Frequency of TP53 Mutation in B-Cell Chronic Lymphocytic Leukaemia and its Association with Lymphocyte Doubling Time

被引:0
|
作者
Ali, Syeda Mah [1 ]
Irfan, Syed Muhammad [1 ]
Raza, Naila [1 ]
机构
[1] Liaquat Natl Hosp, Dept Haematol, Karachi, Pakistan
来源
JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN | 2023年 / 33卷 / 11期
关键词
TP53; mutation; B-Cell chronic lymphocytic leukaemia (B-CLL); Lymphocyte doubling time (LDT); IMPACT; GENE;
D O I
10.29271/jcpsp.2023.11.1249
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To determine the frequency of TP53 mutation at diagnosis of B-cell Chronic Lymphocytic Leukaemia (B-CLL) in Pakistani patients, and to investigate whether lymphocyte doubling time (LDT) of less than 1 year could be used as a surrogate marker for TP53 mutation. Study Design: A cross-sectional descriptive study. Place and Duration of the Study: Department of Haematology, Liaquat National Hospital, from January 2020 to December 2022. Methodology: Patients diagnosed with B-CLL based on the criteria set by International Workshop on Chronic Lymphocytic Leukaemia were included in the study. Clinico-haematological parameters were recorded, and TP53 mutation analysis was performed by fluorescence in situ hybridisation. Patients were followed every 3-6 months after diagnosis with the recent complete blood count (CBC) reports to record CBC parameters and calculate LDT. Results: A total of 128 B-CLL cases were evaluated, with a mean age of 62 years. Among these cases, 10 patients (7.8%) tested positive for TP53 mutation, while 118 patients (92.2%) tested negative. During the follow-up period, 26 patients were lost to follow-up, with only one patient from the TP53 positive group. In the TP53 positive group, 55.6% (n=5/9) patients had an LDT of less than 1 year, indicating aggressive disease compared to 30.1% (n=28/93) patients in the negative group (p <0.1). Conclusion: TP53 mutations may be associated with shorter LDT, indicating aggressive disease. Further research is needed to fully comprehend the relationship between TP53 mutation and LDT in B-CLL.
引用
收藏
页码:1249 / 1253
页数:5
相关论文
共 50 条
  • [21] Dysregulation of T lymphocyte activation markers in B-cell chronic lymphocytic leukaemia.
    Scrivener, S
    Prentice, AG
    Kaminski, ER
    Demaine, A
    Kruger, AR
    BLOOD, 1999, 94 (10) : 304B - 305B
  • [22] Cutaneous T-lymphocyte infiltrate associated with B-cell chronic lymphocytic leukaemia
    Bateman, AC
    Hodges, E
    Quin, CT
    McCormick, D
    Barrett, D
    Smith, JL
    HISTOPATHOLOGY, 1999, 34 (02) : 183 - 184
  • [23] TP53 mutation and survival in aggressive B cell lymphoma
    Zenz, Thorsten
    Kreuz, Markus
    Fuge, Maxi
    Klapper, Wolfram
    Horn, Heike
    Staiger, Annette M.
    Winter, Doris
    Helfrich, Hanne
    Huellein, Jennifer
    Hansmann, Martin-Leo
    Stein, Harald
    Feller, Alfred
    Moeller, Peter
    Schmitz, Norbert
    Truemper, Lorenz
    Loeffler, Markus
    Siebert, Reiner
    Rosenwald, Andreas
    Ott, German
    Pfreundschuh, Michael
    Stilgenbauer, Stephan
    INTERNATIONAL JOURNAL OF CANCER, 2017, 141 (07) : 1381 - 1388
  • [24] The gene expression signature associated with TP53 mutation/deletion in chronic lymphocytic leukaemia is dominated by the under-expression of TP53 and other genes on chromosome 17p
    Lin, Ke
    Lane, Brian
    Carter, Anthony
    Johnson, Gillian G.
    Onwuazor, Obiageli
    Oates, Melanie
    Zenz, Thorsten
    Stilgenbauer, Stephan
    Atherton, Mark
    Douglas, Angela
    Ebrahimi, Bahram
    Sherrington, Paul D.
    Pettitt, Andrew R.
    BRITISH JOURNAL OF HAEMATOLOGY, 2013, 160 (01) : 53 - 62
  • [25] TP53 Pro72 allele potentially increases the poor prognostic significance of TP53 mutation in chronic lymphocytic leukemia
    Hua-Jie Dong
    Cheng Fang
    Li Wang
    Lei Fan
    Ji Xu
    Jia-Zhu Wu
    Ting-Xun Lu
    Jian-Yong Li
    Wei Xu
    Medical Oncology, 2014, 31
  • [26] TP53 Pro72 allele potentially increases the poor prognostic significance of TP53 mutation in chronic lymphocytic leukemia
    Dong, Hua-Jie
    Fang, Cheng
    Wang, Li
    Fan, Lei
    Xu, Ji
    Wu, Jia-Zhu
    Lu, Ting-Xun
    Li, Jian-Yong
    Xu, Wei
    MEDICAL ONCOLOGY, 2014, 31 (04)
  • [27] High frequency of surface immunoglobulin IgG in B-Cell chronic lymphocytic leukaemia
    Wiseman, Catherine
    Giustiniani, Jerome
    Mikkelsen, Lene
    Macey, Marion
    Goff, Lindsey
    Gribben, John
    Agrawal, Samir
    BLOOD, 2007, 110 (11) : 245B - 245B
  • [28] B-cell Receptor Signaling Induced Metabolic Alterations in Chronic Lymphocytic Leukemia Can Be Partially Bypassed by TP53 Abnormalities
    Kluckova, Katarina
    Clear, Andrew J.
    D'Avola, Annalisa
    Rassenti, Laura Z.
    Kipps, Thomas J.
    Gribben, John G.
    Riches, John C.
    HEMASPHERE, 2022, 6 (06): : E722
  • [29] TP53 dysfunction in chronic lymphocytic leukemia: clinical relevance in the era of B-cell receptors and BCL-2 inhibitors
    Morabito, Fortunato
    Gentile, Massimo
    Monti, Paola
    Recchia, Anna Grazia
    Menichini, Paola
    Skafi, Mamdouh
    Atrash, Moien
    De Luca, Giuseppa
    Bossio, Sabrina
    Al-Janazreh, Hamdi
    Galimberti, Sara
    Salah, Zaidoun
    Morabito, Lucio
    Mujahed, Alham
    Hindiyeh, Musa
    Dono, Mariella
    Fais, Franco
    Cutrona, Giovanna
    Neri, Antonino
    Tripepi, Giovanni
    Fronza, Gilberto
    Ferrarini, Manlio
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2020, 29 (08) : 869 - 880
  • [30] A new hope: novel therapeutic approaches to treatment of chronic lymphocytic leukaemia with defects in TP53
    Shindiapina, Polina
    Brown, Jennifer R.
    Danilov, Alexey V.
    BRITISH JOURNAL OF HAEMATOLOGY, 2014, 167 (02) : 149 - 161