Correlation of BCR/ABL transcript variants with patients’ characteristics in childhood chronic myeloid leukaemia

European Journal of Haematology - Tập 82 Số 2 - Trang 112-118 - 2009
Ronald D. Adler1, Susanne Viehmann2, Eberhard Kuhlisch3, Yvonne Martiniak1, Silja Röttgers2, Jochen Harbott2, Meinolf Suttorp1
1Division of Paediatric Haematology and Oncology, University Hospital Carl Gustav Carus, Technical University at Dresden, Dresden, Germany
2Oncogenetic Laboratory, Paediatric Haematology and Oncology, Justus‐Liebig‐University, Giessen, Germany
3Institute of Medical Informatics and Biometry, University Hospital Carl Gustav Carus, Technical University at Dresden, Dresden, Germany

Tóm tắt

Abstract

Background and objective:  The characteristic chromosomal translocation t(9;22)(q34;q11) in chronic myeloid leukaemia (CML) mainly results in the two different BCR/ABL fusion transcripts b2a2 or b3a2. Both transcript variants can occur simultaneously due to alternative splicing of the b3a2 transcript. Conflicting results have been reported on the influence of the transcripts on haematological findings at diagnosis and the course of the disease in adults while data concerning these topics on childhood CML are still missing. This paper reports on a correlation of BCR/ABL transcript variants with patients’ characteristics in childhood CML.

Design and methods:  Transcript types were determined in 146 paediatric patients with CML enrolled in trial CML‐paed‐I. Fifty‐five patients (38%) expressed b2a2, 53 patients (36%) b3a2 and 38 patients (26%) both transcripts, respectively. These findings were correlated with patients’ characteristics (sex, age, WBC, Hb, platelet count, hepatosplenomegaly, etc.) assessed at diagnosis.

Results:  While the co‐expression of both transcripts was evenly distributed among genders [b2a2 + b3a2: 22 females (28%), 16 males (24%)] a highly significant difference (P = 0.007) was found concerning the expression of the b2a2 transcript [34 male (51%) vs. 21 female (27%)] and vice versa of the b3a2 transcript [17 male (25%) vs. 36 female (45%)]. High platelet counts and the combination of high platelet counts in conjunction with pronounced leukocytosis were observed more often in patients expressing the b3a2 transcript.

Conclusions:  These findings demonstrate that in children like in adults specific BCR/ABL transcript types present at diagnosis are associated with distinct haematological alterations (e.g. a high platelet count with the transcript b3a2). However, the sex‐dependent skewed distribution of the BCR/ABL transcript types observed so far in this paediatric cohort only deserves further investigation.

Từ khóa


Tài liệu tham khảo

10.1056/NEJM199904293401706

10.1111/j.1365-2141.1994.tb06734.x

10.1046/j.1365-2141.2002.03508.x

10.1046/j.1365-2141.1998.00945.x

10.1542/peds.2004-2473

10.1038/sj.leu.2401929

10.1016/0959-8049(94)00449-F

Inokuchi K, 1991, A possible correlation between the type of BCR/ABL hybrid messenger RNA and platelet count in Philadelphia‐positive chronic myelogenous leukemia, Blood, 78, 3125, 10.1182/blood.V78.12.3125.3125

10.1016/S0959-8049(00)00128-3

10.1038/bmt.2008.282

10.1016/j.cancergencyto.2006.01.015

10.1055/s-2008-1046480

Suttorp M, 2004, Chronic myeloid leukemia (CML) in childhood – results of the multicenter trial CML‐paed, Blood, 104, 178a

Shaffer LG, 2005, ISCN 2005: An International System for Human Cytogenetic Nomenclature

10.1016/0003-2697(87)90021-2

Harbott J, 1997, Incidence of TEL/AML1 fusion gene consecutively analyzed in children with relapse of acute lymphoblastic leukemia (ALL), Blood, 90, 4933, 10.1182/blood.V90.12.4933

Melo JV, 1996, The molecular biology of chronic myeloid leukaemia, Leukemia, 10, 751

Aurer I, 1991, BCR/ABL rearrangements in children with Philadelphia chromosome‐positive chronic myelogenous leukemia, Blood, 78, 2407, 10.1182/blood.V78.9.2407.2407

Ruiz‐Argüelles GJ, 2004, Frequencies of the breakpoint cluster region types of the BCR/ABL fusion gene in Mexican Mestizo patients with chronic myelogenous leukemia, Rev Invest Clin, 56, 605

10.1046/j.1365-2257.2002.00413.x

10.1038/sj.leu.2403756

10.1046/j.1365-2141.2003.04458.x

10.1038/sj.leu.2404670

10.1111/j.0953-8194.2004.01154.x

10.1016/j.neulet.2005.02.014

10.1016/j.febslet.2005.07.069

10.1242/dev.02415

10.1111/j.1365-2141.1995.tb08362.x

10.1046/j.1365-2141.1996.00350.x

10.1016/j.trsl.2006.07.002

Wacker MJ, 2008, Sex difference in the association of the anngiotensin converting enzyme I/D polymorphism and body mass index, Med Sci Monit, 14, 353

10.1371/journal.pgen.0030099