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AI-driven body composition atlas reveals its association with NSCLC immunotherapy outcome and molecular background: a multicenter study
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  • Published: 27 March 2026

AI-driven body composition atlas reveals its association with NSCLC immunotherapy outcome and molecular background: a multicenter study

  • Yusheng Guo1,2,3 na1,
  • Bingxin Gong1,2,3 na1,
  • Jie Lou1,2,3 na1,
  • Li Wan4,
  • Ying-Long Peng5,
  • Yiqun Chen6,
  • Xiaoyan Lei7,
  • Peng Mo8,
  • Qi Wan9,
  • Qing Sun1,2,3,
  • Shu Peng10,
  • Chuansheng Zheng1,2,3 &
  • …
  • Lian Yang1,2,3 

npj Precision Oncology , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biomarkers
  • Cancer
  • Computational biology and bioinformatics
  • Immunology
  • Oncology

Abstract

Although previous studies have linked body composition to immunotherapy efficacy, comprehensive multidimensional analyses with biological explanations remain lacking. This study integrated eight independent cohorts comprising 2,132 non-small cell lung cancer (NSCLC) patients, including five immune checkpoint inhibitor prognostic cohorts (n = 1,919), two bulk RNA-seq cohorts (n = 190), and one prospective single-cell RNA-seq cohort (n = 23). Using deep learning algorithms, we automatically extracted 92 body composition parameters from computed tomography images. The AI-based segmentation system demonstrated high consistency with manual measurements (intraclass correlation coefficient >0.87) with significantly improved efficiency. In male patients, higher intermuscular fat volume (IMFV) and 14 other indicators were independent predictors of overall survival; in female patients, T12 subcutaneous fat density and 6 other indicators showed potential associations with survival. Male patients with high IMFV exhibited significant upregulation of interferon-related pathways in CD8 + T cells and NK cells, along with lower exhaustion scores, while female patients with high T12 subcutaneous fat density showed macrophage polarization toward the M1 phenotype. This study underscores the importance of multidimensional body composition in NSCLC patient management, demonstrating that specific parameters are not only closely related to survival outcomes but also exhibit unique gender differences and location variations, providing new insights for optimizing immunotherapy strategies.

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Data availability

The data that support the findings of this study are available on request from the corresponding author.

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Acknowledgements

This work was supported by the Noncommunicable Chronic Diseases-National Science and Technology Major Project (2024ZD0522800/2024ZD0522806), the key project of Hubei provincial Natural Science Foundation (2023BCB014), the National Nature Science Foundation of China (No. 82172034, No. 82472058). The funders of this study had no role in study design, data collection, data analysis, data interpretation, or writing of this report.

Author information

Author notes
  1. These authors contributed equally: Yusheng Guo, Bingxin Gong, Jie Lou.

Authors and Affiliations

  1. Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

    Yusheng Guo, Bingxin Gong, Jie Lou, Qing Sun, Chuansheng Zheng & Lian Yang

  2. Hubei Provincial Clinical Research Center for Precision Radiology & Interventional Medicine, Wuhan, China

    Yusheng Guo, Bingxin Gong, Jie Lou, Qing Sun, Chuansheng Zheng & Lian Yang

  3. Hubei Key Laboratory of Molecular Imaging, Wuhan, China

    Yusheng Guo, Bingxin Gong, Jie Lou, Qing Sun, Chuansheng Zheng & Lian Yang

  4. Department of Thoracic Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

    Li Wan

  5. Guangdong Lung Cancer Institute, Guangdong Provincial People’s Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China

    Ying-Long Peng

  6. Department of Respiratory and Critical Care Medicine, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China

    Yiqun Chen

  7. Department of Radiology, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, China

    Xiaoyan Lei

  8. Department of Radiotherapy, 900th Hospital of Joint Logistics Support Force, Fuzhou, China

    Peng Mo

  9. Department of Radiology, the Key Laboratory of Advanced Interdisciplinary Studies Center, National Center for Respiratory Medicine, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

    Qi Wan

  10. Department of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

    Shu Peng

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Contributions

Y.G., B.G., and J.L. conceived the project. Y.G., B.G., J.L., Y.P., Q.S., and S.P. performed investigation. L.W., Y.C., X.L., P.M., Q.W., Q.S., and S.P. assisted in study design and data curation. Y.G., B.G., and J.L. performed data analysis. L.W. collected human samples. Y.G., B.G., and J.L. wrote the original draft of the manuscript. C.Z. and L.Y. were responsible for project management and supervision. L.W., Y.C., X.L., P.M., Q.W., Q.S., S.P., C.Z., and L.Y. reviewed and edited the manuscript. All authors have approved and reviewed the final manuscript.

Corresponding authors

Correspondence to Shu Peng, Chuansheng Zheng or Lian Yang.

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The authors declare no competing interests.

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Supplementary information

41698_2026_1382_MOESM1_ESM (download DOCX )

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Guo, Y., Gong, B., Lou, J. et al. AI-driven body composition atlas reveals its association with NSCLC immunotherapy outcome and molecular background: a multicenter study. npj Precis. Onc. (2026). https://doi.org/10.1038/s41698-026-01382-5

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  • Received: 03 December 2025

  • Accepted: 12 March 2026

  • Published: 27 March 2026

  • DOI: https://doi.org/10.1038/s41698-026-01382-5

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