As per Intent Market Research, the Non-Invasive Cancer Diagnostics Market was valued at USD 5.3 billion in 2024-e and will surpass USD 9.6 billion by 2030; growing at a CAGR of 10.3% during 2025 - 2030.
The non-invasive cancer diagnostics market is experiencing significant growth due to the increasing demand for early detection methods and advancements in diagnostic technologies. Non-invasive cancer diagnostics, including liquid biopsy and imaging technologies, offer an alternative to traditional biopsy procedures by allowing for cancer detection through bodily fluids or advanced imaging techniques. These methods are gaining popularity due to their ability to provide early-stage detection, reduce patient discomfort, and improve overall diagnostic accuracy. The rising prevalence of cancer globally, along with growing awareness of the importance of early detection, is fueling the demand for non-invasive cancer diagnostic solutions.
Technological advancements are accelerating the market’s expansion, particularly in the development of more sensitive and accurate liquid biopsy techniques that can detect genetic mutations, tumor DNA, and other biomarkers. The market is expected to continue growing, driven by increasing investments in research and the need for personalized cancer treatments. Non-invasive diagnostics hold great promise for revolutionizing cancer care, offering less invasive options for monitoring disease progression and improving patient outcomes.
Liquid Biopsy Technology is Largest Owing to Its Potential for Early Cancer Detection
Liquid biopsy is the largest technology segment in the non-invasive cancer diagnostics market, owing to its ability to detect cancer in its early stages through the analysis of blood, urine, or other bodily fluids. This method is particularly effective in identifying genetic mutations, tumor markers, and circulating tumor DNA, which are critical in diagnosing and monitoring various types of cancer. Liquid biopsy offers several advantages over traditional biopsy methods, including the ability to assess multiple biomarkers simultaneously and the potential for repeated testing, allowing for continuous monitoring of the disease.
Liquid biopsy is also being explored for its application in detecting minimal residual disease (MRD), a crucial factor in preventing relapse in cancer patients. As the technology matures and becomes more widely available, liquid biopsy is poised to become a standard practice in oncology, particularly in early cancer detection and treatment monitoring. The growing interest in liquid biopsy, combined with advancements in genetic sequencing and biomarker identification, makes it the largest and most promising technology in the market.
Early Cancer Detection Application is Fastest Growing Owing to Demand for Early Diagnosis
Early cancer detection is the fastest growing application in the non-invasive cancer diagnostics market, driven by the increasing emphasis on diagnosing cancer in its earliest stages to improve treatment outcomes. Early-stage cancers are often asymptomatic, making them difficult to detect through conventional methods. Non-invasive technologies, such as liquid biopsy and advanced imaging techniques, offer a way to detect cancer before it progresses to later stages, increasing the chances of successful treatment and survival.
As awareness of the importance of early cancer detection grows, healthcare providers and patients alike are seeking out non-invasive diagnostic options that provide a quicker, more accurate diagnosis with minimal patient discomfort. This increasing demand for early detection is further supported by government initiatives, research funding, and the growing focus on precision medicine, which are all contributing to the rapid growth of the early cancer detection segment.
Hospitals and Diagnostic Centers End-User Segment is Largest Owing to Widespread Adoption of Non-Invasive Diagnostics
Hospitals and diagnostic centers represent the largest end-user segment in the non-invasive cancer diagnostics market. These healthcare facilities are increasingly adopting non-invasive diagnostic methods, such as liquid biopsy and imaging technologies, to detect and monitor cancer more effectively. Hospitals and diagnostic centers play a central role in the cancer diagnostic process, offering a range of services from initial screening to post-treatment monitoring. The ability to provide faster, more accurate, and less invasive diagnostic options is a key factor driving the adoption of non-invasive techniques in these settings.
The large number of cancer patients, along with the growing availability of non-invasive diagnostic tools, is contributing to the growth of this segment. As healthcare systems globally continue to prioritize early diagnosis and personalized treatment approaches, hospitals and diagnostic centers are expected to remain the largest end-users of non-invasive cancer diagnostics, particularly as these technologies become more integrated into routine cancer care.
North America is Largest Region Owing to Advanced Healthcare Infrastructure and Technological Adoption
North America is the largest region in the non-invasive cancer diagnostics market, driven by its advanced healthcare infrastructure, high rates of cancer prevalence, and rapid adoption of innovative technologies. The United States, in particular, has seen significant investments in cancer research and diagnostics, with many healthcare providers incorporating non-invasive diagnostic methods like liquid biopsy into their oncology practices. Regulatory approval for liquid biopsy tests, along with increasing reimbursement coverage, has contributed to the widespread adoption of these technologies in clinical settings.
Additionally, the growing emphasis on personalized medicine and precision oncology has bolstered the demand for non-invasive diagnostic solutions, as they allow for more accurate and tailored treatment plans. The region's robust healthcare system, coupled with its commitment to research and technological advancements, ensures that North America remains the largest market for non-invasive cancer diagnostics, with continued growth expected as technologies evolve.
Competitive Landscape
The non-invasive cancer diagnostics market is competitive, with key players including Guardant Health, Foundation Medicine, Exact Sciences, and Biocept. These companies are at the forefront of developing and commercializing liquid biopsy tests and other non-invasive diagnostic solutions for cancer. Their focus is on improving the sensitivity and accuracy of diagnostic tests, expanding their product portfolios, and gaining regulatory approvals to expand their market reach.
As the demand for early cancer detection and personalized treatment grows, these companies are investing heavily in research and development to introduce innovative products. Additionally, partnerships between diagnostic companies and healthcare providers are becoming more common to accelerate the adoption of non-invasive diagnostic technologies in clinical practice. The competitive landscape is characterized by rapid technological advancements, strategic mergers and acquisitions, and a strong focus on addressing unmet needs in cancer diagnostics.
Recent Developments:
- In December 2024, Guardant Health launched a new liquid biopsy test for early detection of colorectal cancer.
- In November 2024, Roche Diagnostics announced the FDA approval of a new blood-based test for lung cancer detection.
- In October 2024, Thermo Fisher Scientific expanded its liquid biopsy technology to include early-stage breast cancer detection.
- In September 2024, Illumina acquired a liquid biopsy startup to enhance its non-invasive cancer diagnostic offerings.
- In August 2024, Bio-Rad Laboratories introduced an exosomal RNA profiling kit for non-invasive detection of ovarian cancer.
List of Leading Companies:
- Guardant Health
- Roche Diagnostics
- Bio-Rad Laboratories
- Thermo Fisher Scientific
- Illumina
- Abbott Laboratories
- Siemens Healthineers
- Exact Sciences
- LabCorp
- Foundation Medicine
- Qiagen
- Helomics
- Freenome
- NeoGenomics
- Sysmex Corporation
Report Scope:
Report Features |
Description |
Market Size (2024-e) |
USD 5.3 billion |
Forecasted Value (2030) |
USD 9.6 billion |
CAGR (2025 – 2030) |
10.3% |
Base Year for Estimation |
2024-e |
Historic Year |
2023 |
Forecast Period |
2025 – 2030 |
Report Coverage |
Market Forecast, Market Dynamics, Competitive Landscape, Recent Developments |
Segments Covered |
Non-Invasive Cancer Diagnostics Market By Technology Type (Liquid Biopsy, Imaging Technologies), By Application (Early Cancer Detection, Monitoring Disease Progression), By End-User (Hospitals and Diagnostic Centers, Research and Clinical Laboratories, Home Care Providers) |
Regional Analysis |
North America (US, Canada, Mexico), Europe (Germany, France, UK, Italy, Spain, and Rest of Europe), Asia-Pacific (China, Japan, South Korea, Australia, India, and Rest of Asia-Pacific), Latin America (Brazil, Argentina, and Rest of Latin America), Middle East & Africa (Saudi Arabia, UAE, Rest of Middle East & Africa) |
Major Companies |
Guardant Health, Roche Diagnostics, Bio-Rad Laboratories, Thermo Fisher Scientific, Illumina, Abbott Laboratories, Siemens Healthineers, Exact Sciences, LabCorp, Foundation Medicine, Qiagen, Helomics, Freenome, NeoGenomics, Sysmex Corporation |
Customization Scope |
Customization for segments, region/country-level will be provided. Moreover, additional customization can be done based on the requirements |
1. Introduction |
1.1. Market Definition |
1.2. Scope of the Study |
1.3. Research Assumptions |
1.4. Study Limitations |
2. Research Methodology |
2.1. Research Approach |
2.1.1. Top-Down Method |
2.1.2. Bottom-Up Method |
2.1.3. Factor Impact Analysis |
2.2. Insights & Data Collection Process |
2.2.1. Secondary Research |
2.2.2. Primary Research |
2.3. Data Mining Process |
2.3.1. Data Analysis |
2.3.2. Data Validation and Revalidation |
2.3.3. Data Triangulation |
3. Executive Summary |
3.1. Major Markets & Segments |
3.2. Highest Growing Regions and Respective Countries |
3.3. Impact of Growth Drivers & Inhibitors |
3.4. Regulatory Overview by Country |
4. Non-Invasive Cancer Diagnostics Market, by Technology Type (Market Size & Forecast: USD Million, 2023 – 2030) |
4.1. Liquid Biopsy |
4.1.1. ctDNA Testing |
4.1.2. Circulating Tumor Cell (CTC) Testing |
4.1.3. Exosomal RNA Profiling |
4.2. Imaging Technologies |
4.2.1. MRI-based Detection |
4.2.2. Ultrasound-based Detection |
4.2.3. PET Scanning |
5. Non-Invasive Cancer Diagnostics Market, by Application (Market Size & Forecast: USD Million, 2023 – 2030) |
5.1. Early Cancer Detection |
5.1.1. Breast Cancer Detection |
5.1.2. Lung Cancer Detection |
5.1.3. Colorectal Cancer Detection |
5.2. Monitoring Disease Progression |
5.2.1. Detecting Metastasis |
5.2.2. Monitoring Recurrence |
6. Non-Invasive Cancer Diagnostics Market, by End-User (Market Size & Forecast: USD Million, 2023 – 2030) |
6.1. Hospitals and Diagnostic Centers |
6.2. Research and Clinical Laboratories |
6.3. Home Care Providers |
7. Regional Analysis (Market Size & Forecast: USD Million, 2023 – 2030) |
7.1. Regional Overview |
7.2. North America |
7.2.1. Regional Trends & Growth Drivers |
7.2.2. Barriers & Challenges |
7.2.3. Opportunities |
7.2.4. Factor Impact Analysis |
7.2.5. Technology Trends |
7.2.6. North America Non-Invasive Cancer Diagnostics Market, by Technology Type |
7.2.7. North America Non-Invasive Cancer Diagnostics Market, by Application |
7.2.8. North America Non-Invasive Cancer Diagnostics Market, by End-User |
7.2.9. By Country |
7.2.9.1. US |
7.2.9.1.1. US Non-Invasive Cancer Diagnostics Market, by Technology Type |
7.2.9.1.2. US Non-Invasive Cancer Diagnostics Market, by Application |
7.2.9.1.3. US Non-Invasive Cancer Diagnostics Market, by End-User |
7.2.9.2. Canada |
7.2.9.3. Mexico |
*Similar segmentation will be provided for each region and country |
7.3. Europe |
7.4. Asia-Pacific |
7.5. Latin America |
7.6. Middle East & Africa |
8. Competitive Landscape |
8.1. Overview of the Key Players |
8.2. Competitive Ecosystem |
8.2.1. Level of Fragmentation |
8.2.2. Market Consolidation |
8.2.3. Product Innovation |
8.3. Company Share Analysis |
8.4. Company Benchmarking Matrix |
8.4.1. Strategic Overview |
8.4.2. Product Innovations |
8.5. Start-up Ecosystem |
8.6. Strategic Competitive Insights/ Customer Imperatives |
8.7. ESG Matrix/ Sustainability Matrix |
8.8. Manufacturing Network |
8.8.1. Locations |
8.8.2. Supply Chain and Logistics |
8.8.3. Product Flexibility/Customization |
8.8.4. Digital Transformation and Connectivity |
8.8.5. Environmental and Regulatory Compliance |
8.9. Technology Readiness Level Matrix |
8.10. Technology Maturity Curve |
8.11. Buying Criteria |
9. Company Profiles |
9.1. Guardant Health |
9.1.1. Company Overview |
9.1.2. Company Financials |
9.1.3. Product/Service Portfolio |
9.1.4. Recent Developments |
9.1.5. IMR Analysis |
*Similar information will be provided for other companies |
9.2. Roche Diagnostics |
9.3. Bio-Rad Laboratories |
9.4. Thermo Fisher Scientific |
9.5. Illumina |
9.6. Abbott Laboratories |
9.7. Siemens Healthineers |
9.8. Exact Sciences |
9.9. LabCorp |
9.10. Foundation Medicine |
9.11. Qiagen |
9.12. Helomics |
9.13. Freenome |
9.14. NeoGenomics |
9.15. Sysmex Corporation |
10. Appendix |
A comprehensive market research approach was employed to gather and analyze data on the Non-Invasive Cancer Diagnostics Market. In the process, the analysis was also done to analyze the parent market and relevant adjacencies to measure the impact of them on the Non-Invasive Cancer Diagnostics Market. The research methodology encompassed both secondary and primary research techniques, ensuring the accuracy and credibility of the findings.
Secondary Research
Secondary research involved a thorough review of pertinent industry reports, journals, articles, and publications. Additionally, annual reports, press releases, and investor presentations of industry players were scrutinized to gain insights into their market positioning and strategies.
Primary Research
Primary research involved conducting in-depth interviews with industry experts, stakeholders, and market participants across the E-Waste Management ecosystem. The primary research objectives included:
- Validating findings and assumptions derived from secondary research
- Gathering qualitative and quantitative data on market trends, drivers, and challenges
- Understanding the demand-side dynamics, encompassing end-users, component manufacturers, facility providers, and service providers
- Assessing the supply-side landscape, including technological advancements and recent developments
Market Size Assessment
A combination of top-down and bottom-up approaches was utilized to analyze the overall size of the Non-Invasive Cancer Diagnostics Market. These methods were also employed to assess the size of various subsegments within the market. The market size assessment methodology encompassed the following steps:
- Identification of key industry players and relevant revenues through extensive secondary research
- Determination of the industry's supply chain and market size, in terms of value, through primary and secondary research processes
- Calculation of percentage shares, splits, and breakdowns using secondary sources and verification through primary sources
Data Triangulation
To ensure the accuracy and reliability of the market size, data triangulation was implemented. This involved cross-referencing data from various sources, including demand and supply side factors, market trends, and expert opinions. Additionally, top-down and bottom-up approaches were employed to validate the market size assessment.
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