Reports - Liquid Biopsy Market
Liquid Biopsy Market Size Analysis Report 2025-2035 by Product & Services (Assay Kits, Instruments, Services) by Circulating Biomarkers (Circulating Tumor Cells, Circulating Tumor DNA (ctDNA), Circulating Tumor DNA (ctDNA), Cell-free DNA (cfDNA), Extracellular Vesicles (EVS), Other Circulating Biomarkers) by Clinical Applications (Early Cancer Screening, Therapy Selection, Treatment Monitoring, Recurrence Monitoring) by Technology (Multi-Gene Parallel Analysis using NGS, Single-Gene Analysis using PCR Microarrays) by Application (Cancer Applications, Non-Cancer Applications) by Sample Type (Blood, Other Sample Types) by End User (Reference Laboratories, Hospitals & Physician Laboratories, Academic & Research Centers, Other End Users) by Region (North America, Europe, Asia Pacific, Latin America, Middle East & Africa
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USD 11.41 Billion
USD 30.65 Billion
9.41%
North America
Asia Pacific
2024
2021 - 2023
2025 - 2035
By Product & Services, By Circulating Biomarkers, By Clinical Applications , By Technology , By Application , By Sample Type, By End User , By Region
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The global Liquid Biopsy Market is valued at USD 11.41 Billion in 2024 and is projected to reach a value of USD 30.65 Billion by 2035 at a CAGR (Compound Annual Growth Rate) of 9.41% between 2025 and 2035.
Cancer is the second leading cause of death globally, and the increasing global incidence of cancer is driving the market. According to WHO, approximately 16.3 million cancer related deaths are likely to occur by 2040. Among various cancer indications, breast cancer is the most common type of cancer worldwide, followed by lung cancer, colorectal cancer, and prostate cancer. According to the SEER statistics, nearly 18% women are expected to be diagnosed with breast cancer at some point during their lifetime, with an estimated 297,790 new cases in 2023.
FDA-approved liquid biopsy tests are crucial as cancer is the leading cause for death globally. They have been thoroughly researched to ensure safety and accuracy. Several tests are in development and various stages of research, four are currently FDA-approved:
Monitoring minimal residual disease (MRD) represents a significant application in liquid biopsy. This involves using liquid biopsy techniques to detect and analyze residual cancer cells or DNA present in the bloodstream after treatment. This non-invasive method provides a valuable tool for evaluating treatment effectiveness and predicting the likelihood of cancer recurrence. The ongoing evolution of liquid biopsy technologies and their integration into clinical settings continues to propel the growth and adoption of liquid biopsy solutions for MRD monitoring. For instance, in November 2023, Illumina Inc. unveiled TruSight Oncology 500 ctDNA v2, an advanced version of its liquid biopsy assay tailored for comprehensive genomic profiling in oncology. This updated iteration boasts improved sensitivity and specificity in identifying cancer-related mutations found in circulating tumor DNA.
Cancer is the leading cause of death in Canada and the second-leading cause of death in the USA. For instance, according to the International Agency for Research on Cancer, the most prevalent types of cancer include lungs cancer, breast cancer, prostate cancer, and colorectal cancer. Cancer and other infectious diseases may occur as a result of biological and environmental risk factors, including smoking, air pollution, and tobacco use. Many cancer research institutions are aggressively using cutting-edge tactics and patient-centered approaches for early cancer diagnosis and therapy in order to meet the rising cancer burden.
The increasing incidence of genetic abnormalities among neonates and fetuses has amplified the need for prenatal testing. In order to reduce the spread of infectious diseases and chronic illnesses like cancer, government programs encouraging public screening tests have increased the use of noninvasive screening tests that use biological fluids including blood, amniotic fluid, and cerebrospinal fluid (CSF).
During the screening or recurrence stages of cancer patients' disease, these tests identify indicators of malignant tumors, such as circulating biomarkers, cell-free DNA, and circulating tumor DNA (ctDNA). Appropriate regulatory agencies, such the Food and Drug Administration (FDA), have authorized diagnostic tests that can detect advanced tumors, forecast prognosis, and support medical professionals in therapy selection.
Market expansion is driven by increased R&D and the introduction of new technologies by key players to enhance patient screening for chronic disorders and abnormalities. Additionally, several life science companies are offering liquid biopsy testing solutions across various regions to provide targeted therapies for cancer patients.
Technological developments, rising cancer rates, and a strong emphasis on early detection and individualized medicine are driving the US industry. For instance, the American Cancer Society projects that 609,360 deaths caused by cancer and 1.9 million new cancer cases occurred in the US in 2022. The US market offers the advantages of a strong healthcare infrastructure as well as the presence of significant pharmaceutical and biotechnology businesses that are actively involved in research and development. High-profile companies such as Grail, Guardant Health, and Foundation Medicine are at the forefront of liquid biopsy innovation, contributing to the markets dynamic growth. For instance, in February 2021, Guardant Health, Inc. introduced the Guardant reveal test for patients with early-stage colorectal cancer, which measures residual disease and recurrence.
Europe is the second leading region in the market. Europe’s significant share of 29.5% is attributed to increasing awareness about cancer and prenatal screening among the population. For instance, according to data published by MDPI in 2022, approximately 6,560 patients annually benefit from liquid biopsy tests for Non-Small Cell Lung Cancer (NSCLC) screening in Europe. Moreover, numerous market players are focusing on securing funding to develop advanced liquid biopsy platforms.
The increasing occurrence of genetic abnormalities like Down syndrome and chromosomal aneuploidies is fueling market expansion in the Asia Pacific region. It is expected to show the highest compound annual growth rate (CAGR) during the study period, driven by rising demand for predictive screening due to elevated disease prevalence. For instance, as per a ScienceDirect article from December 2022, a study reported an estimated 265 annual liquid biopsies for Down syndrome (1 in 1,158) in Australia from 2016-2020.
Multi-Gene Parallel Analysis using NGS enables the analysis of multiple genes from a single sample simultaneously, offering comprehensive insights into the genetic landscape of cancer. NGS-based multi-gene analysis is driven by its unparalleled ability to detect a wide array of genetic mutations, alterations, and biomarkers with high sensitivity and specificity. For early cancer identification, prognosis, and customized treatment planning, this makes it a priceless tool. NGSs leadership in the market is being cemented by the growing demand for its reliable and extensive genetic information, which is a result of the growing popularity of precision medicine.
The importance of NGS in liquid biopsy bolstering the market due to ongoing developments in sequencing technology, which have lowered costs and increased accessibility significantly. Its widespread application in a range of healthcare settings, including smaller clinical laboratories and larger research institutes, has been made possible by these technological advancements. Furthermore, the combination of NGS with advanced bioinformatics databases and tools improves the understanding of complex genomic data and gives physicians valuable data.
NGS technology, a variety of tumor-causing mutations used to detect and potential post-treatment resistance mechanisms originating from pre-existing clones can be identified. In addition, prominent industry participants are creating new products to fulfill the rising need for diagnostics and preserve their competitive advantage through a broader range of offerings propelling market expansion. For instance, in January 2023, Agilent Technologies collaborated with Quest Diagnostics to offer Agilent Resolution ctDx FIRST, an NGS liquid biopsy test, in the U.S.
Recent advancements in liquid biopsies are leveraging new technologies in cancer screening, therapeutic selection, drug trial optimization, and recurrence monitoring. As the incidence of cancer rises and liquid biopsies become more common, major industry players are increasing their research and development (R&D) expenditures to carry out clinical studies on liquid biopsies with the goal of offering precise medication solutions. Important market participants are working together with other businesses and academic institutions to improve liquid biopsy-based treatment alternatives, which will support the markets further expansion.
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The competitive landscape of the Liquid Biopsy is dynamic and driven by technological advancements and strategic collaborations among key players. Because it is non-invasive and has the ability to detect and monitor cancer early, liquid biopsy which analyzes biomarkers like circulating tumor DNA (ctDNA) or circulating tumor cells (CTCs) from blood or other bodily fluids—is becoming more and more popular. Prominent companies like Illumina, Bio-Rad Laboratories, Roche Diagnostics, Guardant Health, and more control the market with their extensive biomarker panels and cutting-edge testing platforms.
The key players in the global Liquid Biopsy market include - Bio-Rad Laboratories among others.
The global Liquid Biopsy market can be categorized as Product & Services, Circulating Biomarkers, Clinical Applications, Technology, Application, Sample Type, End User and Region.
| Parameter | Details |
|---|---|
| Segment Covered | By Product & Services
By Circulating Biomarkers
By Clinical Applications
By Technology
By Application
By Sample Type
By End User
By Region
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| Companies Covered |
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