Tumor mutational burden
The correlations of tumor mutational burden among single-region tissue, multi-region tissues and blood in non-small cell lung cancer
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Use of targeted next generation sequencing to characterize tumor mutational burden and efficacy of immune checkpoint inhibition in small cell lung cancer
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Designing gene panels for tumor mutational burden estimation: the need to shift from ‘correlation’ to ‘accuracy’
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Tumor mutational burden quantification from targeted gene panels: major advancements and challenges
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<p>Tumor Mutational Burden and PD-L1 Expression in Non-Small-Cell Lung Cancer (NSCLC) in Southwestern China</p>
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PD-L1 expression and tumor mutational burden are independent biomarkers in most cancers
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Genomic landscape and its correlations with tumor mutational burden, PD-L1 expression, and immune cells infiltration in Chinese lung squamous cell carcinoma
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Biomarkers of immunotherapy in urothelial and renal cell carcinoma: PD-L1, tumor mutational burden, and beyond
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PD-L1 expression and tumor mutational burden status for prediction of response to chemotherapy and targeted therapy in non-small cell lung cancer
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Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden
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Predicting response to checkpoint inhibitors in melanoma beyond PD-L1 and mutational burden
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Persistent mutant oncogene specific T cells in two patients benefitting from anti-PD-1
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Extraskeletal myxoid chondrosarcoma with massive pulmonary metastases
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Significance and implications of FDA approval of pembrolizumab for biomarker-defined disease
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Differential immune profiles distinguish the mutational subtypes of gastrointestinal stromal tumor
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Genomics of response to immune checkpoint therapies for cancer: implications for precision medicine
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The degree of intratumor mutational heterogeneity varies by primary tumor sub-site
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PARP inhibitors: Synthetic lethality in the clinic.
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Bioluminescence imaging and two-photon microscopy guided laser ablation of GBM decreases tumor burden
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TP53 mutation variant allele frequency is a potential predictor for clinical outcome of patients with lower-risk myelodysplastic syndromes
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