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A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia

Moreau score has been used to differentiate chronic lymphocytic leukemia (CLL) from other mature B‐cell neoplasms. However, it showed limitations in Asian patients. Therefore, we conducted a new score system replacing CD5 and CD23 with CD43 and CD180 to evaluate its diagnostic value of CLL. 237 untr...

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Autores principales: Li, Yi, Tong, Xiwen, Huang, Lifang, Li, Li, Wang, Chunyan, He, Cheng, Liu, Songya, Wang, Zhiqiong, Xiao, Min, Mao, Xia, Zhang, Donghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267114/
https://www.ncbi.nlm.nih.gov/pubmed/34061467
http://dx.doi.org/10.1002/cam4.3983
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author Li, Yi
Tong, Xiwen
Huang, Lifang
Li, Li
Wang, Chunyan
He, Cheng
Liu, Songya
Wang, Zhiqiong
Xiao, Min
Mao, Xia
Zhang, Donghua
author_facet Li, Yi
Tong, Xiwen
Huang, Lifang
Li, Li
Wang, Chunyan
He, Cheng
Liu, Songya
Wang, Zhiqiong
Xiao, Min
Mao, Xia
Zhang, Donghua
author_sort Li, Yi
collection PubMed
description Moreau score has been used to differentiate chronic lymphocytic leukemia (CLL) from other mature B‐cell neoplasms. However, it showed limitations in Asian patients. Therefore, we conducted a new score system replacing CD5 and CD23 with CD43 and CD180 to evaluate its diagnostic value of CLL. 237 untreated samples diagnosed with mature B‐cell neoplasms were collected and were randomly divided into an exploratory and a validation cohort by a 2:1 ratio. The expression of CD5, CD19, CD20, CD23, CD43, CD79b, CD180, CD200, FMC7, and surface immunoglobulin (SmIg) were analyzed among all the samples. A proposed score was developed based on the logistic regression model. The sensitivity and specificity of the proposed score were calculated by ROC curves. CD43/CD180, CD200, FMC7, and CD79b were included in our new CLL score, which showed a sensitivity of 91.8% and a specificity of 83.1%. These results were confirmed in a validation cohort with a sensitivity of 90.5% (p = 0.808) and a specificity of 79.5% (p = 0.639). In CD5 negative or CD23 negative CLL group, the new CLL score displayed improved sensitivity of 79.4% compared to Moreau score and CLLflow score (41.2% and 47.1%, respectively). In atypical CLL group, the new CLL score showed improved sensitivity of 84.2% compared to Moreau score and CLLflow score (61.4% and 64.9%, respectively). This proposed atypical CLL score helped to offer an accurate differentiation of CLL from non‐CLL together with morphological and molecular methods, particularly in Chinese patients with atypical immunophenotype.
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spelling pubmed-82671142021-07-13 A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia Li, Yi Tong, Xiwen Huang, Lifang Li, Li Wang, Chunyan He, Cheng Liu, Songya Wang, Zhiqiong Xiao, Min Mao, Xia Zhang, Donghua Cancer Med Clinical Cancer Research Moreau score has been used to differentiate chronic lymphocytic leukemia (CLL) from other mature B‐cell neoplasms. However, it showed limitations in Asian patients. Therefore, we conducted a new score system replacing CD5 and CD23 with CD43 and CD180 to evaluate its diagnostic value of CLL. 237 untreated samples diagnosed with mature B‐cell neoplasms were collected and were randomly divided into an exploratory and a validation cohort by a 2:1 ratio. The expression of CD5, CD19, CD20, CD23, CD43, CD79b, CD180, CD200, FMC7, and surface immunoglobulin (SmIg) were analyzed among all the samples. A proposed score was developed based on the logistic regression model. The sensitivity and specificity of the proposed score were calculated by ROC curves. CD43/CD180, CD200, FMC7, and CD79b were included in our new CLL score, which showed a sensitivity of 91.8% and a specificity of 83.1%. These results were confirmed in a validation cohort with a sensitivity of 90.5% (p = 0.808) and a specificity of 79.5% (p = 0.639). In CD5 negative or CD23 negative CLL group, the new CLL score displayed improved sensitivity of 79.4% compared to Moreau score and CLLflow score (41.2% and 47.1%, respectively). In atypical CLL group, the new CLL score showed improved sensitivity of 84.2% compared to Moreau score and CLLflow score (61.4% and 64.9%, respectively). This proposed atypical CLL score helped to offer an accurate differentiation of CLL from non‐CLL together with morphological and molecular methods, particularly in Chinese patients with atypical immunophenotype. John Wiley and Sons Inc. 2021-06-01 /pmc/articles/PMC8267114/ /pubmed/34061467 http://dx.doi.org/10.1002/cam4.3983 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Li, Yi
Tong, Xiwen
Huang, Lifang
Li, Li
Wang, Chunyan
He, Cheng
Liu, Songya
Wang, Zhiqiong
Xiao, Min
Mao, Xia
Zhang, Donghua
A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia
title A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia
title_full A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia
title_fullStr A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia
title_full_unstemmed A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia
title_short A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia
title_sort new score including cd43 and cd180: increased diagnostic value for atypical chronic lymphocytic leukemia
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267114/
https://www.ncbi.nlm.nih.gov/pubmed/34061467
http://dx.doi.org/10.1002/cam4.3983
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