Blast phase of chronic myeloid leukemia with concurrent BCR::ABL1 and SET::NUP214: A report of two cases

被引:3
|
作者
Chen, Yan [1 ]
Wang, Qian [1 ]
Cen, Jiannong [1 ]
Xu, Chao [1 ]
Tao, Ting-ting [1 ]
Xie, Jundan [1 ]
Shen, Wenhong [1 ]
Gong, Yanlei [1 ]
Pan, Jinlan [1 ]
Yao, Li [1 ,2 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, NHC Key Lab Thrombosis & Hemostasis, Jiangsu Inst Hematol,Natl Clin Res Ctr Hematol Di, Suzhou, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
BCR; ABL1; blast phase; chronic myeloid leukemia; SET; NUP214; CHRONIC MYELOGENOUS LEUKEMIA; FUSION GENES; SET-NUP214; IMPACT; ERA; RESISTANCE; FEATURES; CML;
D O I
10.1002/mc.23480
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm defined by the presence of t(9;22)(q34;q11.2)/BCR::ABL1. Additional chromosomal abnormalities play an important role in the progression to CML. However, the additional fusion gene was rarely reported such as CBFB::MYH11. In this report, we described two cases of the co-occurrence of BCR::ABL1 and SET::NUP214 in CML-BP for the first time, which is associated with poor outcomes during tyrosine kinase inhibitor (TKI) treatment. Meanwhile, we retrospectively analyzed SET::NUP214 fusion transcript of the two cases at initial diagnosis of the CML chronic phase by quantitative RT-PCR, and detected at a ratio of 1.63% and 1.50%, respectively. SET::NUP214 may promote disease progression during the transformation of CML. This study highlights the importance of extended molecular testing at the initial diagnosis of CML-CP at TKI resistance and/or disease transformation.
引用
收藏
页码:117 / 121
页数:5
相关论文
共 50 条
  • [1] Aleukemic Chronic Myeloid Leukemia Without Neutrophilia and Thrombocytosis: a Report From the BCR::ABL1 Pathology Group
    Rivera, Daniel
    Cui, Wei
    Gao, Juehua
    Peker, Deniz
    Zhang, Qian-Yun
    Dewar, Rajan
    Qiu, Lianqun
    Konoplev, Sergej
    Hu, Zhihong
    Sasaki, Koji
    Hu, Aileen Y.
    Shuyu, E.
    Liu, Meng
    Fang, Hong
    Wang, Wei
    Tang, Guilin
    Apperley, Jane F.
    Hochhaus, Andreas
    Cortes, Jorge E.
    Khoury, Joseph D.
    Medeiros, L. Jeffrey
    Jabbour, Elias
    Hu, Shimin
    MODERN PATHOLOGY, 2024, 37 (02)
  • [2] Distribution of BCR–ABL1 Transcript Variants in Nigerians with Chronic Myeloid Leukemia
    Temilola O. Owojuyigbe
    Muheez A. Durosinmi
    Ramoni A. A. Bolarinwa
    Lateef Salawu
    Norah O. Akinola
    Abdulwaheed A. Ademosun
    Oluwayomi T. Bosede
    Indian Journal of Hematology and Blood Transfusion, 2020, 36 : 646 - 651
  • [3] Frequencies of BCR::ABL1 Transcripts in Patients with Chronic Myeloid Leukemia: A Meta-Analysis
    Romero-Morelos, Pablo
    Gonzalez-Yebra, Ana Lilia
    Munoz-Lopez, Daniela
    Lara-Lona, Elia
    Gonzalez-Yebra, Beatriz
    GENES, 2024, 15 (02)
  • [4] Cytogenetic, fluorescence in situ hybridization, and molecular characterization of chronic myeloid leukemia in chronic phase with four BCR/ABL1 fusion signals: a case report
    Teresa Vargas, Maria
    Angeles Portero, Maria
    Rodriguez, Alicia
    Reyes, Juana
    Fernandez-Novoa, Carmen
    CANCER GENETICS AND CYTOGENETICS, 2009, 195 (01) : 71 - 74
  • [5] Variant-specific BCR::ABL1 quantification discrepancy in chronic myeloid leukemia
    Jacobs, Koen
    Moerman, Alena
    Vandepoele, Karl
    Van den Abeele, Tim
    De Mulder, Katrien
    Steel, Eva
    Clauwaert, Maxim
    Louagie, Henk
    INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2024, 46 (05) : 910 - 917
  • [6] Deciphering Potential Molecular Signatures to Differentiate Acute Myeloid Leukemia (AML) with BCR::ABL1 from Chronic Myeloid Leukemia (CML) in Blast Crisis
    Boucher, Lara
    Sorel, Nathalie
    Desterke, Christophe
    Chollet, Melanie
    Rozalska, Laura
    Gallego Hernanz, Maria Pilar
    Cayssials, Emilie
    Raimbault, Anna
    Bennaceur-Griscelli, Annelise
    Turhan, Ali G.
    Chomel, Jean-Claude
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (20)
  • [7] Imatinib Sensitivity in BCR-ABL1-Positive Chronic Myeloid Leukemia Cells Is Regulated by the Remaining Normal ABL1 Allele
    Virgili, Anna
    Koptyra, Mateusz
    Dasgupta, Yashodhara
    Glodkowska-Mrowka, Eliza
    Stoklosa, Tomasz
    Nacheva, Elisabeth P.
    Skorski, Tomasz
    CANCER RESEARCH, 2011, 71 (16) : 5381 - 5386
  • [8] From the archives of MD Anderson Cancer Center: Concurrent BCR-ABL1 and CRLF2 rearrangements in B-lymphoblast phase of chronic myeloid leukemia
    Thakral, Beenu
    Jain, Nitin
    Tang, Guilin
    Konoplev, Sergej
    Vega, Francisco
    Medeiros, L. Jeffrey
    Wang, Sa A.
    ANNALS OF DIAGNOSTIC PATHOLOGY, 2021, 53
  • [9] Continuous therapy response references for BCR::ABL1 monitoring in pediatric chronic myeloid leukemia
    Volz, Christian
    Zerjatke, Thomas
    Gottschalk, Andrea
    Semper, Sabine
    Suttorp, Meinolf
    Glauche, Ingmar
    Krumbholz, Manuela
    Metzler, Markus
    SCIENTIFIC REPORTS, 2023, 13 (01)
  • [10] Chronic Myeloid Leukemia: Beyond BCR-ABL1
    Zhou, Ting
    Medeiros, L. Jeffrey
    Hu, Shimin
    CURRENT HEMATOLOGIC MALIGNANCY REPORTS, 2018, 13 (06) : 435 - 445