Open access peer-reviewed chapter

Current Advances in Clinical Application of Liquid Biopsy

By Shawn Baldacchino

Submitted: January 16th 2021Reviewed: January 19th 2021Published: March 11th 2021

DOI: 10.5772/intechopen.96086

Downloaded: 291


Liquid biopsy solutions are available for niche clinical applications. The patient benefits of such solutions are evident: ease of sampling, acceptable and repeatable. To date a number of solutions have received regulatory approval with more comprehensive, multi-cancer companion diagnostic approaches receiving approval in late 2020. Given these breakthrough advances and the ongoing clinical studies in early detection of cancer, the liquid biopsy field is making strides in technology. While circulating tumour DNA (ctDNA) solutions are quickly penetrating the market, strides in circulating tumour cells (CTC) and extracellular vesicles (EV) technologies is unlocking their potential for liquid biopsy. ctDNA solutions are paving the way towards clinical translation into the distinct applications across the cancer continuum. This chapter presents a detailed review of current approved liquid biopsy tests and provides a summary of advanced-stage prospective technologies within the context of distinctive clinical applications.


  • circulating tumour cells
  • CTC
  • extracellular vesicles
  • EV
  • cfDNA
  • ctDNA
  • methylation
  • liquid biopsy
  • cancer screening
  • precision medicine
  • companion diagnostics

1. Introduction

Precision medicine is driven by discoveries in cancer biology that enable targeted therapy against specific oncogenic molecular targets. Using small selective inhibitory molecules or monoclonal antibodies, therapies aim to effectively target tumour cells with minor effects on normal cells [1]. Targeted therapies significantly contribute to improved cancer survival, however the results have not been commensurate with expectations [2]. Tumours accumulate mutations, many of which are passenger or dispensable aberrations that can be bypassed to confer resistance. Malignant cells interact and exploit their immediate and distant microenvironment. Tumours exhibit clonal evolution that results in heterogeneity [3, 4]. Cancer is a cell disorder characterised not only by its genetics but transcriptomic, proteomic expression patterns and cellular interactions. This is driving an integrative approach to cancer diagnosis and therapeutic options [5, 6, 7].

Until recently, precision medicine was limited to the solid tissue space but is now becoming established in the liquid biopsy field with several approved solutions (Tables 1 and 2). The broad term, liquid biopsy, alludes to a test or series of tests that can provide information comparable and potentially beyond the limits of the tissue biopsy harnessing body fluid constituents. Body fluids investigated for liquid biopsy applications are comprehensive including but not limited to blood, urine [16], cerebrospinal fluid [23], stool [24], breast milk [25], saliva/sputum, oesophageal brushing, Pap smears/brushing [26], tears [27], pleural effusion [28] and ascitic fluid [29].

Single Cancer Indication
Test (Manufacturer)TechnologyBiomarkerCancer TypeApprovalApplicationSample
CellSearch® (Menarini Silocon Biosystems)CTC immuno-isolation and detection by immune-fluorescenceCTC with CD45-, EpCAM+ and (CK8, 18 and/or 19)Metastatic Breast, Colorectal, ProstateFDA / CE-IVDPrognosticBlood
Cobas® EGFR mutation test V2 (Roche)PCREGFRNSCLCFDACDxPlasma
Therascreen (Qiagen)PCR
  • PIK3CA

  • Breast

  • KRAS

  • CRC

  • BRAF

  • CRC

  • EGFR


  • FGFR

  • Urothelial

Target Selector™ (Biocept) [8]Switch-Blocker, qPCR, NGSEGFRNSCLCCE-IVDCDxBlood / FFPE
OncoBEAM (Sysmex)Digital PCRKRAS & NRASmCRCCE-IVDCDxPlasma
Idylla (Biocartis)PCR
  • KRAS

  • mCRC


  • mCRC

HCCBlood Test (Epigenomics AG) [9]Bisulfite converted DNA & PCRSEPT9 methylationHCC (patients with liver cirrhosis)CE-IVDDiagnostic aidPlasma
Epi proColon® (Epigenomics AG) [10, 11]Bisulfite converted DNA & PCRSEPT9 methylationCRCFDA / CE-IVDAncillary ScreeningPlasma
COLOGUARD (ExactSciences) [12]QuARTS & ImmunoassayBMP3 & NDRG4 methylation, KRAS, ACTB HaemoglobinCRC or advanced adenomaFDAAncillary screeningStool
IntPlex® (DiaDx) [13, 14]PCR
  • BRAF

  • mCRC

  • EFGR

  • mCRC

Xpert® Bladder Cancer Detection Xpert® Bladder Cancer Monitor (Cepheid) [15]RT-PCRUPK1B, IGF2, CRH, ANXA10, ABL1Bladder (patients with haematuria)
CE-IVDDiagnostic aid
Surveillance for recurrence
(Abbott) [16]
FISHAneuploidy 3,7,17 and loss of 9p21 (p16)Bladder (patients with haematuria)FDA / CE-IVDDiagnostic aidUrine
PCRFGFR3 and TERT PCRNMIBC (patients with haematuria)CE-IVDDiagnostic aid, Surveillance for recurrenceUrine
(Nucleix) [17]
Methylation-sensitive restriction Enzyme digestion, PCR15 DNA methylation markersBladderCE-IVDSurveillance for recurrenceUrine

Table 1.

Overview of current approved (FDA/IVD) ctDNA liquid biopsy solutions for single cancer indications.

Table provides a general overview and may not be exhaustive [CDx: Companion diagnostic; mCRC: metastatic colorectal carcinoma; CTC: Circulating tumour cells; ddPCR: droplet digital Polymerase chain reaction; FDA: Food & Drug Administration; FISH: Fluorescent in situ hybridisation; HCC: Hepatocellular carcinoma; CE-IVD: In vitro Diagnostic device certification; NMIBC: Non-muscle invasive bladder cancer; NSCLC: Non-small cell lung carcinoma; PCR: Polymerase chain reaction; QuARTS: Quantitative allele-specific real-time target and signal amplification; RT-PCR: reverse transcription PCR] [18, 19].

Pan-Cancer / Multi-cancer Indication
Test (Manufacturer)TechnologyBiomarkerCancer TypeApprovalApplicationSample
FoundationOne Liquid CDx (FoundationOne) [20]NGS
(324 genes)


  • BRCA1/2

  • Ovarian

  • BRCA1/2 & ATM

  • Prostate

  • PIK3CA

  • Breast

Guardant360 (Guardant Health) [21, 22]NGS
(73 genes)
  • Tumour mutation profiling

  • Any solid tumour

  • EGFR


Table 2.

Overview of current approved (FDA/IVD) ctDNA liquid biopsy solutions indicated for use with 2 or more solid cancers.

Table provides a general overview and may not be exhaustive. [CDx: Companion diagnostic; mCRC: metastatic colorectal carcinoma; FDA: Food & Drug Administration; NGS: Next-generation sequencing; NSCLC: Non-small cell lung carcinoma] [18, 19].

Liquid biopsy testing may encompass investigations of circulating tumour DNA (ctDNA) or cell-free DNA (cfDNA) and RNA (ctRNA), circulating tumour cells (CTCs), tumour-derived extracellular vesicles (EVs) and tumour-educated platelets [30]. Rapidly advancing technologies for immunoprofiling of leukocytes and T-cell receptor (TCR) profiling also present a potential liquid biopsy tool with a particular role in metastatic cancer patients for immunotherapy [31, 32].

The potential applications of liquid biopsy are numerous and throughout the cancer journey:

  1. Cancer detection for screening or earlier detection [33, 34],

  2. Diagnosis / Prognosis/Predictive (Companion Diagnostics, CDx) [30],

  3. Therapeutic response monitoring (Detection of resistance mechanisms) [35, 36],

  4. Minimal Residual Disease detection [37],

  5. Post-remission surveillance to predict/detect relapse, metastases and clonal evolution [37, 38].

The main advantages of a liquid biopsy assay relate to the ease of sampling. Collecting the sample is generally not invasive and repeatable enabling longitudinal monitoring. The risk of complications and pain from sample collection is minimal presenting a very acceptable procedure that beckons better uptake as a screening procedure. Liquid biopsy methods are less laborious than tissue biopsy methods and can be analysed in a much shorter time-frame (Figure 1). Moreover, liquid biopsies offer an overall snapshot of the tumour which represents distinct tumour clones, mitigating tumour region selection bias [30]. Monitoring cancer over time also provides insight on the temporal heterogeneity, a potential tool to study mechanisms of response and resistance [32, 39].

Figure 1.

Comparison of workflows of emerging liquid biopsy tools with routine cancer diagnostics by tissue biopsy. Liquid biopsy solutions remain complimentary to the clinical standard of care. [CTC: Circulating tumour cells; EVs: Extracellular vesicles; ctDNA: Circulating tumour DNA; FISH: Fluorescent in situ hybridisation; H&E: Haematoxylin and eosin; IHC: Immunohistochemistry; TAT: Turn-around time; created].

Following is a review of the advances of liquid biopsy in the context of the current state of tissue molecular pathology for clinical application. A brief illustration of future prospects is also described based on ongoing clinical studies.


2. Molecular pathology: overcoming challenges for solid and liquid biopsy

Challenges to comprehensively characterise cancer in the clinical setting exist, relating to pre-analytical (sample collection & processing), analytical and post-analytical factors. Molecular pathology of solid cancer on formalin-fixed paraffin embedded (FFPE) tissue presents technical challenges arising from tissue fixation and processing but also sample availability.

A study evaluating factors for next-generation sequencing (NGS) testing failure showed that on average 22.5% of cases do not meet quality requirements. Insufficient tissue or insufficient DNA accounted for 62% and 29% of failures with 6% failing at library preparation [40]. The study highlights increased failure from fine needle aspirates and biopsy specimens with a low failure rate in excisional specimens (1.7%) [41]. Whole genome sequencing approaches show non-uniform coverage in FFPE DNA samples resulting in sub-optimal somatic copy number alteration detection. Nonetheless clinically actionable variants are generally detected [42]. Sensitive NGS applications require good quality DNA to achieve adequate assay performance and coverage. Recent developments in DNA extraction methods and optimisation improve assay performance [42, 43]. In fact NGS solutions have been achieving regulatory approval such like Oncomine Dx (ThermoFisher Scientific) for targeted therapies in non-small cell lung carcinoma (NSCLC) [44]; Praxis (Illumina) characterising 56 KRAS/NRAS mutations for colorectal cancer companion diagnostics (CDx); Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT), the first U.S. Food & Drug Administration (FDA) approved tissue profiling test that detecting aberrations across 341 cancer genes for solid cancer tissue diagnostics but not prescriptive for any specific therapeutic product [45]; and FoundationOne CDx which is the first FDA-approved broad CDx test that is clinically and analytically validated for all solid tumours for therapeutic indication and has a success rate of >95% on FFPE [46].

Targeted gene panels or single gene polymerase chain reaction (PCR) assays are more easily translated to clinical application given their very specific intended use. Recent advances can mitigate the effects of DNA fragmentation and PCR inhibition [47]. Technical challenges are greater for detection of RNA signatures due to high degree of RNA fragmentation and introduced technical bias [48]. A study assessing the performance of PCR on RNA derived from FFPE reports that only 50% (37/74) of samples were informative. RNA profiling on FFPE samples requires alternative technologies that can robustly detect degraded RNA with reduced technical bias [49, 50, 51].

Liquid biopsy options involve far less sample processing and better sample quality. Nonetheless tumour signatures are generally rare, similar to finding ‘the needle in a haystack’, and assays require high sensitivity to avoid false negative results. In the search for a sensitive, specific and reliable method, liquid biopsy technologies are becoming more diverse and complex [52, 53, 54]. Moreover, pre-analytical considerations are critical to ensure high sensitivity and reproducible performance. These requirements vary depending on the analysed liquid biopsy component. Expert recommendations for minimal requirements for clinical cfDNA testing have been published to emphasise the need for standardisation of the test processes [55].


3. Current state of liquid biopsy application

3.1 Liquid biopsy for companion diagnostics

A particular study of previously untreated metastatic non-small cell lung carcinoma (NSCLC) shows that cfDNA technologies have the potential to detect guideline-recommended biomarkers with a higher sensitivity compared to standard of care tissue genotyping methodology [22]. Currently, ctDNA assays are being recommended for use in lung patients with progression of secondary clinical resistance and in some clinical settings where tissue is limited or insufficient for molecular testing. ctDNA assays are not recommended for the diagnosis of primary lung tumours [56]. ctDNA liquid biopsy solutions are currently approved as additional tools to the standard of care and when results are negative, tissue testing is recommended when available. Lung cancer tissue is not easily available and sampling implies potential serious complications such as pneumothorax, haemorrhage and respiratory failure. Only 50% of cases in the MarkER Identification Trial (MERIT) trial had sufficient sample for the planned molecular analyses [40]. This presents a clinical need for liquid biopsy to potentially identify a route for targeted treatment.

Advanced-stage technologies within the liquid biopsy field harness ctDNA. These approaches mainly focus on hallmark mutations or other changes in the DNA (methylation). The first FDA approved ctDNA liquid biopsy was the cobas® EGFR mutation test V2 (Roche) as a companion diagnostic [57]. This was followed by several other targeted panel companion diagnostics (Table 1). The main available plasma liquid biopsy solutions detect mutations in clinically actionable biomarkers that predict response to specific targeted therapies. The main biomarkers detected are EGFR, FGFR, KRAS, NRAS, BRAF and PIK3CA.

Selected diagnostic panels are useful as companion diagnostics for clinical trials and patient selection for specific targeted therapeutics. Nonetheless, established targets would then be integrated into larger diagnostic panels that provide a comprehensive and exhaustive approach to cancer diagnostics. Recently the FDA approved the first two NGS-based liquid biopsy solutions: Guardant360 (August, 2020) and FoundationOne CDx (November 2020) (Table 2). Unlike PCR-based targeted panels, large NGS panel tests interrogate a large-set of genes generating more clinically useful information but present a challenge to validate and regulate [58]. Similar to tissue-based NGS approaches, generated clinical information assists the definition of a spectrum of potential therapeutic options to identify a sequence of treatments to achieve optimised response [59]. In contrast, to tissue biopsy molecular analysis, liquid biopsy solutions are expected to generate a collective picture of cancer heterogenous clones enabling a comprehensive therapeutic approach which may be key to avoid clonal residual disease or recurrence [60].

A recent study evaluated the post-progression ctDNA (Guardant360 assay) with matched multiple lesion biopsies to assess heterogeneity during acquired resistance [61]. This study reveals distinct mutational profiles across metastatic lesions of gastrointestinal origin. The majority of private alterations across lesions could be detected by cfDNA. In another study, combined analysis of solid (192 genes) and liquid biopsies (27 genes) (OncoSTRAT&GO™, OncoDNA, Gosselies, Belgium), only found 40% of variants to be shared between the solid and liquid biopsy, with 51% of variants being exclusive to tissue and 9% to blood [62]. The liquid exclusive variants increased to 14% after a year from tissue sampling reflecting temporal heterogeneity [62]. The disparity in mutation calling may be a result of distinct shedding rates across tumour stage and types or sensitivity of the ctDNA assay. Although further studies are needed, such studies suggest that liquid biopsy can complement tissue molecular pathology to improve the detection of clinically actionable aberrations to overcome spatial and temporal heterogeneity especially in late-stage disease.

3.2 Liquid biopsy for cancer detection

Similar to CDx assays, current solutions for primary cancer diagnosis are either ancillary solutions or to be used when the routine screening/diagnostic test is not an option. Thus, liquid biopsy approaches are currently another tool that assist and improve the overall performance of cancer detection. Approved liquid biopsy solutions for bladder cancer screening and colorectal cancer screening are available (Table 1) to support current screening methods. Evidently, when standard of care investigations are not available, liquid biopsy can provide means of detection. For instance, Epi proColon® (Epigenomics) is available only to patients who are unwilling or unable to be screened by recommended methods. This can potentially improve screening uptake with current colorectal cancer screening uptake reported between 53 and 61% [63, 64, 65]. The more acceptable, repeatable advantages of liquid biopsy enable multi-line testing or triage testing to select patients for further investigation, similar to the faecal immunochemical testing (FIT) to the colonoscopy procedure. Cologuard (ExactSciences) offers an approved stool molecular test for the detection of colorectal cancer with a reported increased sensitivity for detecting any stage CRC (92%) and 42% sensitivity for advanced precancerous lesions [12]. Specific cases presenting positive Cologuard test and negative follow-up colonoscopy raised concerns for lack of recommendations for patient management in these scenarios [66].

A first-line or triage test should be cost-effective, especially for screening purposes, to achieve a net cost–benefit. A recent health technology assessment evaluates EGFR T790M resistance mutation testing in patients with advanced NSCLC can lead to fewer tissue biopsies although a follow-up confirmatory tissue biopsy is required when liquid biopsy tests negative [67]. EGFR T790M mutation detection from urine has also been shown to be feasible for NSCLC patients to reduce biopsy procedures and mitigate biopsy related complications [68].

In a similar approach, the ExoDx Prostate test (ExosomeDx, a Bio-Techne brand), can be used to assess cancer risk in patients with elevated prostate specific antigen (PSA) to assist the decision to proceed or defer a prostate biopsy. ExoDx is the first exosome-based (RNA biomarkers) liquid biopsy solution to receive a Breakthrough Device Designation by the U.S. FDA [69]. Prostate cancer screening by PSA has highlighted the risks of over diagnosis and over treatment accompanied by a lack of tangible benefit [70, 71]. This created a need to better inform clinical decisions to follow-up with invasive diagnostic procedures and treatment and accentuates the need for sensitive tests that are also highly specific. Specific clinical applications require performance parameters that balance risk of non-detection with overtreatment depending on the backbone standard of care tests.

3.3 Liquid biopsy for prognosis and therapy intervention

CellSearch® (Menarini Silicon Biosystems), a CTC detection system, was the first liquid biopsy approach to be approved by FDA in 2004. The CellSearch technology immunomagnetically captures CTCs from whole blood, that express the Epithelial cell adhesion molecule (EpCAM) and enumerates CTCs with the profile of CD45 negative and cytokeratin 8, 18, and/or 19 positive [72]. The CellSearch system provides prognostic information for patients with metastatic breast, prostate or colorectal cancer. A major limitation of this method is the reliance on the EpCAM marker. CTCs have been described to be heterogeneous and not all CTCs express EpCAM. Such methods are restrictive to the epithelial phenotype and have intrinsic selection bias [73]. Label-free CTC enrichment solutions, such as Parsortix® (ANGLE) and ClearCell® FX1 system (Biolidics) are European CE marked as in vitrodiagnostic device (CE-IVD) solutions for CTC enrichment but require downstream analysis to derive clinically relevant information. Moreover, isolated CTC remain viable and can potentially be cultured and studied further although finding optimal conditions for culturing CTC subtypes is challenging [74]. CTC enrichment by size discrimination shows a reduced recovery rate (~60%) for smaller sized cell lines (SKBR3) [75] presenting with a selective enrichment and failing to detect a subset of cells similarly to immunoisolation methods. CTC enrichment by depletion of leukocytes also results in reduced recovery [76]. Current advances in flow cytometry resolution and imaging may enable the suppression of pre-enrichment to enable a quick and efficient detection of CTC [77, 78, 79]. These approaches have a definite role in therapeutic monitoring, identifying treatment response and early resistance and are ready for clinical studies [80, 81].

ctDNA abundance, mutation count and a KEAP1, KRAS, MET signature predict overall survival in advanced NSCLC patients (N = 949). Interestingly, patients with at least one ctDNA clearance during the course of treatment had a significantly better progression-free survival and overall survival than patients with consistent ctDNA levels throughout treatment [82]. The prognosis and predictive potential of ctDNA is yet to be translated into practical clinical assays. While the potential role of EV in cancer prognosis has been shown [83], further studies are required to define EV isolation and prognostic correlations in larger patient cohorts.


4. Current outlook for early cancer detection

5-year survival rates for patients diagnosed with stage I and stage IV cancer respectively are 98% and 26% for breast cancer, 92% to 10% for colorectal cancer and 57% to 3% for lung cancer [84]. Earlier diagnosis would greatly improve cancer survivability but is currently a great challenge. Detecting cancer early is a cornerstone of the UK’s NHS Long term plan. There have been numerous efforts to achieve early cancer screening, through public awareness (Be Clear on Cancer and Detect Cancer Early campaigns), introducing new screening tests (Bowel screening) and targeted lung health checks (following the NELSON trial) and many more.

Complex approaches, by GRAIL [85], Thrive’s CancerSEEK [86], FoundationMedicine, Base Genomics, Freenome aim to expand the potential of early diagnosis from blood. Grail’s Galleri, Thrive’s CancerSEEK and Natera’s Signatera have achieved FDA Breakthrough device status while in the trial stage. Early diagnosis remains a challenge with sensitivity being a critical factor. Achieving early diagnosis in the blood using ctDNA is more complex, mainly because there is a huge amount of “normal” DNA circulating in the blood. The smaller the cancer the smaller and less detectible the cancer signature is in the blood. As any cancer grows, it sheds more DNA, more cellular debris and more cancer cells into the bloodstream which eventually leads to the cancer spreading to distant organs. Although the ctDNA shedding rate can vary among patients, a mathematical model can predict tumour size by assessing haploid genome equivalents per plasma volume (correlation: R2 = 0.32; P = 2.6x10–16) [87]. The smaller the tumour, the higher the probability of a false negative result for a particular actionable mutation.

Till date there is no FDA-approved solution for early cancer detection from blood with targeted panel solutions available as ancillary diagnostics from stools for colorectal cancer (ColoGuard & Epi ProColon) and from urine for bladder cancer (Xpert Bladder Cancer detection & Uromonitor). Interestingly, a blood test detecting Septin 9 (SEPT9) methylation to aid the detection of hepatocellular carcinoma (HCC) in patients with cirrhosis, has been CE-IVD marked (HCCBloodTest by Epigenomics) [9].

Following are some illustrative examples of ongoing clinical studies investigating the application of liquid biopsy for multi-cancer detection.

4.1 CancerSEEK, PapSEEK, UroSEEK

A series of liquid biopsy tests for early diagnosis have been developed at the Johns Hopkins University: CancerSEEK, PapSEEK and UroSEEK.

CancerSEEK measures 8 protein biomarkers by immunoassays and mutations on 16 genes by PCR and sequencing in blood samples to detect and localise the cancer. A study of eight cancer types (colorectal, ovary, pancreas, breast, upper gastrointestinal tract, lung and liver) resulted in a median sensitivity of 70%, ranging from 33% in breast and 98% in ovarian cancer. Across stages of the disease the test was 43%, 73% and 78% sensitive respectively [86]. In a following prospective, interventional study (DETECT-A) CancerSEEK was coupled with positron emission tomography– computed tomography (PET-CT) for cancer detection. During this trial, the blood test sensitivity for all cancer types was 27.1% and specificity of 98.9%. Of note, 108 participants out of 10,006 in this study had a positive blood test without cancer, most of who (101) were followed up by PET-CT and 38 also had a subsequent procedure to rule out cancer [34]. This highlights the importance of the high specificity levels required for potential screening tests and clearly defined second-line testing with a good consideration of the risk of overtreatment.

PapSEEK was developed for Pap brush samples or Tao brush samples and detects aneuploidy and somatic mutations on 18 genes by multiplex-PCR (AKT1, APC, BRAF, CDKN2A, CTNNB1, EGFR, FBXW7, FGFR2, KRAS, MAPK1, NRAS, PIK3CA, PIK3R1, POLE, PPP2R1A, PTEN, RNF43, and TP53). 81% endometrial cancer and 29% ovarian cancer were detected by PapSEEK on Pap brush samples which increased to 93% and 45% respectively when intrauterine samples were collected using a Tao brush. False positive rate was 1.4% for Pap brush samples which improved to >99% specificity when using the Tao brush [88].

UroSEEK detects mutations within 11 genes (FGFR3, TP53, CDKN2A, ERBB2, HRAS, KRAS, PIK3CA, MET, VHL, MLL, TERT promoter) as well as aneuploidy. In an early detection cohort UroSEEK was 83% sensitive and 93% specific while in the surveillance cohort sensitivity was 71% and specificity 80% which was a significant improvement compared to cytology alone [89].

4.2 Galleri

Recently, the UK’s National Health Service (NHS) has taken bold steps and will be partnering with GRAIL to confirm Galleri’s clinical and economic performance in the NHS system [90]. The study will investigate the effectiveness of the Galleri test on 140,000 asymptomatic, healthy patients and 25,000 participants showing signs and symptoms of cancer. The Galleri test is a genome-wide test interrogating methylation patterns in plasma samples, optimised during the The Circulating Cell-free Genome Atlas Study (CCGA). Methylation patterns, measured by whole genome-bisulfite sequencing, were found to perform better than whole genome and targeted (507genes) sequencing for the detection of cancer [85]. A further study to evaluate the performance of the optimised method, included 6,689 participants with more than 50 cancer types which were approximately equally distributed across stage of the disease (I- IV). The test achieved 99.3% specificity and 55.2% sensitivity across all cancers in the validation sets. Sensitivity improved when detecting more advanced cancer, reporting a detection of 39% of Stage I cancer, 69% of Stage II cancer and 83–92% sensitivity in Stage III & IV cancer. Cancer detection performance varied across different cancer types [85].

Such clinical studies represent landmark studies that paving the way for clinical service to initiate the introduction of liquid biopsy technologies for cancer screening.


5. Potential for EVs and integrative solutions

Tumour derived extracellular vesicles (EV) show great potential for liquid biopsy. EVs carry protein, DNA, RNA and small-RNA cargo shielding it from degradation [33, 91]. The cargoes carried by EVs represents a molecular fingerprint of the cell of origin [30]. A study comparing cfDNA and EV DNA in pleural effusion for EGFR testing by qPCR, shows an improved detection rate when using EV DNA (72.2% vs. 61.1%) [28]. Moreover, research has described that 90% of prostate cancer ctDNA is found in large EVs [92]. EVs are released in abundant quantities presenting an intriguing solution for increase detection sensitivity [30]. TearExo® is a potential solution detecting EV diagnostic and prognostic markers from tears for diagnosis of breast cancer [27].

Despite these advantages, implementation of EVs into clinical cancer diagnostics is hampered by challenges and lack of standardisation in the isolation methods and analytical sensitivity [93]. With improved and standardised technologies and focused efforts, tumour EVs can potentially be used to selectively pick out tumour-derived DNA from a background of normal DNA enhancing ctDNA technology sensitivity but also enable analysis of DNA, RNA and protein from the same sample, potentially for yet earlier detection.

Several challenges remain to be elucidated. EV populations are diverse and the functions and contents of EVs across their size distribution is not well known. The shedding rates across different tumour types or disease states are cannot be assessed without a standardised and accurate method for sizing and specific size isolation. Several concerted efforts are leading the way to technical standardisation to robustly understand the role of EVs [93, 94].

Solutions that integrate multi-modal testing are budding, such as Epic Sciences’ Comprehensive cancer profiling that performs CTC, ctDNA and immune-cell analysis from a single blood draw relying characterising protein, morphology and genomics. CancerSEEK integrates protein markers with ctDNA analysis. Such approaches may be key to unlock the full potential of liquid biopsies but present technical, workflow and interpretation challenges [95].


6. Conclusion

Liquid biopsy is currently a clinically useful tool for assisting companion diagnostics, cancer screening programmes and surveillance. There is an evident prevalence of ctDNA solutions which are already available for the companion diagnostic space and are expected to be accessing the earlier diagnostic space soon following clear delineation of the clinical value and applications. CTC solutions, the first approved liquid biopsy tool for clinical use, have a role in defining cancer prognosis and therapeutic monitoring for timely and effective therapeutic decisions. The clinical value and approach remain to be defined by further clinical studies and translation into practical, clinically applicable solutions.

The full potential of EVs is being uncovered with concerted efforts to establish rigour and standardisation driving reproducible research. Apart from the role of EVs for therapeutic applications, EVs show great potential for early diagnosis of cancer, therapeutic monitoring and post-therapeutic surveillance. Versatile and open technologies could facilitate integrated solutions to maximise the potential of liquid biopsy. Nonetheless, translation to the clinical setting will require practical solutions with clearly defined clinical applications.

Promising data is emerging across potential applications for liquid biopsy with multi-cancer early detection solutions expected in the near future.

© 2021 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Shawn Baldacchino (March 11th 2021). Current Advances in Clinical Application of Liquid Biopsy, Pathology - From Classics to Innovations, Ilze Strumfa and Guntis Bahs, IntechOpen, DOI: 10.5772/intechopen.96086. Available from:

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