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Ann Oncol ; 29(suppl_1): i38-i46, 2018 01 01.
Article in English | MEDLINE | ID: mdl-29462257

ABSTRACT

Molecular profiling has changed the treatment landscape in advanced non-small-cell lung cancer. Accurately identifying the tumours that harbour sensitizing EGFR mutations, the most common targetable molecular alteration, as well as those with acquired resistance mutations (e.g. T790M) on treatment is a high clinical priority. The current clinical gold standard is genotyping of tumour specimens. However, the practical utility of this approach is limited by the lack of available tissue and the potential complications associated with biopsies. With the advent of newer sequencing assays, it has become feasible to assess tumour genomics via a blood sample, termed a 'liquid biopsy'. In this review, we summarize the available techniques for liquid biopsies and their applicability for detecting sensitizing and resistance EGFR mutations and how these results may be used for making treatment decisions.


Subject(s)
Carcinoma, Non-Small-Cell Lung/drug therapy , Genotyping Techniques/methods , Lung Neoplasms/drug therapy , Protein Kinase Inhibitors/pharmacology , Biomarkers, Tumor/blood , Biomarkers, Tumor/genetics , Biomarkers, Tumor/metabolism , Carcinoma, Non-Small-Cell Lung/blood , Carcinoma, Non-Small-Cell Lung/genetics , Carcinoma, Non-Small-Cell Lung/pathology , Circulating Tumor DNA/blood , Circulating Tumor DNA/genetics , Clinical Decision-Making , Drug Resistance, Neoplasm/genetics , ErbB Receptors/antagonists & inhibitors , ErbB Receptors/genetics , Feasibility Studies , Humans , Liquid Biopsy/methods , Lung/pathology , Lung Neoplasms/blood , Lung Neoplasms/genetics , Lung Neoplasms/pathology , Mutation , Predictive Value of Tests , Prognosis , Protein Kinase Inhibitors/therapeutic use , Risk Assessment/methods , Treatment Outcome
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