Concordance of two approaches in monitoring of minimal residual disease in B-precursor acute lymphoblastic leukemia: Fusion transcripts and leukemia-associated immunophenotypes

Real-time quantitative polymerase chain reaction (RQ-PCR) for fusion transcripts and flow cytometry for leukemia-specific markers are widely used for minimal residual disease (MRD) detection in acute lymphoblastic leukemia, but the relation between the results of either method is unclear. Methods: M...

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Main Authors: Ying-Jung Huang, Elaine Coustan-Smith, Hsiao-Wen Kao, Hsi-Che Liu, Shih-Hsiang Chen, Chih-Cheng Hsiao, Chao-Ping Yang, Tang-Her Jaing, Ting-Chi Yeh, Ming-Chung Kuo, Chang-Liang Lai, Chia-Hui Chang, Dario Campana, Der-Cherng Liang, Lee-Yung Shih
Format: Article
Language:English
Published: Elsevier 2017-10-01
Series:Journal of the Formosan Medical Association
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0929664616304806
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author Ying-Jung Huang
Elaine Coustan-Smith
Hsiao-Wen Kao
Hsi-Che Liu
Shih-Hsiang Chen
Chih-Cheng Hsiao
Chao-Ping Yang
Tang-Her Jaing
Ting-Chi Yeh
Ming-Chung Kuo
Chang-Liang Lai
Chia-Hui Chang
Dario Campana
Der-Cherng Liang
Lee-Yung Shih
author_facet Ying-Jung Huang
Elaine Coustan-Smith
Hsiao-Wen Kao
Hsi-Che Liu
Shih-Hsiang Chen
Chih-Cheng Hsiao
Chao-Ping Yang
Tang-Her Jaing
Ting-Chi Yeh
Ming-Chung Kuo
Chang-Liang Lai
Chia-Hui Chang
Dario Campana
Der-Cherng Liang
Lee-Yung Shih
author_sort Ying-Jung Huang
collection DOAJ
description Real-time quantitative polymerase chain reaction (RQ-PCR) for fusion transcripts and flow cytometry for leukemia-specific markers are widely used for minimal residual disease (MRD) detection in acute lymphoblastic leukemia, but the relation between the results of either method is unclear. Methods: Mononucleated cells from 108 bone marrow samples collected from 55 B-precursor acute lymphoblastic leukemia patients (30 with t(12;21)/ETV6-RUNX1, 16 with t(9;22)/BCR-ABL1 and nine with t(1;19)/TCF3-PBX1) were examined in tandem by RQ-PCR and six-color flow cytometry. Results: MRD results were concordant in 91 of the 108 paired samples (84.2%; K=0.690); 49 samples were MRD-negative while 42 were MRD-positive by both methods, with < 1 log difference in positive MRD estimates in 39 samples (92.9%). Of the 17 discordant samples, 16 were MRD-positive by RQ-PCR but MRD-negative by flow cytometry; the opposite was true in one sample. Kappa value/concordance was 0.690/85.0% (n = 60) for ETV6-RUNX1, 0.842/93.3% (n = 15) for TCF3-PBX1, and 0.535/78.8% (n = 33) for BCR-ABL1. Specific immunophenotypic abnormalities were more prevalent in each genetic subgroup, such as CD38 underexpression, CD58 overexpression, and CD34 overexpression in ETV6-RUNX1, TCF3-PBX1, and BCR-ABL1, respectively. Conclusion: In most follow-up samples, MRD estimates by two methods are in agreement, especially in patients with TCF3-PBX1.
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spelling doaj.art-3d1bcaee58e84ded9e8acaf630e741482022-12-21T19:17:32ZengElsevierJournal of the Formosan Medical Association0929-66462017-10-011161077478110.1016/j.jfma.2016.12.002Concordance of two approaches in monitoring of minimal residual disease in B-precursor acute lymphoblastic leukemia: Fusion transcripts and leukemia-associated immunophenotypesYing-Jung Huang0Elaine Coustan-Smith1Hsiao-Wen Kao2Hsi-Che Liu3Shih-Hsiang Chen4Chih-Cheng Hsiao5Chao-Ping Yang6Tang-Her Jaing7Ting-Chi Yeh8Ming-Chung Kuo9Chang-Liang Lai10Chia-Hui Chang11Dario Campana12Der-Cherng Liang13Lee-Yung Shih14Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanDepartment of Pediatrics, National University of Singapore, SingaporeDivision of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanDepartment of Pediatrics, Mackay Memorial Hospital and Mackay Medical College, Taipei, TaiwanCollege of Medicine, Chang Gung University, Taoyuan, TaiwanCollege of Medicine, Chang Gung University, Taoyuan, TaiwanDepartment of Hematology-Oncology, Chang Gung Children's Hospital at Linkou, Toayuan, TaiwanCollege of Medicine, Chang Gung University, Taoyuan, TaiwanDepartment of Pediatrics, Mackay Memorial Hospital and Mackay Medical College, Taipei, TaiwanDivision of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanDivision of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanDivision of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanDepartment of Pediatrics, National University of Singapore, SingaporeDepartment of Pediatrics, Mackay Memorial Hospital and Mackay Medical College, Taipei, TaiwanDivision of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanReal-time quantitative polymerase chain reaction (RQ-PCR) for fusion transcripts and flow cytometry for leukemia-specific markers are widely used for minimal residual disease (MRD) detection in acute lymphoblastic leukemia, but the relation between the results of either method is unclear. Methods: Mononucleated cells from 108 bone marrow samples collected from 55 B-precursor acute lymphoblastic leukemia patients (30 with t(12;21)/ETV6-RUNX1, 16 with t(9;22)/BCR-ABL1 and nine with t(1;19)/TCF3-PBX1) were examined in tandem by RQ-PCR and six-color flow cytometry. Results: MRD results were concordant in 91 of the 108 paired samples (84.2%; K=0.690); 49 samples were MRD-negative while 42 were MRD-positive by both methods, with < 1 log difference in positive MRD estimates in 39 samples (92.9%). Of the 17 discordant samples, 16 were MRD-positive by RQ-PCR but MRD-negative by flow cytometry; the opposite was true in one sample. Kappa value/concordance was 0.690/85.0% (n = 60) for ETV6-RUNX1, 0.842/93.3% (n = 15) for TCF3-PBX1, and 0.535/78.8% (n = 33) for BCR-ABL1. Specific immunophenotypic abnormalities were more prevalent in each genetic subgroup, such as CD38 underexpression, CD58 overexpression, and CD34 overexpression in ETV6-RUNX1, TCF3-PBX1, and BCR-ABL1, respectively. Conclusion: In most follow-up samples, MRD estimates by two methods are in agreement, especially in patients with TCF3-PBX1.http://www.sciencedirect.com/science/article/pii/S0929664616304806B-precursor acute lymphoblastic leukemiaflow cytometryfusion transcriptsminimal residual disease
spellingShingle Ying-Jung Huang
Elaine Coustan-Smith
Hsiao-Wen Kao
Hsi-Che Liu
Shih-Hsiang Chen
Chih-Cheng Hsiao
Chao-Ping Yang
Tang-Her Jaing
Ting-Chi Yeh
Ming-Chung Kuo
Chang-Liang Lai
Chia-Hui Chang
Dario Campana
Der-Cherng Liang
Lee-Yung Shih
Concordance of two approaches in monitoring of minimal residual disease in B-precursor acute lymphoblastic leukemia: Fusion transcripts and leukemia-associated immunophenotypes
Journal of the Formosan Medical Association
B-precursor acute lymphoblastic leukemia
flow cytometry
fusion transcripts
minimal residual disease
title Concordance of two approaches in monitoring of minimal residual disease in B-precursor acute lymphoblastic leukemia: Fusion transcripts and leukemia-associated immunophenotypes
title_full Concordance of two approaches in monitoring of minimal residual disease in B-precursor acute lymphoblastic leukemia: Fusion transcripts and leukemia-associated immunophenotypes
title_fullStr Concordance of two approaches in monitoring of minimal residual disease in B-precursor acute lymphoblastic leukemia: Fusion transcripts and leukemia-associated immunophenotypes
title_full_unstemmed Concordance of two approaches in monitoring of minimal residual disease in B-precursor acute lymphoblastic leukemia: Fusion transcripts and leukemia-associated immunophenotypes
title_short Concordance of two approaches in monitoring of minimal residual disease in B-precursor acute lymphoblastic leukemia: Fusion transcripts and leukemia-associated immunophenotypes
title_sort concordance of two approaches in monitoring of minimal residual disease in b precursor acute lymphoblastic leukemia fusion transcripts and leukemia associated immunophenotypes
topic B-precursor acute lymphoblastic leukemia
flow cytometry
fusion transcripts
minimal residual disease
url http://www.sciencedirect.com/science/article/pii/S0929664616304806
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