Acute myeloid leukaemia with myelodysplastic features in children: a report of Japanese Paediatric Leukaemia/Lymphoma Study Group

被引:17
作者
Kinoshita, Akitoshi [1 ]
Miyachi, Hayato [2 ]
Matsushita, Hiromichi [2 ]
Yabe, Miharu [2 ]
Taki, Tomohiko [3 ]
Watanabe, Tomoyuki [4 ]
Saito, Akiko M. [5 ]
Tomizawa, Daisuke [6 ]
Taga, Takashi [7 ]
Takahashi, Hiroyuki [8 ]
Matsuo, Hidemasa [9 ]
Kodama, Kumi [9 ]
Ohki, Kentaro [10 ]
Hayashi, Yasuhide [10 ]
Tawa, Akio [11 ]
Horibe, Keizo [5 ]
Adachi, Souichi [9 ]
机构
[1] St Marianna Univ Sch Med, Dept Paediat, Kawasaki, Kanagawa 2168511, Japan
[2] Tokai Univ Sch Med, Dept Lab Med, Isehara, Kanagawa, Japan
[3] Kyoto Prefectural Univ Med, Dept Mol Diagnost & Therapeut, Kyoto, Japan
[4] Aichi Gakuin Univ, Fac Psychol Sci, Dept Nutr & Hlth, Nagoya, Aichi, Japan
[5] Natl Hosp Org, Clin Res Ctr, Nagoya, Aichi, Japan
[6] Tokyo Med & Dent Univ, Dept Paediat, Tokyo, Japan
[7] Shiga Univ Med Sci, Dept Paediat, Otsu, Shiga 52021, Japan
[8] Toho Univ, Dept Paediat, Tokyo, Japan
[9] Kyoto Univ, Kyoto, Japan
[10] Gunma Childrens Med Ctr, Dept Haematol Oncol, Gunma, Japan
[11] Natl Hosp Org, Osaka Med Ctr, Dept Paediat, Osaka, Japan
关键词
paediatric acute myeloid leukaemia; WHO classification; multilineage dysplasia; myelodysplasia; INDEPENDENT PROGNOSTIC RELEVANCE; WORLD-HEALTH-ORGANIZATION; DE-NOVO AML; MULTILINEAGE DYSPLASIA; TRILINEAGE DYSPLASIA; CLASSIFICATION; CRITERIA; OUTCOMES;
D O I
10.1111/bjh.12993
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The clinical characteristics and prognostic relevance of acute myeloid leukaemia (AML) with myelodysplastic features remains to be clarified in children. We prospectively examined 443 newly diagnosed patients in a multicentre clinical trial for paediatric de novo AML, and found AML with myelodysplasia-related changes' (AML-MRC) according to the 2008 World Health Organization classification in 93 (210%), in whom 59 were diagnosed from myelodysplasia-related cytogenetics alone, 28 from multilineage dysplasia alone and six from a combination of both. Compared with 111 patients with AML, not otherwise specified' (AML-NOS), patients with AML-MRC' presented at a younger age, with a lower white blood cell count, higher incidence of 20-30% bone marrow blasts, unfavourable cytogenetics and a lower frequency of Fms-like tyrosine kinase 3 internal tandem duplication (FLT3-ITD), NPM1 and CEBPA mutations. Complete remission rate and 3-year probability of event-free survival were significantly worse in AML-MRC' patients (677 vs. 856%, P<001, 371% vs. 538%, P=002, respectively), but 3-year overall survival and relapse-free survival were comparable with AML-NOS' patients. By multivariate analysis, FLT3-ITD was solely associated with worse overall survival. These results support the distinctive features of the category AML-MRC' even in children.
引用
收藏
页码:80 / 86
页数:7
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