ETV6/RUNX1 fusion at diagnosis and relapse: some prognostic indications
ETV6/RUNX1 fusion at diagnosis and relapse: some prognostic indications
This study was undertaken in order to compare the interphase and metaphase cytogenetics of 28 patients with ETV6/RUNX1 positive acute lymphoblastic leukemia, at diagnosis and relapse. The median time to relapse was 26 months. The significant fusion positive population heterogeneity revealed at interphase by a commercial probe for ETV6/RUNX1 fusion has not been described before. Six diagnostic samples had a single abnormal population; others had up to five each, which differed in the numbers of RUNX1 signals, and in the retention or loss of the second ETV6 signal. In contrast, the number of fusion signals was more constant. At relapse, there were fewer populations; the largest or unique clone was sometimes a re-emergence of a minor, diagnostic one, with a retained copy of ETV6 and the most RUNX1 signals. Abnormal, fusion negative clones were identified in bone marrow samples at extra-medullary relapse. Variant three or four-way translocations, which involved chromosomes 12 and 21, were prominent among the complex rearrangements revealed by metaphase FISH. The frequency of their occurrence at diagnosis and reappearance at relapse, sometimes accompanied by minor clonal evolution, was another new observation. Other recurrent cytogenetic features included a second copy of the fusion signal in six cases, partial duplication of the long arm of the X chromosome in two cases, and trisomy 10 in three cases. In comparing our data with previously reported cases, a picture is beginning to emerge of certain diagnostic features, which may provide circumstantial evidence of an increased risk of relapse.
54-71
Martineau, Mary
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Jalali, G. Reza
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Barber, Kerry E.
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Broadfield, Zoë J.
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Cheung, Kan Luk
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Lilleyman, John
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Moorman, Anthony V.
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Richards, Sue
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Robinson, Hazel M.
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Ross, Fiona
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Harrison, Christine J.
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2005
Martineau, Mary
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Jalali, G. Reza
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Barber, Kerry E.
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Broadfield, Zoë J.
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Cheung, Kan Luk
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Lilleyman, John
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Moorman, Anthony V.
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Richards, Sue
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Robinson, Hazel M.
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Ross, Fiona
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Harrison, Christine J.
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Martineau, Mary, Jalali, G. Reza, Barber, Kerry E., Broadfield, Zoë J., Cheung, Kan Luk, Lilleyman, John, Moorman, Anthony V., Richards, Sue, Robinson, Hazel M., Ross, Fiona and Harrison, Christine J.
(2005)
ETV6/RUNX1 fusion at diagnosis and relapse: some prognostic indications.
Genes, Chromosomes and Cancer, 43 (1), .
(doi:10.1002/gcc.20158).
Abstract
This study was undertaken in order to compare the interphase and metaphase cytogenetics of 28 patients with ETV6/RUNX1 positive acute lymphoblastic leukemia, at diagnosis and relapse. The median time to relapse was 26 months. The significant fusion positive population heterogeneity revealed at interphase by a commercial probe for ETV6/RUNX1 fusion has not been described before. Six diagnostic samples had a single abnormal population; others had up to five each, which differed in the numbers of RUNX1 signals, and in the retention or loss of the second ETV6 signal. In contrast, the number of fusion signals was more constant. At relapse, there were fewer populations; the largest or unique clone was sometimes a re-emergence of a minor, diagnostic one, with a retained copy of ETV6 and the most RUNX1 signals. Abnormal, fusion negative clones were identified in bone marrow samples at extra-medullary relapse. Variant three or four-way translocations, which involved chromosomes 12 and 21, were prominent among the complex rearrangements revealed by metaphase FISH. The frequency of their occurrence at diagnosis and reappearance at relapse, sometimes accompanied by minor clonal evolution, was another new observation. Other recurrent cytogenetic features included a second copy of the fusion signal in six cases, partial duplication of the long arm of the X chromosome in two cases, and trisomy 10 in three cases. In comparing our data with previously reported cases, a picture is beginning to emerge of certain diagnostic features, which may provide circumstantial evidence of an increased risk of relapse.
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Published date: 2005
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Local EPrints ID: 24857
URI: http://eprints.soton.ac.uk/id/eprint/24857
ISSN: 1045-2257
PURE UUID: 91c261c7-a6cb-44be-acce-242c85c8ea52
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Date deposited: 03 Apr 2006
Last modified: 15 Mar 2024 06:58
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Contributors
Author:
Mary Martineau
Author:
G. Reza Jalali
Author:
Kerry E. Barber
Author:
Zoë J. Broadfield
Author:
Kan Luk Cheung
Author:
John Lilleyman
Author:
Anthony V. Moorman
Author:
Sue Richards
Author:
Hazel M. Robinson
Author:
Fiona Ross
Author:
Christine J. Harrison
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