Dublin, Jan. 22, 2026 (GLOBE NEWSWIRE) — The “Refractory Follicular Lymphoma Diagnostics Market – Global Industry Size, Share, Trends, Opportunity, and Forecast, 2021-2031” has been added to ResearchAndMarkets.com’s offering.
The Global Refractory Follicular Lymphoma Diagnostics Market is projected to expand from USD 0.49 Billion in 2025 to USD 0.69 Billion by 2031, registering a CAGR of 5.87%.
This sector comprises specialized diagnostic testing and imaging solutions designed to detect and characterize follicular lymphoma that has relapsed or failed to respond to treatment. Essential tools such as tissue biopsies, immunohistochemistry, and genomic profiling enable clinicians to confirm disease resistance and identify transformation into aggressive subtypes. Market growth is fundamentally driven by the rising global prevalence of hematologic malignancies and the increasing demand for biomarker-driven precision medicine. Data from the Leukemia & Lymphoma Society in 2024 indicates that follicular lymphoma accounted for an estimated 22% of all non-Hodgkin lymphoma diagnoses, highlighting the significant volume of patients requiring long-term disease monitoring.
Despite robust clinical demand, the market faces significant hurdles regarding the high financial burden of advanced diagnostic technologies. The elevated costs associated with molecular testing and next-generation sequencing frequently encounter reimbursement limitations, which hinders widespread accessibility and restricts market expansion in healthcare environments with limited resources.
Market Drivers
The increasing necessity for Minimal Residual Disease (MRD) monitoring is reshaping the Global Refractory Follicular Lymphoma Diagnostics Market by facilitating highly sensitive, non-invasive surveillance. Clinicians are shifting toward liquid biopsy technologies to detect circulating tumor DNA (ctDNA), permitting the identification of deep molecular remission or early relapse before clinical symptoms appear. This trend is demonstrated by the rapid adoption of next-generation sequencing assays for tracking clonal evolution; for instance, Adaptive Biotechnologies reported in their February 2025 financial results that clonoSEQ test volumes rose 35% year-over-year to 76,105 tests, reflecting the surging clinical integration of MRD assessment in lymphoid malignancies.
Furthermore, the expansion of biomarker-based precision medicine is propelling market demand, as novel bispecific antibodies require robust diagnostic profiling to guide therapeutic selection. The approval of targeted agents necessitates companion diagnostics to confirm antigen expression and monitor long-term efficacy in refractory populations. According to a December 2024 update from Genentech regarding Columvi and Lunsumio, nearly 64.0% of patients achieving a complete response to mosunetuzumab were alive without disease progression at 45 months, emphasizing the need for durable monitoring strategies. Additionally, improved therapeutic outcomes extend the testing window; OncologyNewsCentral reported in 2025 that the combination of tafasitamab, lenalidomide, and rituximab demonstrated a median progression-free survival of 22.4 months, significantly broadening the timeframe for longitudinal diagnostic oversight.
Market Challenges
The growth of the Global Refractory Follicular Lymphoma Diagnostics Market is significantly hampered by the substantial financial burden associated with deploying advanced diagnostic technologies. Specialized tools such as next-generation sequencing and molecular profiling incur high operational costs that frequently exceed the coverage limits of standard reimbursement policies. Consequently, healthcare providers in cost-sensitive environments often face administrative resistance when ordering these premium tests, forcing them to rely on less expensive but less comprehensive alternatives. This economic barrier limits the widespread adoption of precision diagnostics, thereby reducing the volume of tests performed and directly constraining revenue opportunities for market players.
This challenge is further exacerbated by the intense economic pressure within the hematologic oncology sector. Research findings from the Leukemia & Lymphoma Society in 2024 indicated that privately insured patients diagnosed with lymphoma can incur total healthcare costs exceeding $130,000 within just the first six months of care. Such elevated baseline expenditures compel healthcare systems and payers to scrutinize all ancillary costs, often resulting in the rejection or limitation of claims for high-value diagnostic procedures. This financial toxicity effectively shrinks the addressable market by rendering advanced testing solutions inaccessible to a significant portion of the patient population.
Market Trends
The Integration of Artificial Intelligence in Diagnostic Workflows is enhancing the precision and efficiency of characterizing refractory follicular lymphoma. Laboratories are increasingly transitioning beyond traditional manual reviews by adopting open digital pathology ecosystems that incorporate third-party algorithms for automated image analysis and sub-typing. This technological shift manages the increasing complexity of tissue evaluation, allowing pathologists to seamlessly deploy varied computational tools within a single interface to reduce diagnostic variability. As noted by Roche in September 2024 regarding their advancement of AI-driven cancer diagnostics, the company integrated more than 20 advanced artificial intelligence algorithms from eight new collaborators into its digital pathology software, significantly broadening the analytical capabilities available to clinicians for cancer research and diagnosis.
Concurrently, the Convergence of Multi-Omics Data for Precision Stratification is emerging as a vital trend to address the heterogeneity of disease progression in high-risk patients. Diagnostic developers are increasingly partnering with research institutions to generate comprehensive datasets that combine clinical history with genomic sequencing, proteomics, and methylation profiling. This holistic approach aims to uncover novel biomarkers that can predict early relapse more accurately than single-analyte tests, facilitating earlier intervention for aggressive transformations. According to Investing.com in November 2024, a partnership between Tempus and IFLI focuses on this multi-modal analysis to address the critical unmet need where about 20% of follicular lymphoma patients experience progressive disease within two years of initial chemoimmunotherapy.
Key Players Profiled in the Refractory Follicular Lymphoma Diagnostics Market
- Roche Diagnostics
- Abbott
- Thermo Fisher Scientific
- Agilent Technologies
- QIAGEN
- Bio-Rad
- Danaher
- Illumina
- PerkinElmer
- Cell Signaling Technology
Report Scope
In this report, the Global Refractory Follicular Lymphoma Diagnostics Market has been segmented into the following categories:
Refractory Follicular Lymphoma Diagnostics Market, by Product:
- Instruments
- Kits & Consumables
Refractory Follicular Lymphoma Diagnostics Market, by Method:
- Immunohistochemistry (IHC)
- In Situ Hybridization (ISH)
- Polymerase Chain Reaction (PCR)
- Others
Refractory Follicular Lymphoma Diagnostics Market, by End User:
- Hospitals
- Diagnostic Centers
- Others
Refractory Follicular Lymphoma Diagnostics Market, by Region:
- North America
- Europe
- Asia-Pacific
- South America
- Middle East & Africa
Key Attributes:
| Report Attribute | Details |
| No. of Pages | 180 |
| Forecast Period | 2025 – 2031 |
| Estimated Market Value (USD) in 2025 | $0.49 Billion |
| Forecasted Market Value (USD) by 2031 | $0.69 Billion |
| Compound Annual Growth Rate | 5.8% |
| Regions Covered | Global |
For more information about this report visit https://www.researchandmarkets.com/r/th756w
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- Refractory Follicular Lymphoma Diagnostics Market
