The translocation t(1;19)(q23;p13) (TCF3/PBX1 fusion) is the most common recurrent genetic abnormality detected amongst patients with B-cell lymphoblastic leukaemia in Johannesburg, South Africa

SA Journal of Oncology

 
 
Field Value
 
Title The translocation t(1;19)(q23;p13) (TCF3/PBX1 fusion) is the most common recurrent genetic abnormality detected amongst patients with B-cell lymphoblastic leukaemia in Johannesburg, South Africa
 
Creator Vaughan, Jenifer Bouwer, Nikki Willem, Pascale Wiggill, Tracey Hodkinson, Katherine
 
Subject — B-cell acute lymphoblastic leukaemia; genetics; t(1;19); South Africa; epidemiology
Description Background: B-cell lymphoblastic leukaemia (B-ALL) is a malignancy of immature B-cells with several described recurrent genetic abnormalities. These have distinct clinico-pathological associations and show regional variation in prevalence. In all previously reported series, the translocation t(1;19) is uncommon, comprising 10% of all cases. The genetic composition of B-ALL in Africa is unknown.Aim: The aim of this study was to assess the genetic landscape of B-ALL in Johannesburg, South Africa.Setting: The Johannesburg state-sector.Methods: All cases of B-ALL diagnosed by flow cytometry in the state-sector hospitals of Johannesburg over 36 months between 2016 and 2019 were identified and pertinent data were recorded from the laboratory information system.Results: A total of 108 patients with B-ALL were identified, 82 (75.9%) of whom were children or adolescents. The translocation t(1;19)(q23;p13) was the most common genetic abnormality identified (23.7% of cases), predominating in young patients. The translocation t(9;22)(q34;q11) was the next most common aberration (17.5%) occurring predominantly in adults 40 years of age, but also in 8.1% of children. Crude survival rates were overall poor (44.6% overall and 57.4% in patients 18 years of age). On survival analysis, older age, KMT2A-rearrangement and t(1;19) were independently associated with relapse-related death. The t(9;22) was not associated with mortality independently from age.Conclusion: B-ALL shows a distinct pattern of lymphoblastic leukaemia-associated chromosomal translocations in Johannesburg.
 
Publisher AOSIS
 
Contributor
Date 2021-07-06
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — —
Format text/html application/epub+zip text/xml application/pdf
Identifier 10.4102/sajo.v5i0.179
 
Source South African Journal of Oncology; Vol 5 (2021); 6 pages 2523-0646 2518-8704
 
Language eng
 
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https://sajo.org.za/index.php/sajo/article/view/179/496 https://sajo.org.za/index.php/sajo/article/view/179/497 https://sajo.org.za/index.php/sajo/article/view/179/498 https://sajo.org.za/index.php/sajo/article/view/179/499
 
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Rights Copyright (c) 2021 Jenifer Vaughan, Nikki Bouwer, Tracey Wiggill, Pascale Willem, Katherine Hodkinson https://creativecommons.org/licenses/by/4.0
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