Working together for better patient care

Clinical standardization is not only helpful in preventing errors but can enable better proactive, care such as earlier diagnosis and interventions. When certain tests have been peer-reviewed and approved, standardizing with these approaches means samples will be properly prepared and results correctly interpreted.

Standardization can inhibit further discoveries, however, are new methods necessary when internationally adopted and approved assays have been shown to be accurate in diagnosing and monitoring for specific disease? After all, a patient life is on the other end.

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International clinical hematological consortium

What is the EuroFlow™ Consortium?:

        • The EuroFlow™ Consortium consists of more than 20 independent diagnostic research groups located across the world.
        • The main objective of EuroFlow™ is the development and standardization of fast, accurate, and highly sensitive flow cytometric tests for diagnosis and prognostic (sub)classification of hematological malignancies and for evaluating treatment effectiveness during follow-up.
        • The EuroFlow™ consortium has released panels for leukemia and lymphoma diagnosis, Minimal Residual Disease (MRD) analysis, and more.
        • The successful implementation of the proposal and the dissemination of the results to hematological laboratories should result in healthcare progress through more precise diagnosis and individualized treatment.
Learn more about the peer-reviewed standardized EuroFlow™ approach

The EuroFlow™ Methodology for leukemia and lymphoma diagnosis 

Getting the right flow cytometry results has an evident impact on patient care. Data processing and analysis must be fast, precise and objective to allow for correct and timely decision-making. 

Each EuroFlow™ panel represents specific antibody combinations which have been carefully selected with combinations of backbone markers and characterization markers for selecting and characterizing the cell population of interest.

The EuroFlow™ methodology represents many different panels for both screening and diagnosis of leukemia and lymphoma.


Ref: van Dongen JJM, Lhermitte L, Böttcher S, et al. on behalf of the EuroFlow™ Consortium (EU-FP6, LSHB-CT-2006-018708). EuroFlow™ antibody panels for standardized n-dimensional flow cytometric immunophenotyping of normal, reactive and malignant leukocytes. Leukemia. 2012;26(9): 1908-1975. doi: 10.1038/leu.2012.120


Interpretating results and making the right clinical decisions

Using flow cytometry results to make the right decision on a course of treatment can be difficult. Clinical data can be very complex, but with the right resources, interpreting your data can produce results with ease and simplicity.

The EuroFlow™ Consortium has developed Infinicyt™, an advanced data analysis tool to help support the EuroFlow™ panels.


What are the advantages of Infinicyt™ software?

  • The EuroFlow™ algorithms and databases use real patient samples to provide a reliable and reproducible reference tool that will help you and your team during the complex immunophenotypic reviews and numerical comparison of patient samples.
  • Database Automated Gating and Identification (AG&I) is a fully automated approach for gating and identifying the distinct cell populations present in your sample, using the Euroflow™ Database.
  • The easy-to-read Automatic Report displays all relevant results obtained during the analysis, with predefined database-specific alerts and a general conclusion without the user's input.
  • The Databases for Compass Classification compares your patient sample with abnormal references, helping with a reliable decision.


Click here to learn more about the EuroFlow™ algorithms and Database.

A complete end-to-end standardized approach for leukemia and lymphoma diagnostic. A standardized proven solution for peace of mind.

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Let's have a conversation

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With increasing sample volume combined with laboratory staff shortages, it is imperative to futureproof your lab with as much automation as you can.

When evaluating your next flow cytometry solution, make sure it has the following attributes:

  • Automated daily quality control process to help drive reproducibility and standardization
  • A fully integrated sample preparation and flow cytometer for a complete walkaway workflow

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A journey towards improving patient care

Leveraging what we know, and pushing beyond to continue clinical discoveries

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References

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