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The Liquid Biopsy for Lung Cancer: State of the Art, Limitations and Future Developments

Daniel Di CapuaDepartment of Histopathology, St. James’s Hospital, D08NHY1 Dublin, IrelandDara Bracken‐ClarkeDepartment of Medical Oncology, St. James’ Hospital, D08NHY1 Dublin, IrelandKarine RonanFaculty of Medicine, University College Dublin, D04V1W8 Dublin, IrelandAnne‐Marie BairdSchool of Medicine, Trinity Translational Medicine Institute, Trinity College, D02PN40 Dublin, IrelandStephen P. FinnDepartment of Histopathology, St. James’s Hospital, D08NHY1 Dublin, Ireland
2021en
ABI

Аннотация

Lung cancer is a leading cause of cancer-related deaths, contributing to 18.4% of cancer deaths globally. Treatment of non-small cell lung carcinoma has seen rapid progression with targeted therapies tailored to specific genetic drivers. However, identifying genetic alterations can be difficult due to lack of tissue, inaccessible tumors and the risk of complications for the patient with serial tissue sampling. The liquid biopsy provides a minimally invasive method which can obtain circulating biomarkers shed from the tumor and could be a safer alternative to tissue biopsy. While tissue biopsy remains the gold standard, liquid biopsies could be very beneficial where serial sampling is required, such as monitoring disease progression or development of resistance mutations to current targeted therapies. Liquid biopsies also have a potential role in identifying patients at risk of relapse post treatment and as a component of future lung cancer screening protocols. Rapid developments have led to multiple platforms for isolating circulating tumor cells (CTCs) and detecting circulating tumor DNA (ctDNA); however, standardization is lacking, especially in lung carcinoma. Additionally, clonal hematopoiesis of uncertain clinical significance must be taken into consideration in genetic sequencing, as it introduces the potential for false positives. Various biomarkers have been investigated in liquid biopsies; however, in this review, we will concentrate on the current use of ctDNA and CTCs, focusing on the clinical relevance, current and possible future applications and limitations of each.

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