AI Article Synopsis

  • Liquid biopsy is gaining traction in cancer research, particularly for non-small cell lung cancer (NSCLC), due to better insights into cancer drivers and resistance to treatments.
  • Current blood tests for liquid biopsy have limited sensitivity, especially when tumor volumes are low, leading to the need for confirmatory biopsies that can yield small, less useful samples for genetic testing.
  • Other body fluids besides blood, such as urine and cerebrospinal fluid, may offer richer sources of tumor DNA, enabling more effective applications of circulating tumor DNA analysis in NSCLC from early detection to metastasis.

Article Abstract

Liquid biopsy is a rapidly emerging field due to an increasing number of oncogenic drivers and a better understanding of resistance mechanisms to targeted therapies in non-small cell lung cancer (NSCLC). The sensitivity of the most widely used blood-based assays is, however, limited in particular in cases of low tumor volume where shed of tumor-derived material can be limited. A negative result thus requires biopsy confirmation using minimally invasive sampling procedures that can result in small specimens, which are often not suitable for genotyping. Liquid biopsy is not limited to plasma, and tumor DNA circulating in other body fluids such as urine, pleural fluid, cerebrospinal fluid, or cytology specimen-derived supernatant can be exploited. In comparison to cell blocks, these fluids in close contact to the tumor may contain a more abundant and less analytically demanding tumor DNA. In this review, we discuss the potential applications of circulating tumor DNA derived from cytology samples in NSCLC, from early stage (screening, nodule characterization) to metastatic disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698102PMC
http://dx.doi.org/10.3390/cells9112486DOI Listing

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