Application of bone marrow samples for discrimination of acute promyelocytic leukemia from other types of acute leukemia using the routine automated hematology analyzer

Summary Introduction Unreported parameters produced by automated blood cell counter, particularly large unstained cells (LUC) and delta neutrophil index (DNI), indicated the presence of immature and possibly abnormal cell populations in white blood cell population. The purpose of this study was to i...

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Veröffentlicht in:International journal of laboratory hematology 2014-10, Vol.36 (5), p.531-540
Hauptverfasser: Jang, M. J., Choi, H. W., Lee, S. Y., Lee, O. J., Kim, H. R., Shin, J. H., Suh, S. P., Ryang, D. W., Shin, M. G.
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container_issue 5
container_start_page 531
container_title International journal of laboratory hematology
container_volume 36
creator Jang, M. J.
Choi, H. W.
Lee, S. Y.
Lee, O. J.
Kim, H. R.
Shin, J. H.
Suh, S. P.
Ryang, D. W.
Shin, M. G.
description Summary Introduction Unreported parameters produced by automated blood cell counter, particularly large unstained cells (LUC) and delta neutrophil index (DNI), indicated the presence of immature and possibly abnormal cell populations in white blood cell population. The purpose of this study was to investigate the laboratory performance for discrimination of acute promyelocytic leukemia (APL) cells from other types of leukemia cells and clinical value of LUC and DNI parameters in bone marrow (BM) samples of patients with acute leukemia. Methods A total of 73 BM samples of patients with various type of acute leukemia were analyzed. LUC and DNI parameters were determined by an automated hematology analyzer (ADVIA 120; Siemens Healthcare Diagnostics, New York, NY, USA). Statistical analysis was performed using Kruskal–Wallis and Mann–Whitney U methods. Receiver operating characteristic curve (ROC) analysis, survival analysis, and Cox proportional hazard model were used to evaluate the clinical implication. Results There were significant differences (P 
doi_str_mv 10.1111/ijlh.12183
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J. ; Choi, H. W. ; Lee, S. Y. ; Lee, O. J. ; Kim, H. R. ; Shin, J. H. ; Suh, S. P. ; Ryang, D. W. ; Shin, M. G.</creator><creatorcontrib>Jang, M. J. ; Choi, H. W. ; Lee, S. Y. ; Lee, O. J. ; Kim, H. R. ; Shin, J. H. ; Suh, S. P. ; Ryang, D. W. ; Shin, M. G.</creatorcontrib><description>Summary Introduction Unreported parameters produced by automated blood cell counter, particularly large unstained cells (LUC) and delta neutrophil index (DNI), indicated the presence of immature and possibly abnormal cell populations in white blood cell population. The purpose of this study was to investigate the laboratory performance for discrimination of acute promyelocytic leukemia (APL) cells from other types of leukemia cells and clinical value of LUC and DNI parameters in bone marrow (BM) samples of patients with acute leukemia. Methods A total of 73 BM samples of patients with various type of acute leukemia were analyzed. LUC and DNI parameters were determined by an automated hematology analyzer (ADVIA 120; Siemens Healthcare Diagnostics, New York, NY, USA). Statistical analysis was performed using Kruskal–Wallis and Mann–Whitney U methods. Receiver operating characteristic curve (ROC) analysis, survival analysis, and Cox proportional hazard model were used to evaluate the clinical implication. Results There were significant differences (P &lt; 0.05) between APL group and other group in the DNI and LUC values except for DNI between APL group and non‐APL myeloid leukemia group. The area under curve of LUC was larger than that of DNI from the ROC analysis for discrimination between APL group and other group. High LUC value was associated with the increased risk of adverse outcomes and the worse overall survival in patients with acute leukemia. Conclusion Delta neutrophil index and LUC in BM showed discriminating power of APL cells from other leukemia cells.</description><identifier>ISSN: 1751-5521</identifier><identifier>EISSN: 1751-553X</identifier><identifier>DOI: 10.1111/ijlh.12183</identifier><identifier>PMID: 24410923</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>acute leukemias ; Adolescent ; Adult ; Area Under Curve ; Automated hematology analyzer ; Automation, Laboratory ; Bone Marrow - pathology ; Case-Control Studies ; Child ; Chromosomes, Human, Pair 15 ; Chromosomes, Human, Pair 17 ; delta neutrophil index ; Diagnosis, Differential ; Female ; flow cytometry ; Humans ; large unstained cell ; Leukemia, Myeloid, Acute - classification ; Leukemia, Myeloid, Acute - diagnosis ; Leukemia, Myeloid, Acute - mortality ; Leukemia, Myeloid, Acute - pathology ; Leukemia, Promyelocytic, Acute - diagnosis ; Leukemia, Promyelocytic, Acute - genetics ; Leukemia, Promyelocytic, Acute - mortality ; Leukemia, Promyelocytic, Acute - pathology ; Male ; Middle Aged ; Neutrophils - pathology ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology ; Proportional Hazards Models ; ROC Curve ; Survival Analysis ; Translocation, Genetic</subject><ispartof>International journal of laboratory hematology, 2014-10, Vol.36 (5), p.531-540</ispartof><rights>2014 John Wiley &amp; Sons Ltd</rights><rights>2014 John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5113-7384eac721cb5d90bacab7a8a45d24c67b558292698582ed757a7889f8dec0ec3</citedby><cites>FETCH-LOGICAL-c5113-7384eac721cb5d90bacab7a8a45d24c67b558292698582ed757a7889f8dec0ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fijlh.12183$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fijlh.12183$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27931,27932,45581,45582</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24410923$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jang, M. J.</creatorcontrib><creatorcontrib>Choi, H. W.</creatorcontrib><creatorcontrib>Lee, S. Y.</creatorcontrib><creatorcontrib>Lee, O. J.</creatorcontrib><creatorcontrib>Kim, H. R.</creatorcontrib><creatorcontrib>Shin, J. H.</creatorcontrib><creatorcontrib>Suh, S. P.</creatorcontrib><creatorcontrib>Ryang, D. W.</creatorcontrib><creatorcontrib>Shin, M. G.</creatorcontrib><title>Application of bone marrow samples for discrimination of acute promyelocytic leukemia from other types of acute leukemia using the routine automated hematology analyzer</title><title>International journal of laboratory hematology</title><addtitle>Int. Jnl. Lab. Hem</addtitle><description>Summary Introduction Unreported parameters produced by automated blood cell counter, particularly large unstained cells (LUC) and delta neutrophil index (DNI), indicated the presence of immature and possibly abnormal cell populations in white blood cell population. The purpose of this study was to investigate the laboratory performance for discrimination of acute promyelocytic leukemia (APL) cells from other types of leukemia cells and clinical value of LUC and DNI parameters in bone marrow (BM) samples of patients with acute leukemia. Methods A total of 73 BM samples of patients with various type of acute leukemia were analyzed. LUC and DNI parameters were determined by an automated hematology analyzer (ADVIA 120; Siemens Healthcare Diagnostics, New York, NY, USA). Statistical analysis was performed using Kruskal–Wallis and Mann–Whitney U methods. Receiver operating characteristic curve (ROC) analysis, survival analysis, and Cox proportional hazard model were used to evaluate the clinical implication. Results There were significant differences (P &lt; 0.05) between APL group and other group in the DNI and LUC values except for DNI between APL group and non‐APL myeloid leukemia group. The area under curve of LUC was larger than that of DNI from the ROC analysis for discrimination between APL group and other group. High LUC value was associated with the increased risk of adverse outcomes and the worse overall survival in patients with acute leukemia. Conclusion Delta neutrophil index and LUC in BM showed discriminating power of APL cells from other leukemia cells.</description><subject>acute leukemias</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Area Under Curve</subject><subject>Automated hematology analyzer</subject><subject>Automation, Laboratory</subject><subject>Bone Marrow - pathology</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Chromosomes, Human, Pair 15</subject><subject>Chromosomes, Human, Pair 17</subject><subject>delta neutrophil index</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>flow cytometry</subject><subject>Humans</subject><subject>large unstained cell</subject><subject>Leukemia, Myeloid, Acute - classification</subject><subject>Leukemia, Myeloid, Acute - diagnosis</subject><subject>Leukemia, Myeloid, Acute - mortality</subject><subject>Leukemia, Myeloid, Acute - pathology</subject><subject>Leukemia, Promyelocytic, Acute - diagnosis</subject><subject>Leukemia, Promyelocytic, Acute - genetics</subject><subject>Leukemia, Promyelocytic, Acute - mortality</subject><subject>Leukemia, Promyelocytic, Acute - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neutrophils - pathology</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology</subject><subject>Proportional Hazards Models</subject><subject>ROC Curve</subject><subject>Survival Analysis</subject><subject>Translocation, Genetic</subject><issn>1751-5521</issn><issn>1751-553X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1TAUhC0EoqWw4QGQlwgpxT9xnCyrQv90BRICwc5ynJNet06c2o5KeCIeE19umyV4M5b1zRwdD0KvKTmm-by3N257TBmt-RN0SKWghRD8x9P1zugBehHjDSFClqR5jg5YWVLSMH6Ifp9Mk7NGJ-tH7Hvc-hHwoEPw9zjqYXIQce8D7mw0wQ52XElt5gR4Cn5YwHmzJGuwg_kWBqtxn5-xT1sIOC1TzlgNKzJHO17jjODg52TzWD0nP-gEHd5CVu_89YL1qN3yC8JL9KzXLsKrBz1C384-fj29KDafzy9PTzaFEZTyQvK6BG0ko6YVXUNabXQrda1L0bHSVLIVomYNq5o6K3RSSC3ruunrDgwBw4_Q231u3uxuhpjUkFcH5_QIfo6KVrSmFasq9n9UVJyIRvAd-m6PmuBjDNCrKf-mDouiRO1KVLsS1d8SM_zmIXduB-hW9LG1DNA9cG8dLP-IUpdXm4vH0GLvsTHBz9Wjw62qJJdCff90rq7OvpAPbMNUw_8AMFa61w</recordid><startdate>201410</startdate><enddate>201410</enddate><creator>Jang, M. J.</creator><creator>Choi, H. W.</creator><creator>Lee, S. Y.</creator><creator>Lee, O. J.</creator><creator>Kim, H. R.</creator><creator>Shin, J. H.</creator><creator>Suh, S. P.</creator><creator>Ryang, D. W.</creator><creator>Shin, M. G.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>201410</creationdate><title>Application of bone marrow samples for discrimination of acute promyelocytic leukemia from other types of acute leukemia using the routine automated hematology analyzer</title><author>Jang, M. J. ; Choi, H. W. ; Lee, S. Y. ; Lee, O. J. ; Kim, H. R. ; Shin, J. H. ; Suh, S. P. ; Ryang, D. W. ; Shin, M. 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J.</creatorcontrib><creatorcontrib>Choi, H. W.</creatorcontrib><creatorcontrib>Lee, S. Y.</creatorcontrib><creatorcontrib>Lee, O. J.</creatorcontrib><creatorcontrib>Kim, H. R.</creatorcontrib><creatorcontrib>Shin, J. H.</creatorcontrib><creatorcontrib>Suh, S. P.</creatorcontrib><creatorcontrib>Ryang, D. W.</creatorcontrib><creatorcontrib>Shin, M. G.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>International journal of laboratory hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jang, M. J.</au><au>Choi, H. W.</au><au>Lee, S. Y.</au><au>Lee, O. J.</au><au>Kim, H. R.</au><au>Shin, J. H.</au><au>Suh, S. P.</au><au>Ryang, D. W.</au><au>Shin, M. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of bone marrow samples for discrimination of acute promyelocytic leukemia from other types of acute leukemia using the routine automated hematology analyzer</atitle><jtitle>International journal of laboratory hematology</jtitle><addtitle>Int. Jnl. Lab. Hem</addtitle><date>2014-10</date><risdate>2014</risdate><volume>36</volume><issue>5</issue><spage>531</spage><epage>540</epage><pages>531-540</pages><issn>1751-5521</issn><eissn>1751-553X</eissn><abstract>Summary Introduction Unreported parameters produced by automated blood cell counter, particularly large unstained cells (LUC) and delta neutrophil index (DNI), indicated the presence of immature and possibly abnormal cell populations in white blood cell population. The purpose of this study was to investigate the laboratory performance for discrimination of acute promyelocytic leukemia (APL) cells from other types of leukemia cells and clinical value of LUC and DNI parameters in bone marrow (BM) samples of patients with acute leukemia. Methods A total of 73 BM samples of patients with various type of acute leukemia were analyzed. LUC and DNI parameters were determined by an automated hematology analyzer (ADVIA 120; Siemens Healthcare Diagnostics, New York, NY, USA). Statistical analysis was performed using Kruskal–Wallis and Mann–Whitney U methods. Receiver operating characteristic curve (ROC) analysis, survival analysis, and Cox proportional hazard model were used to evaluate the clinical implication. Results There were significant differences (P &lt; 0.05) between APL group and other group in the DNI and LUC values except for DNI between APL group and non‐APL myeloid leukemia group. The area under curve of LUC was larger than that of DNI from the ROC analysis for discrimination between APL group and other group. High LUC value was associated with the increased risk of adverse outcomes and the worse overall survival in patients with acute leukemia. Conclusion Delta neutrophil index and LUC in BM showed discriminating power of APL cells from other leukemia cells.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24410923</pmid><doi>10.1111/ijlh.12183</doi><tpages>10</tpages></addata></record>
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subjects acute leukemias
Adolescent
Adult
Area Under Curve
Automated hematology analyzer
Automation, Laboratory
Bone Marrow - pathology
Case-Control Studies
Child
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 17
delta neutrophil index
Diagnosis, Differential
Female
flow cytometry
Humans
large unstained cell
Leukemia, Myeloid, Acute - classification
Leukemia, Myeloid, Acute - diagnosis
Leukemia, Myeloid, Acute - mortality
Leukemia, Myeloid, Acute - pathology
Leukemia, Promyelocytic, Acute - diagnosis
Leukemia, Promyelocytic, Acute - genetics
Leukemia, Promyelocytic, Acute - mortality
Leukemia, Promyelocytic, Acute - pathology
Male
Middle Aged
Neutrophils - pathology
Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis
Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality
Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology
Proportional Hazards Models
ROC Curve
Survival Analysis
Translocation, Genetic
title Application of bone marrow samples for discrimination of acute promyelocytic leukemia from other types of acute leukemia using the routine automated hematology analyzer
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