FIT screening

Colorectal cancer (CRC) is one of the most frequently diagnosed cancers. The good news is that CRC incidence and mortality can be reduced significantly if detected early enough.

Faecal immunochemical tests (FIT) are non-invasive and can detect blood in stool invisible to the naked eye. Due to its simplicity, FIT is currently considered the best non-invasive test for CRC screening.

Invest a little time in your own health by taking the FIT to prevent or detect colon cancer early on.
For further information, please visit our ‘FIT for screening’ website





The WPC channel was designed to further classify samples initially flagged positive for ‘Blasts/Abn Lympho?’ by the XN-DIFF channel.

The reagent reaction caused by the explicit reagents for the WPC channel depends specifically on the composition of the membrane lipids. Mature white blood cells have a membrane lipid composition different to immature or reactive cells, so they are affected to a greater extent, leaving the cells in a less native stage. This makes the membrane more permeable for the proprietary fluorescence marker that labels the cells in the second stage of the reaction. The signals corre¬sponding to cell volume and fluorescence are therefore directly related to the functionality of the cells.

Due to their membrane lipid composition, blasts are not permeated very strongly by the lysis reagent. Consequently, they show relatively low fluorescence signals and high signals for cell volume because they remain mostly intact. Neoplastic lymphocytes on the other hand are more mature and their membranes are more readily permeated, causing higher fluorescence signals and smaller volume signals due to cell shrinking. These differences allow a reliable identification of such malignant cells.

Fig. WPC channel scattergram

The added value of the WPC channel
WPC analysis excludes malignant conditions with great specificity. It minimises the number of false-positive suspected malignant samples from the XN-DIFF. This streamlines and accelerates the diagnostic pathway as it reduces the need to perform time-consuming and expensive follow-up tests that are required when a malignant condition is suspected.

The combination of XN-DIFF and WPC delivers maximum differentiation between malignant and reactive samples and deeper insight into the immune response status once malignant conditions have been excluded. The Extended Inflammation Parameters can be used with confidence.
Optionally, the WPC channel can be used to quantify haematopoietic progenitor cells.

Fluorescence flow cytometry

DC sheath flow detection method

SLS detection

WBC differential channel

RET channel

PLT-F channel

White Blood Cells

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