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Machine learning on syngeneic mouse tumor profiles to model clinical immunotherapy response.
Zeng, Zexian; Gu, Shengqing Stan; Wong, Cheryl J; Yang, Lin; Ouardaoui, Nofal; Li, Dian; Zhang, Wubing; Brown, Myles; Liu, X Shirley.
Afiliación
  • Zeng Z; Department of Data Science, Dana Farber Cancer Institute, Boston, MA 02215, USA.
  • Gu SS; Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02215, USA.
  • Wong CJ; Department of Data Science, Dana Farber Cancer Institute, Boston, MA 02215, USA.
  • Yang L; Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02215, USA.
  • Ouardaoui N; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
  • Li D; Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
  • Zhang W; Department of Data Science, Dana Farber Cancer Institute, Boston, MA 02215, USA.
  • Brown M; Department of Biomedical Informatics, Harvard Medical School, Boston, MA 02115 USA.
  • Liu XS; Department of Data Science, Dana Farber Cancer Institute, Boston, MA 02215, USA.
Sci Adv ; 8(41): eabm8564, 2022 Oct 14.
Article en En | MEDLINE | ID: mdl-36240281
ABSTRACT
Most patients with cancer are refractory to immune checkpoint blockade (ICB) therapy, and proper patient stratification remains an open question. Primary patient data suffer from high heterogeneity, low accessibility, and lack of proper controls. In contrast, syngeneic mouse tumor models enable controlled experiments with ICB treatments. Using transcriptomic and experimental variables from >700 ICB-treated/control syngeneic mouse tumors, we developed a machine learning framework to model tumor immunity and identify factors influencing ICB response. Projected on human immunotherapy trial data, we found that the model can predict clinical ICB response. We further applied the model to predicting ICB-responsive/resistant cancer types in The Cancer Genome Atlas, which agreed well with existing clinical reports. Last, feature analysis implicated factors associated with ICB response. In summary, our computational framework based on mouse tumor data reliably stratified patients regarding ICB response, informed resistance mechanisms, and has the potential for wide applications in disease treatment studies.

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Sci Adv Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Sci Adv Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos