Wikipedia

Liquid biopsy

A liquid biopsy, also known as fluid biopsy or fluid phase biopsy, is the sampling and analysis of non-solid biological tissue, primarily blood.[1][2] Like traditional biopsy, this type of technique is mainly used as a diagnostic and monitoring tool for diseases such as cancer, with the added benefit of being largely non-invasive. Liquid biopsies may also be used to validate the efficiency of a cancer treatment drug by taking multiple samples in the span of a few weeks. The technology may also prove beneficial for patients after treatment to monitor relapse.[3]

Liquid biopsy
SynonymsFluid biopsy
Purposeanalysis of non-solid biological tissue

The clinical implementation of liquid biopsies is not yet widespread but is becoming standard of care in some areas.[4]

Liquid biopsy refers to the molecular analysis in biological fluids of nucleic acids, subcellular structures, especially exosomes, and, in the context of cancer, circulating tumor cells.[5]

Types

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There are several types of liquid biopsy methods; method selection depends on the condition that is being studied.

Disease Tissue sampled Sampling procedure Invasiveness Substance isolated Isolation and detection method Analysis Refs
Cancer (various) Blood Phlebotomy Minimally invasive Circulating tumor cells (CTCs) Various (e.g. CellSearch, RosetteStep, Dynabeads) Flow cytometry, nucleic acid extraction, immunocytochemistry, functional assays [6][7][8][9]
Cancer (various) Blood Phlebotomy Minimally invasive Circulating tumor DNA (ctDNA) DNA extraction Next-generation sequencing [10][11][12]
Urothelial carcinoma Urine Urine collection Non-invasive Urinary tumor DNA (utDNA) DNA extraction Next-generation sequencing [13][14]
Non-urological cancers Urine Urine collection Non-invasive Urine proteins, metabolites HPLC-MS Proteomics, metabolomics [15][16]
Bladder and prostate cancer Urine Urine collection Non-invasive Exfoliated cancer cells Urinalysis Fluorescence in situ hybridization [17][18]
Heart attack Blood Phlebotomy Minimally invasive Circulating endothelial cells (CECs) Various (e.g. CellSearch, HD-CEC) Flow cytometry [19]
Neurological diseases Cerebrospinal fluid Lumbar puncture Invasive CSF proteins, nucleic acids Various ELISA, multiplex assay, next-generation sequencing [20][21]
Prenatal diagnosis Blood (maternal) Phlebotomy Minimally invasive Cell-free fetal DNA (cffDNA) DNA extraction Karyotyping, fluorescent in situ hybridization [22]
Prenatal diagnosis Blood (maternal) Phlebotomy Minimally invasive Fetal cells in maternal blood (FCMB) Flow cytometry Karyotyping, fluorescent in situ hybridization [23]
Prenatal diagnosis Blood (umbilical cord) Cordocentesis Invasive Umbilical blood cells and molecules Various Karyotyping, blood typing, blood tests, Kleihauer–Betke test, flow cytometry [24]
Prenatal diagnosis Amniotic fluid Amniocentesis Invasive Amniotic fluid cells and molecules Various Karyotyping, blood typing, L/S ratio, S/A ratio [25]

A wide variety of biomarkers may be studied to detect or monitor other diseases. For example, isolation of protoporphyrin IX from blood samples can be used as a diagnostic tool for atherosclerosis.[26] Cancer biomarkers in the blood include PSA (prostate cancer), CA19-9 (pancreatic cancer) and CA-125 (ovarian cancer).

Mechanism

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Main articles: Circulating tumor cell § Detection methods, and Circulating tumor DNA § Analysis of ctDNA

Circulating tumor DNA (ctDNA) refers to DNA released by cancerous cells into the blood stream.[27][28] Cancer mutations in ctDNA mirror those found in traditional tumor biopsies, which allows them to be used as molecular biomarkers to track the disease.[29][30] These tests can have sensitive limits of detection, allowing monitoring of minimal residual disease after treatment. Scientists can purify and analyze ctDNA using next-generation sequencing (NGS) or PCR-based methods such as digital PCR.[31] NGS-based methods provide a comprehensive view of a cancer’s genetic makeup and is especially useful in diagnosis while digital PCR offers a more targeted approach especially well-suited for detecting minimal residual disease and for monitoring treatment response and disease progression.[32][33] Recent progress in epigenetics has expanded the use of liquid biopsy for the detection of early-stage cancers, including by approaches such as Cancer Likelihood in Plasma (CLiP) .[34]

Liquid biopsies can detect changes in tumor burden months or years before conventional imaging tests can, making them suitable for early tumor detection, monitoring, and detection of resistance mutations.[35][36][37] The increase in the adoption of NGS in various research fields, advancement in NGS, and increase in the adoption of personalized medicine are expected to drive growth in the global liquid biopsy market.[38]

Clinical application

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In cancer, liquid biopsy can be used for either multi-cancer screening tests,[39] when solid tumor biopsies are not possible, to compare different treatments as part of clinical trials, to inform decisions for doctors/patients on which precision medicine treatment to select, and for minimal residual disease detection (disease monitoring). Liquid biopsy of circulating tumor DNA for EGFR-mutated lung cancer is approved by the FDA.[40]

The CellSearch method for enumeration of circulating tumor cells in metastatic breast, metastatic colon, and metastatic prostate cancer has been validated and approved by the FDA as a useful prognostic method.[41]

See also

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References

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  1. ^ Alix-Panabières, Catherine; Pantel, Klaus (January 2013). "Circulating tumor cells: liquid biopsy of cancer". Clinical Chemistry. 59 (1): 110–118. doi:10.1373/clinchem.2012.194258. ISSN 1530-8561. PMID 23014601.
  2. ^ Crowley, Emily; Di Nicolantonio, Federica; Loupakis, Fotios; Bardelli, Alberto (9 July 2013). "Liquid biopsy: monitoring cancer-genetics in the blood". Nature Reviews Clinical Oncology. 10 (8): 472–484. doi:10.1038/nrclinonc.2013.110. PMID 23836314. S2CID 25537784.
  3. ^ "Understanding cancer's unruly origins helps early diagnosis". The Economist. September 14, 2017. Retrieved 2017-09-29.
  4. ^ Gingras, Isabelle; Salgado, Roberto; Ignatiadis, Michail (November 2015). "Liquid biopsy: will it be the 'magic tool' for monitoring response of solid tumors to anticancer therapies?". Current Opinion in Oncology. 27 (6): 560–567. doi:10.1097/CCO.0000000000000223. PMID 26335664. S2CID 13339984.
  5. ^ "Liquid Biopsy - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2023-11-08.
  6. ^ Peeters, D J E; De Laere, B; Van den Eynden, G G; Van Laere, S J; Rothé, F; Ignatiadis, M; Sieuwerts, A M; Lambrechts, D; Rutten, A; van Dam, P A; Pauwels, P; Peeters, M; Vermeulen, P B; Dirix, L Y (April 2013). "Semiautomated isolation and molecular characterisation of single or highly purified tumour cells from CellSearch enriched blood samples using dielectrophoretic cell sorting". British Journal of Cancer. 108 (6): 1358–1367. doi:10.1038/bjc.2013.92. PMC 3619252. PMID 23470469.
  7. ^ Agerbæk, Mette Ø.; Bang-Christensen, Sara R.; Yang, Ming-Hsin; Clausen, Thomas M.; Pereira, Marina A.; Sharma, Shreya; Ditlev, Sisse B.; Nielsen, Morten A.; Choudhary, Swati; Gustavsson, Tobias; Sorensen, Poul H.; Meyer, Tim; Propper, David; Shamash, Jonathan; Theander, Thor G.; Aicher, Alexandra; Daugaard, Mads; Heeschen, Christopher; Salanti, Ali (December 2018). "The VAR2CSA malaria protein efficiently retrieves circulating tumor cells in an EpCAM-independent manner". Nature Communications. 9 (1): 3279. Bibcode:2018NatCo...9.3279A. doi:10.1038/s41467-018-05793-2. PMC 6095877. PMID 30115931.
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  12. ^ Avanzini S, Kurtz DM, Chabon JJ, Moding EJ, Hori SS, Gambhir SS, Alizadeh AA, Diehn M, Reiter JG (December 2020). "A mathematical model of ctDNA shedding predicts tumor detection size". Science Advances. 6 (50): eabc4308. Bibcode:2020SciA....6.4308A. doi:10.1126/sciadv.abc4308. PMC 7732186. PMID 33310847. S2CID 228096858.
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  17. ^ Halling, Kevin C.; Kipp, Benjamin R. (September 2008). "Bladder Cancer Detection Using FISH (UroVysion Assay)". Advances in Anatomic Pathology. 15 (5): 279–286. doi:10.1097/PAP.0b013e3181832320. ISSN 1072-4109.
  18. ^ Eskra, Jillian N.; Rabizadeh, Daniel; Mangold, Leslie; Fabian, Elizabeth; Brennen, W. Nathaniel; Yeater, David B.; Pienta, Kenneth J.; Partin, Alan W.; Isaacs, William B.; Pavlovich, Christian P.; Luo, Jun (2020-08-20). "A novel method for detection of exfoliated prostate cancer cells in urine by RNA in situ hybridization". Prostate Cancer and Prostatic Diseases. 24 (1): 220–232. doi:10.1038/s41391-020-00272-6. ISSN 1365-7852.
  19. ^ Bethel, Kelly; Luttgen, Madelyn S; Damani, Samir; Kolatkar, Anand; Lamy, Rachelle; Sabouri-Ghomi, Mohsen; Topol, Sarah; Topol, Eric J; Kuhn, Peter (9 January 2014). "Fluid phase biopsy for detection and characterization of circulating endothelial cells in myocardial infarction". Physical Biology. 11 (1): 016002. Bibcode:2014PhBio..11a6002B. doi:10.1088/1478-3975/11/1/016002. PMC 4143170. PMID 24406475.
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  24. ^ Weiner, Carl P.; Lee, Gene T. (2017). "Cordocentesis". In Apuzzio, Joseph J.; Vintzileos, Anthony M.; Berghella, Vincenzo; Alvarez-Perez, Jesus R. (eds.). Operative Obstetrics, 4E. Routledge. doi:10.1201/9781315382739. ISBN 978-1-4987-2056-4.
  25. ^ Perni, Sriram C.; Roost, John R.; Chervenak, Frank A. (2017). "Amniocentesis". In Apuzzio, Joseph J.; Vintzileos, Anthony M.; Berghella, Vincenzo; Alvarez-Perez, Jesus R. (eds.). Operative Obstetrics, 4E. Routledge. doi:10.1201/9781315382739. ISBN 978-1-4987-2056-4.
  26. ^ Nascimento da Silva, Monica; Sicchieri, Letícia Bonfante; Rodrigues de Oliveira Silva, Flávia; Andrade, Maira Franco; Courrol, Lilia Coronato (2014). "Liquid biopsy of atherosclerosis using protoporphyrin IX as a biomarker". The Analyst. 139 (6): 1383–8. Bibcode:2014Ana...139.1383N. doi:10.1039/c3an01945d. PMID 24432352. S2CID 25707729.
  27. ^ "What is circulating tumor DNA and how is it used to diagnose and manage cancer?: MedlinePlus Genetics". medlineplus.gov. Retrieved 2021-09-03.
  28. ^ "What is circulating tumor DNA and how is it used to diagnose and manage cancer? ". National Institutes of Health Genetics Home Reference. 5 March 2019. Retrieved 12 March 2019.
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  30. ^ "Cell-free DNA as a biomarker in cancer". Extracell Vesicles Circ Nucleic Acid. Aug 2022. Retrieved 04 Aug 2022.
  31. ^ Picher, Andy."Liquid Biopsy, Key for Precision Medicine". Genetic Engineering & Biotechnology News. 23 July 2018. Retrieved 12 March 2019.
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  34. ^ van der Pol Y, Mouliere F (2019). "Toward the early detection of cancer by decoding the epigenetic and environmental fingerprints of cell-free DNA". Cancer Cell. 36 (4): 350–368. doi:10.1016/j.ccell.2019.09.003. PMID 31614115.
  35. ^ McDowell, Sandy."Liquid Biopsies: Past, Present, and Future". American Cancer Society. 12 February 2018. Retrieved 12 March 2019.
  36. ^ "Liquid Biopsy: Using DNA in Blood to Detect, Track, and Treat Cancer". National Cancer Institute. 8 November 2017. Retrieved 12 March 2019.
  37. ^ Olsson, Eleonor; Winter, Christof (2015). "Serial monitoring of circulating tumor DNA in patients with primary breast cancer for detection of occult metastatic disease". EMBO Molecular Medicine. 7 (8): 1034–1047. doi:10.15252/emmm.201404913. PMC 4551342. PMID 25987569.
  38. ^ "Liquid Biopsy Market - A Global and Regional Analysis: Focus on Offering, Usage, Workflow, Circulating Biomarker, Sample, Technology, Clinical Application, End User, and Region - Analysis and Forecast, 2022-2032". bisresearch.com. Retrieved 2022-09-19.
  39. ^ Brito-Rocha, Tiago; Constâncio, Vera; Henrique, Rui; Jerónimo, Carmen (18 March 2023). "Shifting the Cancer Screening Paradigm: The Rising Potential of Blood-Based Multi-Cancer Early Detection Tests". Cells. 12 (6): 935. doi:10.3390/cells12060935. ISSN 2073-4409. PMC 10047029. PMID 36980276.
  40. ^ Kwapisz, Dorota (February 2017). "The first liquid biopsy test approved. Is it a new era of mutation testing for non-small cell lung cancer?". Annals of Translational Medicine. 5 (3): 46. doi:10.21037/atm.2017.01.32. ISSN 2305-5839. PMC 5326656. PMID 28251125.
  41. ^ Karachaliou, N; Mayo-de-Las-Casas, C; Molina-Vila, MA; Rosell, R (March 2015). "Real-time liquid biopsies become a reality in cancer treatment". Annals of Translational Medicine. 3 (3): 36. doi:10.3978/j.issn.2305-5839.2015.01.16. PMC 4356857. PMID 25815297.
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