A liquid biopsy is a broad term used to describe the collection and analysis of non-solid biological tissues derived primarily from peripheral blood. A liquid biopsy assay detects and analyses relevant tumor biomarkers utilizing mainly circulating tumor DNA (ctDNA) or circulating tumor cells (CTC)1 as the sample material. Analysis of these tumor-driven biomarkers may assist in cancer detection, treatment selection, therapy response monitoring, and studying resistance mechanisms.
In recent years, liquid biopsy has gained traction because it provides easy access to tumor-derived biomarkers with fewer potential complications for the patient compared to a surgical biopsy.
In 2016, the US-FDA approved the first liquid biopsy to aid in the detection of specific mutations in the epidermal growth factor receptor (EGFR) gene in non-small cell lung cancer (NSCLC) patients. These mutations may predict response to EGFR tyrosine kinase inhibitors1. Today, multiple commercial liquid biopsy assays have been approved in various oncological applications.
While liquid biopsy may present an attractive alternative to a solid biopsy, it also has limitations. Here, we shed light on some advantages, limitations, and future outlook for liquid biopsy in oncology clinical practice.
Solid biopsies remain the gold standard and a routine test in today's clinical practice. They enable the histological evaluation of a tumor, provide tumor staging and identify actionable genetic alterations to guide patient care. However, solid biopsies also have their limitations. First, a solid biopsy is invasive and is, in certain tumors, hard to obtain. Furthermore, a single solid biopsy might not provide a comprehensive picture of the tumor's genetic landscape, as many tumors are morphologically and genetically heterogeneous with numerous subclones.
In these cases, a liquid biopsy assay may provide an alternative and assist in identifying key genetic alterations that aid in diagnosing, treating, and monitoring periods of relapse and remission in cancer patients. Additionally, a liquid biopsy assay is easily repeated and may provide indications of ongoing metastasis and insight into the aggressive disease state.
Liquid biopsy is still a nascent technology with numerous challenges that hinder its incorporation into standard clinical practice. One disadvantage of a liquid biopsy assay is that it may miss critical genetic alterations in early disease states simply because ctDNA from a particular tumor may exist in extremely low concentrations. This may result in a delay in the diagnosis and administration of crucial life-saving therapeutics.
Furthermore, in some cases, age-related clonal hematopoiesis of indeterminate potential (CHIP) can interfere with ctDNA testing and cause incorrect interpretation of results, leading to inappropriate therapeutic decisions for patient management.
Precision medicine has revolutionized patient care and allowed a personalized approach to targeted therapeutics such as tyrosine kinase inhibitors (TKI) and immunotherapies2. These therapeutics often rely on detecting genetic alternation in tumor cells, and liquid biopsies offer real-time and easy access to the evolving tumor landscape. However, Liquid biopsies may still lack widespread clinical and commercial acceptance.
In addition, a solid biopsy will be needed for the initial histological diagnosis of a tumor. Therefore, it is unlikely that liquid biopsy will replace solid biopsy for the foreseeable future but rather be used in conjunction with a solid biopsy to refine diagnosis and monitor response to treatment.
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