Flow cytometric characterisation of acute leukaemia in adolescent and adult Ethiopians

被引:0
作者
Alemu, Jemal [1 ,2 ,3 ]
Gumi, Balako [3 ]
Tsegaye, Aster [1 ]
Sherif, Abdulaziz [4 ]
Tadesse, Fisihatsion [4 ]
Gebremedhin, Amha [4 ]
Howe, Rawleigh [2 ]
机构
[1] Addis Ababa Univ, Coll Hlth Sci, Dept Med Lab Sci, Addis Ababa, Ethiopia
[2] Armauer Hansen Res Inst, Addis Ababa, Ethiopia
[3] Addis Ababa Univ, Aklilu Lemma Inst Pathobiol, Addis Ababa, Ethiopia
[4] Addis Ababa Univ, Coll Hlth Sci, Dept Internal Med, Addis Ababa, Ethiopia
关键词
flow cytometry; acute leukaemia; Ethiopia; phenotype; cell surface biomarker; cytoplasmic biomarker; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; B-CELL; EXPRESSION; CLASSIFICATION; IMMUNOPHENOTYPE; MUTATIONS; DIAGNOSIS; SUBGROUP; IMPACT;
D O I
10.4102/ajlm.v14i1.2394
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Flow cytometric characterisation of acute leukaemia is a key diagnostic approach for clinical management of patients, but is minimally practised in resource-constrained settings like Ethiopia. Objective: This study aimed to determine the immunophenotypes of acute leukaemia by flow cytometry at Tikur Anbessa Specialised Hospital, Addis Ababa, Ethiopia. Methods: A cross-sectional study was conducted on adolescent and adult inpatients consecutively admitted from April 2019 to June 2021. Peripheral blood samples were stained for surface and cytoplasmic markers, and analysed by four-colour flow cytometry. Results: Of 140 cases aged 13 years to 76 years, 74 (53%) were men and 66 (47%) were women, 68 (49%) had acute lymphocytic leukaemia (ALL), 65 (46 %) had acute myelogenous leukaemia (AML), and 7 (5.0%) had acute leukaemia non-otherwise specified. Acute lymphocytic leukaemia was more common among adolescent and male cases; AML was more common among adult and female cases. Among ALL subtypes, B-cell acute lymphocytic leukaemia cases (73.5%) were more common than T-cell acute lymphocytic leukaemia (26.5%). A subset of acute leukaemia, CD19+/CD56+ AML was identified in 3 cases (6% of AML). Of the B-cell ALL cases, 21 (42%) were CD34+/CD10+/CD66c+, 10% were CD34+/CD10+/CD66c-, 32% were CD34-/CD10+, and 6% were CD34+/CD10-. An unexpectedly high number of T-cell ALL cases that lacked surface CD3 were observed to have significantly higher levels of aberrantly expressed myeloid markers. Conclusion: We observed multiple phenotypes identifying subtypes of acute leukaemia cases, extending our previous studies in Ethiopia. What this study adds: This study extends previous studies by describing phenotypically defined subsets of ALL and AML which, in addition to diagnosis, may have useful prognostic value for clinicians.
引用
收藏
页数:10
相关论文
共 47 条
  • [1] The genetic basis and cell of origin of mixed phenotype acute leukaemia
    Alexander, Thomas B.
    Gu, Zhaohui
    Iacobucci, Ilaria
    Dickerson, Kirsten
    Choi, John K.
    Xu, Beisi
    Payne-Turner, Debbie
    Yoshihara, Hiroki
    Loh, Mignon L.
    Horan, John
    Buldini, Barbara
    Basso, Giuseppe
    Elitzur, Sarah
    de Haas, Valerie
    Zwaan, C. Michel
    Yeoh, Allen
    Reinhardt, Dirk
    Tomizawa, Daisuke
    Kiyokawa, Nobutaka
    Lammens, Tim
    De Moerloose, Barbara
    Catchpoole, Daniel
    Hori, Hiroki
    Moorman, Anthony
    Moore, Andrew S.
    Hrusak, Ondrej
    Meshinchi, Soheil
    Orgel, Etan
    Devidas, Meenakshi
    Borowitz, Michael
    Wood, Brent
    Heerema, Nyla A.
    Carrol, Andrew
    Yang, Yung-Li
    Smith, Malcolm A.
    Davidsen, Tanja M.
    Hermida, Leandro C.
    Gesuwan, Patee
    Marra, Marco A.
    Ma, Yussanne
    Mungall, Andrew J.
    Moore, Richard A.
    Jones, Steven J. M.
    Valentine, Marcus
    Janke, Laura J.
    Rubnitz, Jeffrey E.
    Pui, Ching-Hon
    Ding, Liang
    Liu, Yu
    Zhang, Jinghui
    [J]. NATURE, 2018, 562 (7727) : 373 - +
  • [2] Allford S, 1999, BRIT J HAEMATOL, V105, P198
  • [3] Myeloperoxidase gene expression in infant leukemia: A pediatric oncology group study
    Alvarado, CS
    Austin, GE
    Borowitz, MJ
    Shuster, JJ
    Carroll, AJ
    Austin, ED
    Zhou, MX
    Zaki, SR
    Pullen, J
    [J]. LEUKEMIA & LYMPHOMA, 1998, 29 (1-2) : 145 - 160
  • [4] The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia
    Arber, Daniel A.
    Orazi, Attilio
    Hasserjian, Robert
    Thiele, Jurgen
    Borowitz, Michael J.
    Le Beau, Michelle M.
    Bloomfield, Clara D.
    Cazzola, Mario
    Vardiman, James W.
    [J]. BLOOD, 2016, 127 (20) : 2391 - 2405
  • [5] BENE MC, 1995, LEUKEMIA, V9, P1783
  • [6] Pro-B-cell to pre-B-cell development in B-lineage acute lymphoblastic leukemia expressing the MLL/AF4 fusion protein
    Bertrand, FE
    Vogtenhuber, C
    Shah, N
    LeBien, TW
    [J]. BLOOD, 2001, 98 (12) : 3398 - 3405
  • [7] BOROWITZ MJ, 1993, BLOOD, V82, P1086
  • [8] Is hyperdiploidy a favorable cytogenetics in adults with B-lymphoblastic leukemia?
    Chen, Zhining
    Sun, Yi
    Xie, Wei
    Wang, Sa A.
    Hu, Shimin
    Li, Shaoying
    Tang, Zhenya
    Toruner, Gokce
    Medeiros, L. Jeffrey
    Tang, Guilin
    [J]. CANCER MEDICINE, 2019, 8 (09): : 4093 - 4099
  • [9] Cytogenetic profile of de novo acute myeloid leukemia: a study based on 1432 patients in a single institution of China
    Cheng, Y.
    Wang, Y.
    Wang, H.
    Chen, Z.
    Lou, J.
    Xu, H.
    Wang, H.
    Qian, W.
    Meng, H.
    Lin, M.
    Jin, J.
    [J]. LEUKEMIA, 2009, 23 (10) : 1801 - 1806
  • [10] Flow Cytometry Rapidly Identifies All Acute Promyelocytic Leukemias With High Specificity Independent of Underlying Cytogenetic Abnormalities
    Dong, Henry Y.
    Kung, Jia Xue
    Bhardwaj, Vatsala
    McGill, John
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2011, 135 (01) : 76 - 84