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Developing an immune signature for triple-negative breast cancer to predict prognosis and immune checkpoint inhibitor response.
Wang, Ce; Feng, Guoshuang; Zhu, Jingjing; Wei, Kecheng; Huang, Chen; Wu, Zhenyu; Yu, Yongfu; Qin, Guoyou.
Afiliación
  • Wang C; Department of Biostatistics, School of Public Health, & The Key Laboratory of Public Health Safety of Ministry of Education, Fudan University, Shanghai, China.
  • Feng G; Beijing Advanced Innovation Center for Big Data-Based Precision Medicine, Beihang University & Capital Medical University, Beijing 100083, China.
  • Zhu J; Big Data & Engineering Research Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
  • Wei K; Beijing Advanced Innovation Center for Big Data-Based Precision Medicine, Beihang University & Capital Medical University, Beijing 100083, China.
  • Huang C; Department of Biostatistics, School of Public Health, & The Key Laboratory of Public Health Safety of Ministry of Education, Fudan University, Shanghai, China.
  • Wu Z; Department of Biostatistics, School of Public Health, & The Key Laboratory of Public Health Safety of Ministry of Education, Fudan University, Shanghai, China.
  • Yu Y; Department of Biostatistics, School of Public Health, & The Key Laboratory of Public Health Safety of Ministry of Education, Fudan University, Shanghai, China.
  • Qin G; Department of Biostatistics, School of Public Health, & The Key Laboratory of Public Health Safety of Ministry of Education, Fudan University, Shanghai, China.
Future Oncol ; 18(9): 1055-1066, 2022 Mar.
Article en En | MEDLINE | ID: mdl-35105171
ABSTRACT

Aim:

We aimed to develop a new signature based on immune-related genes to predict prognosis and response to immune checkpoint inhibitors in patients with triple-negative breast cancer (TNBC). Materials &

methods:

Single-sample gene set enrichment was used to develop an immune-based prognostic signature (IPRS) for TNBC patients. We conducted multivariate Cox analysis to evaluate the prognosis value of the IPRS.

Result:

An IPRS based on 66 prognostic genes was developed. Multivariate Cox analysis indicated that the IPRS was an independent factor for prognosis. PD-1, PD-L1, PD-L2 and CTLA4 gene expression was higher in the low-risk group, suggesting IPRS could predict the response to immune checkpoint inhibitors.

Conclusion:

The IPRS might be a reliable signature to predict TNBC patients' prognosis and response to immune checkpoint inhibitors, but needs prospective validation.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pronóstico / Regulación Neoplásica de la Expresión Génica / Neoplasias de la Mama Triple Negativas / Inhibidores de Puntos de Control Inmunológico Tipo de estudio: Evaluation_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Revista: Future Oncol Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pronóstico / Regulación Neoplásica de la Expresión Génica / Neoplasias de la Mama Triple Negativas / Inhibidores de Puntos de Control Inmunológico Tipo de estudio: Evaluation_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Revista: Future Oncol Año: 2022 Tipo del documento: Article País de afiliación: China