作者
Brian V Balgobind, Susana C Raimondi, Jochen Harbott, Martin Zimmermann, Todd A Alonzo, Anne Auvrignon, H Berna Beverloo, Myron Chang, Ursula Creutzig, Michael N Dworzak, Erik Forestier, Brenda Gibson, Henrik Hasle, Christine J Harrison, Nyla A Heerema, Gertjan JL Kaspers, Anna Leszl, Nathalia Litvinko, Luca Lo Nigro, Akira Morimoto, Christine Perot, Rob Pieters, Dirk Reinhardt, Jeffrey E Rubnitz, Franklin O Smith, Jan Stary, Irina Stasevich, Sabine Strehl, Takashi Taga, Daisuke Tomizawa, David Webb, Zuzana Zemanova, C Michel Zwaan, Marry M Van Den Heuvel-Eibrink
发表日期
2009/9/17
期刊
Blood, The Journal of the American Society of Hematology
卷号
114
期号
12
页码范围
2489-2496
出版商
American Society of Hematology
简介
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 …
引用总数
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