licenses/by/4.0/
• Abstract: Medical imaging is a critical initial tool used by clinicians to determine a patient's cancer diagnosis, allowing for faster intervention and more reliable patient prognosis. At subsequent stages of patient diagnosis, genetic information is extracted to help select specific patient treatment options. As the efficacy of cancer treatment often relies on early diagnosis and treatment, we build a deep latent variable model to determine patients' somatic mutation profiles based on their corresponding medical images. We first introduce a point cloud representation of lesions images to allow for invariance to the imaging modality. We then propose, LLOST, a model with dual variational autoencoders coupled together by a separate shared latent space that unifies features from the lesion point clouds and counts of distinct somatic mutations. Therefore our model consists of three latent space, each of which is learned with a conditional normalizing flow prior to account for the diverse distributions of each domain. We conduct qualitative and quantitative experiments on de-identified medical images from The Cancer Imaging Archive and the corresponding somatic mutations from the Pan Cancer dataset of The Cancer Genomic Archive. We show the model's predictive performance on the counts of specific mutations as well as it's ability to accurately predict the occurrence of mutations. In particular, shared patterns between the imaging and somatic mutation domain that reflect cancer type. We conclude with a remark on how to improve the model and possible future avenues of research to include other genetic domains.

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