A Novel Prognostic Biomarker Panel for Early-Stage Colon Carcinoma

التفاصيل البيبلوغرافية
العنوان: A Novel Prognostic Biomarker Panel for Early-Stage Colon Carcinoma
المؤلفون: Maria Luisa Gomez-Dorronsoro, Berta Ibáñez-Beroiz, Ruth Vera, María del Rosario Mercado, Pablo Azcue, Ignacio Encío, David Guerrero Setas
المساهمون: Universidad Pública de Navarra. Departamento de Ciencias de la Salud, Nafarroako Unibertsitate Publikoa. Osasun Zientziak Saila
المصدر: Cancers; Volume 13; Issue 23; Pages: 5909
Cancers
Academica-e. Repositorio Institucional de la Universidad Pública de Navarra
instname
Cancers, Vol 13, Iss 5909, p 5909 (2021)
بيانات النشر: Multidisciplinary Digital Publishing Institute, 2021.
سنة النشر: 2021
مصطلحات موضوعية: PD-L1, Oncology, Cancer Research, medicine.medical_specialty, Prognostic biomarker, Colorectal cancer, Disease, Article, GLUT-1, MUC2, e-cadherin, CDX2, CMS, colon cancer, prognostic biomarker, Internal medicine, medicine, Stage (cooking), RC254-282, Tissue microarray, biology, business.industry, E‐cadherin, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Microsatellite instability, medicine.disease, Colon cancer, GLUT‐1, PD‐L1, Cohort, biology.protein, Immunohistochemistry, business
الوصف: Simple Summary Decision about treatment choice in early-stage colon cancer may be difficult for clinicians because of a lack of published data. Colon cancer is a very heterogeneous disease, but some previous efforts have helped us elucidate potential biomarkers for characterizing patients. Our goal is to create a panel of biomarkers capable of differentiating patients with a low, medium, and high risk of death or relapse. Our results suggest that, by combining PD-L1, GLUT-1, and mismatch repair proteins in a biomarker panel, patients could be significantly and evenly divided into one of these three groups. The resulting biomarker panel has the potential clinical value that, by being able to classify a patient with early colon cancer as being at high risk of death or tumor evolution, they could benefit from a more aggressive early treatment, while this approach might not be needed for low-risk patients. Abstract Molecular characterization of colorectal cancer has helped us understand better the biology of the disease. However, previous efforts have yet to provide significant clinical value in order to be integrated into clinical practice for patients with early-stage colon cancer (CC). The purpose of this study was to assess PD-L1, GLUT-1, e-cadherin, MUC2, CDX2, and microsatellite instability (dMMR) and to propose a risk-panel with prognostic capabilities. Biomarkers were immunohistochemically assessed through tissue microarrays in a cohort of 144 patients with stage II/III colon cancer. A biomarker panel consisting of PD-L1, GLUT-1, dMMR, and potentially CDX2 was constructed that divided patients into low, medium, and high risk of overall survival or disease-free survival (DFS) in equally sized groups. Compared with low-risk patients, medium-risk patients have almost twice the risk of death (HR = 2.10 (0.99–4.46), p = 0.054), while high-risk patients have almost four times the risk (HR = 3.79 (1.77–8.11), p = 0.001). The multivariate goodness of fit was 0.756 and was correlated with Kaplan–Meier curves (p = 0.002). Consistent results were found for DFS. This study provides a critical basis for the future development of an immunohistochemical assessment capable of discerning early-stage CC patients as a function of their prognosis. This tool may aid with treatment personalization in daily clinical practice and improve survival outcomes.
وصف الملف: application/pdf
اللغة: English
تدمد: 2072-6694
DOI: 10.3390/cancers13235909
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d777bffd35a72d1b3d40d4da9b6e0843
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....d777bffd35a72d1b3d40d4da9b6e0843
قاعدة البيانات: OpenAIRE
الوصف
تدمد:20726694
DOI:10.3390/cancers13235909