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FältnamnIndikatorerMetadata
00004155naa a2200685 4500
001oai:DiVA.org:umu-42549
003SwePub
008110408s2009 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-425492 URI
024a https://doi.org/10.1182/blood-2009-04-2151522 DOI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Balgobind, Brian V4 aut
2451 0a Novel prognostic subgroups in childhood 11q23/MLL-rearranged acute myeloid leukemia :b results of an international retrospective study.
264 1b American Society of Hematology,c 2009
338 a print2 rdacarrier
520 a Translocations involving chromosome 11q23 frequently occur in pediatric acute myeloid leukemia (AML) and are associated with poor prognosis. In most cases, the MLL gene is involved, and more than 50 translocation partners have been described. Clinical outcome data of the 11q23-rearranged subgroups are scarce because most 11q23 series are too small for meaningful analysis of subgroups, although some studies suggest that patients with t(9;11)(p22;q23) have a more favorable prognosis. We retrospectively collected outcome data of 756 children with 11q23- or MLL-rearranged AML from 11 collaborative groups to identify differences in outcome based on translocation partners. All karyotypes were centrally reviewed before assigning patients to subgroups. The event-free survival of 11q23/MLL-rearranged pediatric AML at 5 years from diagnosis was 44% (+/- 5%), with large differences across subgroups (11% +/- 5% to 92% +/- 5%). Multivariate analysis identified the following subgroups as independent prognostic predictors: t(1;11)(q21;q23) (hazard ratio [HR] = 0.1, P = .004); t(6;11)(q27;q23) (HR = 2.2, P < .001); t(10;11)(p12;q23) (HR = 1.5, P = .005); and t(10;11)(p11.2;q23) (HR = 2.5, P = .005). We could not confirm the favorable prognosis of the t(9;11)(p22;q23) subgroup. We identified large differences in outcome within 11q23/MLL-rearranged pediatric AML and novel subgroups based on translocation partners that independently predict clinical outcome. Screening for these translocation partners is needed for accurate treatment stratification at diagnosis.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Pediatrik0 (SwePub)302212 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Pediatrics0 (SwePub)302212 hsv//eng
700a Raimondi, Susana C4 aut
700a Harbott, Jochen4 aut
700a Zimmermann, Martin4 aut
700a Alonzo, Todd A4 aut
700a Auvrignon, Anne4 aut
700a Beverloo, H Berna4 aut
700a Chang, Myron4 aut
700a Creutzig, Ursula4 aut
700a Dworzak, Michael N4 aut
700a Forestier, Eriku Umeå universitet,Pediatrik4 aut0 (Swepub:umu)erfo0007
700a Gibson, Brenda4 aut
700a Hasle, Henrik4 aut
700a Harrison, Christine J4 aut
700a Heerema, Nyla A4 aut
700a Kaspers, Gertjan J L4 aut
700a Leszl, Anna4 aut
700a Litvinko, Nathalia4 aut
700a Nigro, Luca Lo4 aut
700a Morimoto, Akira4 aut
700a Perot, Christine4 aut
700a Pieters, Rob4 aut
700a Reinhardt, Dirk4 aut
700a Rubnitz, Jeffrey E4 aut
700a Smith, Franklin O4 aut
700a Stary, Jan4 aut
700a Stasevich, Irina4 aut
700a Strehl, Sabine4 aut
700a Taga, Takashi4 aut
700a Tomizawa, Daisuke4 aut
700a Webb, David4 aut
700a Zemanova, Zuzana4 aut
700a Zwaan, C Michel4 aut
700a van den Heuvel-Eibrink, Marry M4 aut
710a Umeå universitetb Pediatrik4 org
773t Bloodd : American Society of Hematologyg 114:12, s. 2489-2496q 114:12<2489-2496x 0006-4971x 1528-0020
856u https://europepmc.org/articles/pmc2927031
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-42549
8564 8u https://doi.org/10.1182/blood-2009-04-215152

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