Papillary thyroid carcinoma with a high tumor mutation burden has a poor prognosis
Male
DNA Mutational Analysis
Computational Biology
Kaplan-Meier Estimate
Middle Aged
Prognosis
3. Good health
Gene Expression Regulation, Neoplastic
03 medical and health sciences
Lymphocytes, Tumor-Infiltrating
0302 clinical medicine
Thyroid Cancer, Papillary
Databases, Genetic
Mutation
Biomarkers, Tumor
Humans
Regression Analysis
Female
Thyroid Neoplasms
DOI:
10.1016/j.intimp.2020.107090
Publication Date:
2020-10-19T17:58:07Z
AUTHORS (10)
ABSTRACT
Tumor mutation burden (TMB) as a prognostic marker for immunotherapy has shown prognostic value in many cancers. However, there is no systematic investigation on TMB in papillary thyroid carcinoma (PTC).Based on the somatic mutation data of 487 PTC patients from The Cancer Genome Atlas (TCGA), TMB was calculated, and we classified the samples into high-TMB (H-TMB) and low-TMB (L-TMB) groups. Bioinformatics methods were used to explore the characteristics and potential mechanism of TMB in PTC.High TMB predicts shorter progression-free survival (PFS) (P < 0.001). TMB was positively correlated with age, stage, tumor size, metastasis, the male sex and tall cell PTC. Compared to the L-TMB group, the H-TMB group presented with lower immune cell infiltration, a higher proportion of tumor-promoting immune cells (M0 macrophages, activated dendritic cells and monocytes) and a lower proportion of antitumor immune cells (M1 macrophages, CD8+ T cells and B cells). Additionally, the characteristics displayed by different TMB groups were not driven by critical driver mutations such as BRAF and RAS.PTC patients with high TMB have a worse prognosis. By stratifying PTC patients according to their TMB, advanced PTC patients who are candidates for immunotherapy could be selected.
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CITATIONS (12)
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