Novel flowcytometry-based approach of malignant cell detection in body fluids using an automated hematology analyzer
Morphological microscopic examinations of nucleated cells in body fluid (BF) samples are performed to screen malignancy. However, the morphological differentiation is time-consuming and labor-intensive. This study aimed to develop a new flowcytometry-based gating analysis mode "XN-BF gating alg...
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Published in | PloS one Vol. 13; no. 2; p. e0190886 |
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Main Authors | , , , , , , , , , , |
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09.02.2018
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Abstract | Morphological microscopic examinations of nucleated cells in body fluid (BF) samples are performed to screen malignancy. However, the morphological differentiation is time-consuming and labor-intensive. This study aimed to develop a new flowcytometry-based gating analysis mode "XN-BF gating algorithm" to detect malignant cells using an automated hematology analyzer, Sysmex XN-1000. XN-BF mode was equipped with WDF white blood cell (WBC) differential channel. We added two algorithms to the WDF channel: Rule 1 detects larger and clumped cell signals compared to the leukocytes, targeting the clustered malignant cells; Rule 2 detects middle sized mononuclear cells containing less granules than neutrophils with similar fluorescence signal to monocytes, targeting hematological malignant cells and solid tumor cells. BF samples that meet, at least, one rule were detected as malignant. To evaluate this novel gating algorithm, 92 various BF samples were collected. Manual microscopic differentiation with the May-Grunwald Giemsa stain and WBC count with hemocytometer were also performed. The performance of these three methods were evaluated by comparing with the cytological diagnosis. The XN-BF gating algorithm achieved sensitivity of 63.0% and specificity of 87.8% with 68.0% for positive predictive value and 85.1% for negative predictive value in detecting malignant-cell positive samples. Manual microscopic WBC differentiation and WBC count demonstrated 70.4% and 66.7% of sensitivities, and 96.9% and 92.3% of specificities, respectively. The XN-BF gating algorithm can be a feasible tool in hematology laboratories for prompt screening of malignant cells in various BF samples. |
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AbstractList | Morphological microscopic examinations of nucleated cells in body fluid (BF) samples are performed to screen malignancy. However, the morphological differentiation is time-consuming and labor-intensive. This study aimed to develop a new flowcytometry-based gating analysis mode “XN-BF gating algorithm” to detect malignant cells using an automated hematology analyzer, Sysmex XN-1000. XN-BF mode was equipped with WDF white blood cell (WBC) differential channel. We added two algorithms to the WDF channel: Rule 1 detects larger and clumped cell signals compared to the leukocytes, targeting the clustered malignant cells; Rule 2 detects middle sized mononuclear cells containing less granules than neutrophils with similar fluorescence signal to monocytes, targeting hematological malignant cells and solid tumor cells. BF samples that meet, at least, one rule were detected as malignant. To evaluate this novel gating algorithm, 92 various BF samples were collected. Manual microscopic differentiation with the May-Grunwald Giemsa stain and WBC count with hemocytometer were also performed. The performance of these three methods were evaluated by comparing with the cytological diagnosis. The XN-BF gating algorithm achieved sensitivity of 63.0% and specificity of 87.8% with 68.0% for positive predictive value and 85.1% for negative predictive value in detecting malignant-cell positive samples. Manual microscopic WBC differentiation and WBC count demonstrated 70.4% and 66.7% of sensitivities, and 96.9% and 92.3% of specificities, respectively. The XN-BF gating algorithm can be a feasible tool in hematology laboratories for prompt screening of malignant cells in various BF samples. Morphological microscopic examinations of nucleated cells in body fluid (BF) samples are performed to screen malignancy. However, the morphological differentiation is time-consuming and labor-intensive. This study aimed to develop a new flowcytometry-based gating analysis mode "XN-BF gating algorithm" to detect malignant cells using an automated hematology analyzer, Sysmex XN-1000. XN-BF mode was equipped with WDF white blood cell (WBC) differential channel. We added two algorithms to the WDF channel: Rule 1 detects larger and clumped cell signals compared to the leukocytes, targeting the clustered malignant cells; Rule 2 detects middle sized mononuclear cells containing less granules than neutrophils with similar fluorescence signal to monocytes, targeting hematological malignant cells and solid tumor cells. BF samples that meet, at least, one rule were detected as malignant. To evaluate this novel gating algorithm, 92 various BF samples were collected. Manual microscopic differentiation with the May-Grunwald Giemsa stain and WBC count with hemocytometer were also performed. The performance of these three methods were evaluated by comparing with the cytological diagnosis. The XN-BF gating algorithm achieved sensitivity of 63.0% and specificity of 87.8% with 68.0% for positive predictive value and 85.1% for negative predictive value in detecting malignant-cell positive samples. Manual microscopic WBC differentiation and WBC count demonstrated 70.4% and 66.7% of sensitivities, and 96.9% and 92.3% of specificities, respectively. The XN-BF gating algorithm can be a feasible tool in hematology laboratories for prompt screening of malignant cells in various BF samples.Morphological microscopic examinations of nucleated cells in body fluid (BF) samples are performed to screen malignancy. However, the morphological differentiation is time-consuming and labor-intensive. This study aimed to develop a new flowcytometry-based gating analysis mode "XN-BF gating algorithm" to detect malignant cells using an automated hematology analyzer, Sysmex XN-1000. XN-BF mode was equipped with WDF white blood cell (WBC) differential channel. We added two algorithms to the WDF channel: Rule 1 detects larger and clumped cell signals compared to the leukocytes, targeting the clustered malignant cells; Rule 2 detects middle sized mononuclear cells containing less granules than neutrophils with similar fluorescence signal to monocytes, targeting hematological malignant cells and solid tumor cells. BF samples that meet, at least, one rule were detected as malignant. To evaluate this novel gating algorithm, 92 various BF samples were collected. Manual microscopic differentiation with the May-Grunwald Giemsa stain and WBC count with hemocytometer were also performed. The performance of these three methods were evaluated by comparing with the cytological diagnosis. The XN-BF gating algorithm achieved sensitivity of 63.0% and specificity of 87.8% with 68.0% for positive predictive value and 85.1% for negative predictive value in detecting malignant-cell positive samples. Manual microscopic WBC differentiation and WBC count demonstrated 70.4% and 66.7% of sensitivities, and 96.9% and 92.3% of specificities, respectively. The XN-BF gating algorithm can be a feasible tool in hematology laboratories for prompt screening of malignant cells in various BF samples. |
Author | Uchihashi, Kinya Ohsaka, Akimichi Takahashi, Toshihiro Horii, Takashi Ai, Tomohiko Kimura, Konobu Yang, Haeun Tabe, Yoko Tsuchiya, Koji Konishi, Aya Takemura, Hiroyuki |
AuthorAffiliation | 3 Department of Clinical Laboratory, Juntendo University Hospital, Tokyo, Japan 4 Sysmex, Hematology-Product Engineering, Product Development, Kobe, Japan 2 Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan 5 Department of Transfusion Medicine and Stem Cell Regulation, Juntendo University Graduate School of Medicine, Tokyo, Japan 1 Department of Next Generation Hematology Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan Universidade Nova de Lisboa Instituto de Higiene e Medicina Tropical, PORTUGAL |
AuthorAffiliation_xml | – name: 1 Department of Next Generation Hematology Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan – name: 4 Sysmex, Hematology-Product Engineering, Product Development, Kobe, Japan – name: 2 Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan – name: 3 Department of Clinical Laboratory, Juntendo University Hospital, Tokyo, Japan – name: 5 Department of Transfusion Medicine and Stem Cell Regulation, Juntendo University Graduate School of Medicine, Tokyo, Japan – name: Universidade Nova de Lisboa Instituto de Higiene e Medicina Tropical, PORTUGAL |
Author_xml | – sequence: 1 givenname: Tomohiko orcidid: 0000-0003-0376-0227 surname: Ai fullname: Ai, Tomohiko – sequence: 2 givenname: Yoko surname: Tabe fullname: Tabe, Yoko – sequence: 3 givenname: Hiroyuki surname: Takemura fullname: Takemura, Hiroyuki – sequence: 4 givenname: Konobu surname: Kimura fullname: Kimura, Konobu – sequence: 5 givenname: Toshihiro surname: Takahashi fullname: Takahashi, Toshihiro – sequence: 6 givenname: Haeun surname: Yang fullname: Yang, Haeun – sequence: 7 givenname: Koji surname: Tsuchiya fullname: Tsuchiya, Koji – sequence: 8 givenname: Aya surname: Konishi fullname: Konishi, Aya – sequence: 9 givenname: Kinya surname: Uchihashi fullname: Uchihashi, Kinya – sequence: 10 givenname: Takashi surname: Horii fullname: Horii, Takashi – sequence: 11 givenname: Akimichi surname: Ohsaka fullname: Ohsaka, Akimichi |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29425230$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_clinbiochem_2025_110888 crossref_primary_10_1055_s_0043_1776287 crossref_primary_10_1515_almed_2021_0011 crossref_primary_10_1097_MD_0000000000030611 crossref_primary_10_25207_1608_6228_2019_26_1_58_66 crossref_primary_10_1111_ijlh_13034 crossref_primary_10_1016_j_cca_2020_07_058 crossref_primary_10_1111_ijlh_13039 crossref_primary_10_1111_ijlh_13269 crossref_primary_10_3788_LOP220662 crossref_primary_10_33667_2078_5631_2023_23_40_45 crossref_primary_10_1111_ijlh_13813 crossref_primary_10_1111_ijlh_12968 crossref_primary_10_4103_IJPM_IJPM_802_18 crossref_primary_10_1515_almed_2020_0087 crossref_primary_10_3892_ol_2019_10118 crossref_primary_10_1111_ijlh_13190 |
Cites_doi | 10.1016/j.cca.2016.08.018 10.1515/cclm-2011-0927 10.1111/ijlh.12393 10.1093/ajcp/102.4.439 10.1093/ajcp/aqv093 10.1093/ajcp/70.6.855 10.1007/s10616-013-9609-8 10.1038/nri.2016.56 10.1093/carcin/18.4.739 10.5858/arpa.2013-0295-OA 10.1055/s-0030-1254048 10.1111/ijlh.12292 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Competing Interests: Department of Next Generation Hematology Laboratory Medicine at Juntendo University (Tokyo, Japan) has been financially supported by Sysmex (Kobe, Japan). This study was performed as a collaboratory project between the two institutions. Accuracy of any part of the study was appropriately investigated. The participation of these authors does not alter our adherence to PLOS ONE policies on sharing data and materials. |
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Snippet | Morphological microscopic examinations of nucleated cells in body fluid (BF) samples are performed to screen malignancy. However, the morphological... |
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SubjectTerms | Algorithms Biology and Life Sciences Body fluids Cellular biology Cerebrospinal fluid Channel gating Differentiation Flow cytometry Fluids Fluorescence Gene expression Granule cells Hematology Laboratories Leukocytes Leukocytes (mononuclear) Leukocytes (neutrophilic) Malignancy Medical diagnosis Medicine Medicine and Health Sciences Microscopy Monocytes Pathology Physical Sciences Research and Analysis Methods Sensitivity Solid tumors Stem cells Studies Tumor cells University graduates |
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Title | Novel flowcytometry-based approach of malignant cell detection in body fluids using an automated hematology analyzer |
URI | https://www.ncbi.nlm.nih.gov/pubmed/29425230 https://www.proquest.com/docview/2000040708 https://www.proquest.com/docview/2001063061 https://pubmed.ncbi.nlm.nih.gov/PMC5806859 https://doaj.org/article/8e208dd558024e71bb86cdce6b8e862a http://dx.doi.org/10.1371/journal.pone.0190886 |
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