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The integration of Sysmex XN‐9100’ WPC channel reflex testing in the detection of reactive versus malignant blood samples
Introduction Sysmex XN‐9100™ (Sysmex, Kobe, Japan) system has an optional White Progenitor Cell (WPC) channel. While the White Differentiation (WDF) channel reports a combined flag for blasts/abnormal lymphocytes, WPC channel specifies flagging into a separate flag for each cell type or removes the...
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Published in: | International journal of laboratory hematology 2021-04, Vol.43 (2), p.191-198 |
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container_title | International journal of laboratory hematology |
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creator | Blomme, Siska Boeckx, Nancy Brusselmans, Caroline Claerhout, Helena Van Laer, Christine |
description | Introduction
Sysmex XN‐9100™ (Sysmex, Kobe, Japan) system has an optional White Progenitor Cell (WPC) channel. While the White Differentiation (WDF) channel reports a combined flag for blasts/abnormal lymphocytes, WPC channel specifies flagging into a separate flag for each cell type or removes the flag entirely. Aim of this study was to evaluate the added value of this WPC channel in the detection of malignant samples.
Methods
Routine blood samples analyzed on Sysmex XE‐5000 with flagging for either blasts, abnormal lymphocytes, or atypical lymphocytes (n = 630) were selected for testing on Sysmex XN‐9100, resulting in a reflex WPC analysis in 420 samples. All samples were microscopically evaluated with DI‐60 digital cell imaging analyzer.
Results
WPC reflex testing resulted in a suspect flag ("blasts" and/or "abnormal lymphocytes") in 334 samples, which was confirmed microscopically in 38% (128/334). In all true positive samples, WPC correctly classified the initial WDF flag in either "blasts" flag or "abnormal lymphocytes?" flag in 75%. Only 12% (50/420) of WDF "blasts/abnormal lymphocytes" positive samples became negative after WPC reflex testing. Subgroup analysis showed differences between the "pediatric" versus "adult" groups and the "hematological/chemotherapy" versus "nonhematological/nonchemotherapy" groups in specificity and smear reduction.
Conclusion
Overall, WPC reflex testing showed good sensitivity (99%); however, the specificity remains poor (29%). Using reflex WPC to the WDF channel resulted in a 12% reduction of the smear review rate. Although the WPC channel offers different interesting advantages, additional topics and a specific workflow should be applied to optimize the use of this channel. |
doi_str_mv | 10.1111/ijlh.13352 |
format | article |
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Sysmex XN‐9100™ (Sysmex, Kobe, Japan) system has an optional White Progenitor Cell (WPC) channel. While the White Differentiation (WDF) channel reports a combined flag for blasts/abnormal lymphocytes, WPC channel specifies flagging into a separate flag for each cell type or removes the flag entirely. Aim of this study was to evaluate the added value of this WPC channel in the detection of malignant samples.
Methods
Routine blood samples analyzed on Sysmex XE‐5000 with flagging for either blasts, abnormal lymphocytes, or atypical lymphocytes (n = 630) were selected for testing on Sysmex XN‐9100, resulting in a reflex WPC analysis in 420 samples. All samples were microscopically evaluated with DI‐60 digital cell imaging analyzer.
Results
WPC reflex testing resulted in a suspect flag ("blasts" and/or "abnormal lymphocytes") in 334 samples, which was confirmed microscopically in 38% (128/334). In all true positive samples, WPC correctly classified the initial WDF flag in either "blasts" flag or "abnormal lymphocytes?" flag in 75%. Only 12% (50/420) of WDF "blasts/abnormal lymphocytes" positive samples became negative after WPC reflex testing. Subgroup analysis showed differences between the "pediatric" versus "adult" groups and the "hematological/chemotherapy" versus "nonhematological/nonchemotherapy" groups in specificity and smear reduction.
Conclusion
Overall, WPC reflex testing showed good sensitivity (99%); however, the specificity remains poor (29%). Using reflex WPC to the WDF channel resulted in a 12% reduction of the smear review rate. Although the WPC channel offers different interesting advantages, additional topics and a specific workflow should be applied to optimize the use of this channel.</description><identifier>ISSN: 1751-5521</identifier><identifier>EISSN: 1751-553X</identifier><identifier>DOI: 10.1111/ijlh.13352</identifier><identifier>PMID: 33001578</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Cell differentiation ; Chemotherapy ; hematology analyzer ; Lymphocytes ; Progenitor cells ; Sensitivity analysis ; Sysmex ; WDF channel ; WPC channel ; XN‐20</subject><ispartof>International journal of laboratory hematology, 2021-04, Vol.43 (2), p.191-198</ispartof><rights>2020 John Wiley & Sons Ltd</rights><rights>2020 John Wiley & Sons Ltd.</rights><rights>Copyright © 2021 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3932-88ef70964048b6b2593d2bb7e390d7deba9d18d845299014a3cfba66fa7dddbb3</citedby><cites>FETCH-LOGICAL-c3932-88ef70964048b6b2593d2bb7e390d7deba9d18d845299014a3cfba66fa7dddbb3</cites><orcidid>0000-0002-6128-2027 ; 0000-0002-3105-6117</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33001578$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blomme, Siska</creatorcontrib><creatorcontrib>Boeckx, Nancy</creatorcontrib><creatorcontrib>Brusselmans, Caroline</creatorcontrib><creatorcontrib>Claerhout, Helena</creatorcontrib><creatorcontrib>Van Laer, Christine</creatorcontrib><title>The integration of Sysmex XN‐9100’ WPC channel reflex testing in the detection of reactive versus malignant blood samples</title><title>International journal of laboratory hematology</title><addtitle>Int J Lab Hematol</addtitle><description>Introduction
Sysmex XN‐9100™ (Sysmex, Kobe, Japan) system has an optional White Progenitor Cell (WPC) channel. While the White Differentiation (WDF) channel reports a combined flag for blasts/abnormal lymphocytes, WPC channel specifies flagging into a separate flag for each cell type or removes the flag entirely. Aim of this study was to evaluate the added value of this WPC channel in the detection of malignant samples.
Methods
Routine blood samples analyzed on Sysmex XE‐5000 with flagging for either blasts, abnormal lymphocytes, or atypical lymphocytes (n = 630) were selected for testing on Sysmex XN‐9100, resulting in a reflex WPC analysis in 420 samples. All samples were microscopically evaluated with DI‐60 digital cell imaging analyzer.
Results
WPC reflex testing resulted in a suspect flag ("blasts" and/or "abnormal lymphocytes") in 334 samples, which was confirmed microscopically in 38% (128/334). In all true positive samples, WPC correctly classified the initial WDF flag in either "blasts" flag or "abnormal lymphocytes?" flag in 75%. Only 12% (50/420) of WDF "blasts/abnormal lymphocytes" positive samples became negative after WPC reflex testing. Subgroup analysis showed differences between the "pediatric" versus "adult" groups and the "hematological/chemotherapy" versus "nonhematological/nonchemotherapy" groups in specificity and smear reduction.
Conclusion
Overall, WPC reflex testing showed good sensitivity (99%); however, the specificity remains poor (29%). Using reflex WPC to the WDF channel resulted in a 12% reduction of the smear review rate. Although the WPC channel offers different interesting advantages, additional topics and a specific workflow should be applied to optimize the use of this channel.</description><subject>Cell differentiation</subject><subject>Chemotherapy</subject><subject>hematology analyzer</subject><subject>Lymphocytes</subject><subject>Progenitor cells</subject><subject>Sensitivity analysis</subject><subject>Sysmex</subject><subject>WDF channel</subject><subject>WPC channel</subject><subject>XN‐20</subject><issn>1751-5521</issn><issn>1751-553X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kc1uEzEQx60K1C-48ADIEheElNaf8fqIIqBFEUWiiN4sez2bbOT1Bnu3bQ6V-ghceb0-CS5pe-DAXDySf_PTaP4IvaLkiJY6bldheUQ5l2wH7VMl6URKfvHsqWd0Dx3kvCJEKkH0LtrjnBAqVbWPbs6XgNs4wCLZoe0j7hv8bZM7uMYXX-5uf2lKyN3tb_zj6wzXSxsjBJygCeV_gDy0cVGm8VAkHgaoHxUJbOkvAV9CymPGnQ3tIto4YBf63uNsu3WA_AI9b2zI8PLhPUTfP344n51M5mefTmfv55Oaa84mVQWNInoqiKjc1DGpuWfOKeCaeOXBWe1p5SshmdaECsvrxtnptLHKe-8cP0Rvt9516n-OZW_TtbmGEGyEfsyGCaGqchqhCvrmH3TVjymW7QyTRDMuGKeFerel6tTnXA5i1qntbNoYSsx9KOY-FPM3lAK_flCOrgP_hD6mUAC6Ba7aAJv_qMzp5_nJVvoHRe2ZNA</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Blomme, Siska</creator><creator>Boeckx, Nancy</creator><creator>Brusselmans, Caroline</creator><creator>Claerhout, Helena</creator><creator>Van Laer, Christine</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6128-2027</orcidid><orcidid>https://orcid.org/0000-0002-3105-6117</orcidid></search><sort><creationdate>202104</creationdate><title>The integration of Sysmex XN‐9100’ WPC channel reflex testing in the detection of reactive versus malignant blood samples</title><author>Blomme, Siska ; Boeckx, Nancy ; Brusselmans, Caroline ; Claerhout, Helena ; Van Laer, Christine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3932-88ef70964048b6b2593d2bb7e390d7deba9d18d845299014a3cfba66fa7dddbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cell differentiation</topic><topic>Chemotherapy</topic><topic>hematology analyzer</topic><topic>Lymphocytes</topic><topic>Progenitor cells</topic><topic>Sensitivity analysis</topic><topic>Sysmex</topic><topic>WDF channel</topic><topic>WPC channel</topic><topic>XN‐20</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blomme, Siska</creatorcontrib><creatorcontrib>Boeckx, Nancy</creatorcontrib><creatorcontrib>Brusselmans, Caroline</creatorcontrib><creatorcontrib>Claerhout, Helena</creatorcontrib><creatorcontrib>Van Laer, Christine</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of laboratory hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blomme, Siska</au><au>Boeckx, Nancy</au><au>Brusselmans, Caroline</au><au>Claerhout, Helena</au><au>Van Laer, Christine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The integration of Sysmex XN‐9100’ WPC channel reflex testing in the detection of reactive versus malignant blood samples</atitle><jtitle>International journal of laboratory hematology</jtitle><addtitle>Int J Lab Hematol</addtitle><date>2021-04</date><risdate>2021</risdate><volume>43</volume><issue>2</issue><spage>191</spage><epage>198</epage><pages>191-198</pages><issn>1751-5521</issn><eissn>1751-553X</eissn><abstract>Introduction
Sysmex XN‐9100™ (Sysmex, Kobe, Japan) system has an optional White Progenitor Cell (WPC) channel. While the White Differentiation (WDF) channel reports a combined flag for blasts/abnormal lymphocytes, WPC channel specifies flagging into a separate flag for each cell type or removes the flag entirely. Aim of this study was to evaluate the added value of this WPC channel in the detection of malignant samples.
Methods
Routine blood samples analyzed on Sysmex XE‐5000 with flagging for either blasts, abnormal lymphocytes, or atypical lymphocytes (n = 630) were selected for testing on Sysmex XN‐9100, resulting in a reflex WPC analysis in 420 samples. All samples were microscopically evaluated with DI‐60 digital cell imaging analyzer.
Results
WPC reflex testing resulted in a suspect flag ("blasts" and/or "abnormal lymphocytes") in 334 samples, which was confirmed microscopically in 38% (128/334). In all true positive samples, WPC correctly classified the initial WDF flag in either "blasts" flag or "abnormal lymphocytes?" flag in 75%. Only 12% (50/420) of WDF "blasts/abnormal lymphocytes" positive samples became negative after WPC reflex testing. Subgroup analysis showed differences between the "pediatric" versus "adult" groups and the "hematological/chemotherapy" versus "nonhematological/nonchemotherapy" groups in specificity and smear reduction.
Conclusion
Overall, WPC reflex testing showed good sensitivity (99%); however, the specificity remains poor (29%). Using reflex WPC to the WDF channel resulted in a 12% reduction of the smear review rate. Although the WPC channel offers different interesting advantages, additional topics and a specific workflow should be applied to optimize the use of this channel.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33001578</pmid><doi>10.1111/ijlh.13352</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-6128-2027</orcidid><orcidid>https://orcid.org/0000-0002-3105-6117</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cell differentiation Chemotherapy hematology analyzer Lymphocytes Progenitor cells Sensitivity analysis Sysmex WDF channel WPC channel XN‐20 |
title | The integration of Sysmex XN‐9100’ WPC channel reflex testing in the detection of reactive versus malignant blood samples |
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