According to the latest report by IMARC Group, titled “Minimal Residual Disease (MRD) Testing Market by Technology (Flow Cytometry, Polymerase Chain Reaction (PCR), Next Generation Sequencing (NGS), and Others), Application (Hematological Malignancy, Solid Tumors), End User (Hospitals and Speciality Clinics, Diagnostic Laboratories, Academic and Research Institutes, and Others), and Region 2025-2033,“ the global minimal residual disease (MRD) testing market size reached USD 2.3 Billion in 2024. Minimal residual disease (MRD) testing is a sophisticated diagnostic approach employed in the field of oncology. This testing method is designed to detect the presence of cancer cells that remain in the patient after treatment, at levels undetectable through standard diagnostic techniques. Utilizing highly sensitive molecular and immunological methods, such as flow cytometry, polymerase chain reaction (PCR), and next-generation sequencing (NGS), MRD testing can identify the residual disease at a cellular level. These advanced techniques provide an unparalleled precision that helps clinicians assess treatment efficacy, stratify patient risk, and decide upon subsequent treatment strategies. Some of the advantages of MRD testing include the early identification of treatment failure, allowing for timely intervention and potentially better patient outcomes.
Global Minimal Residual Disease (MRD) Testing Market Trends:
The global market is majorly driven by the increasing prevalence of cancer that is demanding advanced diagnostic methods. In line with this, the growing reliance on targeted therapies and personalized medicine is creating a fertile ground for MRD Testing. Also, substantial investments in oncological research are laying the groundwork for further refinement of this diagnostic method, thereby fueling the growth of the market. Moreover, continual technological advancements in molecular diagnostics are amplifying the test's accuracy and applicability, which in turn is stimulating the market. In addition to this, the growing pool of FDA-approved tests fortifying the clinical credibility of MRD testing is resulting in a higher adoption. Furthermore, healthcare providers are acknowledging its role in patient risk stratification, which is creating a positive market outlook. The market is further strengthened by the expansion of healthcare infrastructure in emerging economies. Some of the other factors contributing to the market include the growing public awareness about early cancer detection, the initiation of educational programs by governments and non-profits concerning cancer diagnostics, and the emergence of telehealth as a complementary pathway for discussing diagnostic results. On account of the aforementioned factors, the market is anticipated to reach a value of USD 5.5 Billion by 2033, exhibiting a CAGR of 9.7% during 2025-2033.
Market Summary:
Report Features | Details |
---|---|
Base Year of the Analysis | 2024 |
Historical Period | 2019-2024 |
Forecast Period | 2025-2033 |
Units | Billion USD |
Technologies Covered | Flow Cytometry, Polymerase Chain Reaction (PCR), Next Generation Sequencing (NGS), Others |
Applications Covered |
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End Users Covered | Hospitals and Speciality Clinics, Diagnostic Laboratories, Academic and Research Institutes, Others |
Regions Covered | Asia Pacific, Europe, North America, Latin America, Middle East and Africa |
Countries Covered | United States, Canada, Germany, France, United Kingdom, Italy, Spain, Russia, China, Japan, India, South Korea, Australia, Indonesia, Brazil, Mexico |
Companies Covered | Adaptive Biotechnologies Corporation, Arup Laboratories Inc., Bio-Rad Laboratories Inc., Guardant Health, Invivoscribe Inc., Natera Inc., NeoGenomics Laboratories Inc., Sysmex Corporation, etc. |
Customization Scope | 10% Free Customization |
Post-Sale Analyst Support | 10-12 Weeks |
Delivery Format | PDF and Excel through Email (We can also provide the editable version of the report in PPT/Word format on special request) |
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