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Integration of Clinical Trial Spatial Multiomics Analysis and Virtual Clinical Trials Enables Immunotherapy Response Prediction and Biomarker Discovery.
Zhang, Shuming; Deshpande, Atul; Verma, Babita K; Wang, Hanwen; Mi, Haoyang; Yuan, Long; Ho, Won Jin; Jaffee, Elizabeth M; Zhu, Qingfeng; Anders, Robert A; Yarchoan, Mark; Kagohara, Luciane T; Fertig, Elana J; Popel, Aleksander S.
Afiliación
  • Zhang S; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Deshpande A; Bloomberg-Kimmel Immunotherapy Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Verma BK; Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Wang H; Convergence Institute, Johns Hopkins University, Baltimore, Maryland.
  • Mi H; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Yuan L; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Ho WJ; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Jaffee EM; Bloomberg-Kimmel Immunotherapy Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Zhu Q; Department of Immunology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Anders RA; Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Yarchoan M; Convergence Institute, Johns Hopkins University, Baltimore, Maryland.
  • Kagohara LT; Bloomberg-Kimmel Immunotherapy Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Fertig EJ; Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Popel AS; Convergence Institute, Johns Hopkins University, Baltimore, Maryland.
Cancer Res ; 84(16): 2734-2748, 2024 Aug 15.
Article en En | MEDLINE | ID: mdl-38861365
ABSTRACT
Due to the lack of treatment options, there remains a need to advance new therapeutics in hepatocellular carcinoma (HCC). The traditional approach moves from initial molecular discovery through animal models to human trials to advance novel systemic therapies that improve treatment outcomes for patients with cancer. Computational methods that simulate tumors mathematically to describe cellular and molecular interactions are emerging as promising tools to simulate the impact of therapy entirely in silico, potentially greatly accelerating delivery of new therapeutics to patients. To facilitate the design of dosing regimens and identification of potential biomarkers for immunotherapy, we developed a new computational model to track tumor progression at the organ scale while capturing the spatial heterogeneity of the tumor in HCC. This computational model of spatial quantitative systems pharmacology was designed to simulate the effects of combination immunotherapy. The model was initiated using literature-derived parameter values and fitted to the specifics of HCC. Model validation was done through comparison with spatial multiomics data from a neoadjuvant HCC clinical trial combining anti-PD1 immunotherapy and a multitargeted tyrosine kinase inhibitor cabozantinib. Validation using spatial proteomics data from imaging mass cytometry demonstrated that closer proximity between CD8 T cells and macrophages correlated with nonresponse. We also compared the model output with Visium spatial transcriptomics profiling of samples from posttreatment tumor resections in the clinical trial and from another independent study of anti-PD1 monotherapy. Spatial transcriptomics data confirmed simulation results, suggesting the importance of spatial patterns of tumor vasculature and TGFß in tumor and immune cell interactions. Our findings demonstrate that incorporating mathematical modeling and computer simulations with high-throughput spatial multiomics data provides a novel approach for patient outcome prediction and biomarker discovery.

Significance:

Incorporating mathematical modeling and computer simulations with high-throughput spatial multiomics data provides an effective approach for patient outcome prediction and biomarker discovery.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biomarcadores de Tumor / Carcinoma Hepatocelular / Inmunoterapia / Neoplasias Hepáticas Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biomarcadores de Tumor / Carcinoma Hepatocelular / Inmunoterapia / Neoplasias Hepáticas Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article