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Trisomy 8 in pediatric acute myeloid leukemia : A NOPHO-AML study

Laursen, Anne Cathrine Lund (författare)
Aarhus Univ Hosp, Dept Pediat, Aarhus, Denmark.
Sandahl, Julie Damgaard (författare)
Aarhus Univ Hosp, Dept Pediat, Aarhus, Denmark.
Kjeldsen, Eigil (författare)
Aarhus Univ Hosp, Dept Hematol, Canc Cytogenet Lab, Aarhus, Denmark.
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Abrahamsson, Jonas, 1954 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
Asdahl, Peter (författare)
Aarhus Univ Hosp, Dept Pediat, Aarhus, Denmark.
Ha, Shau-Yin (författare)
Queen Mary Hosp, Dept Pediat, Hong Kong, Hong Kong, Peoples R China.;HKPHOSG, Hong Kong, Hong Kong, Peoples R China.
Heldrup, Jesper (författare)
Univ Hosp, Dept Pediat, Lund, Sweden.
Jahnukainen, Kirsi (författare)
Univ Helsinki, Childrens Hosp, Cent Hosp, Helsinki, Finland.
Jonsson, Olafur G. (författare)
Landspitalinn, Dept Pediat, Reykjavik, Iceland.
Lausen, Birgitte (författare)
Univ Copenhagen, Dept Pediat & Adolescent Med, Rigshosp, Copenhagen, Denmark.
Palle, Josefine (författare)
Uppsala universitet,Pediatrik
Zeller, Bernward (författare)
Oslo Univ Hosp, Dept Pediat Med, Oslo, Norway.
Forestier, Erik (författare)
Umea Univ Hosp, Dept Biosci, Clin Genet, Umea, Sweden.,Department of Medical Biosciences, Clinical Genetics, Umeå University Hospital, Umeå, Sweden
Hasle, Henrik (författare)
Aarhus Univ Hosp, Dept Pediat, Aarhus, Denmark.
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Aarhus Univ Hosp, Dept Pediat, Aarhus, Denmark Aarhus Univ Hosp, Dept Hematol, Canc Cytogenet Lab, Aarhus, Denmark. (creator_code:org_t)
2016-06-23
2016
Engelska.
Ingår i: Genes, Chromosomes and Cancer. - : Wiley. - 1045-2257 .- 1098-2264. ; 55:9, s. 719-726
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Trisomy 8 (+8) is a common cytogenetic aberration in acute myeloid leukemia (AML); however, the impact of +8 in pediatric AML is largely unknown. We retrospectively investigated 609 patients from the NOPHO-AML database to determine the clinical and cytogenetic characteristics of +8 in pediatric AML and to investigate its prognostic impact. Complete cytogenetic data were available in 596 patients (98%) aged 0-18 years, diagnosed from 1993 to 2012, and treated according to the NOPHO-AML 1993 and 2004 protocols in the Nordic countries and Hong Kong. We identified 86 patients (14%) with +8. Trisomy 8 was combined with other cytogenetic aberrations in 68 patients (11%) (+8 other) and in 18 patients (3%), it was the sole abnormality (+8 alone). Trisomy 8 was associated with FAB M5 (36%) but otherwise clinically comparable with non-trisomy 8 patients. Trisomy 8 was favorable in patients of young age and with t(9;11). Trisomy 8 alone was associated with older age (median age 10.1 years), FAB M2 (33%), and FLT3-ITD mutations (58%). The 5-year event-free survival for patients with +8 alone was 50% and 5-year overall survival was 75%. In conclusion, +8 is one of the most common cytogenetic aberrations in pediatric AML. Trisomy 8 positive AML is a heterogeneous group and the majority of cases have additional cytogenetic aberrations. Patients with +8 alone differed from patients with +8 other and were associated with older age, FAB M2, and FLT3-ITD aberrations. There were no differences in survival despite the more frequent occurrence of FLT3-ITD in +8 alone.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)

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