DNA methylation holds prognostic information in relapsed precursor B-cell acute lymphoblastic leukemia

被引:17
作者
Borssen, Magnus [1 ]
Nordlund, Jessica [2 ,3 ]
Haider, Zahra [1 ]
Landfors, Mattias [1 ]
Larsson, Par [1 ]
Kanerva, Jukka [4 ]
Schmiegelow, Kjeld [5 ,6 ]
Flaegstad, Trond [7 ,8 ]
Jonsson, Olafur Gisli [9 ]
Frost, Britt-Marie [10 ]
Palle, Josefine [10 ]
Forestier, Erik [1 ]
Heyman, Mats [11 ]
Hultdin, Magnus [1 ]
Lonnerholm, Gudmar [10 ]
Degerman, Sofie [1 ]
机构
[1] Umea Univ, Dept Med Biosci, Blg 6M,2nd Floor, SE-90185 Umea, Sweden
[2] Uppsala Univ, Dept Med Sci, Uppsala, Sweden
[3] Uppsala Univ, Sci Life Lab, Uppsala, Sweden
[4] Univ Helsinki, Cent Hosp, Childrens Hosp, Helsinki, Finland
[5] Univ Copenhagen, Rigshosp, Dept Paediat & Adolescent Med, Copenhagen, Denmark
[6] Univ Copenhagen, Inst Clin Med, Copenhagen, Denmark
[7] Univ Tromso, Dept Pediat, Tromso, Norway
[8] Univ Hosp North Norway, Tromso, Norway
[9] Landspitali Univ Hosp, Childrens Hosp, Pediat Hematol Oncol, Reykjavik, Iceland
[10] Uppsala Univ, Dept Womens & Childrens Hlth, Pediat, Uppsala, Sweden
[11] Karolinska Univ Hosp, Karolinska Inst, Dept Womens & Childrens Hlth, Childhood Canc Res Unit, Stockholm, Sweden
来源
CLINICAL EPIGENETICS | 2018年 / 10卷
基金
瑞典研究理事会;
关键词
DNA methylation; BCP-ALL; Prognosis; CIMP; Relapse; Risk stratification; MINIMAL RESIDUAL DISEASE; LESSONS;
D O I
10.1186/s13148-018-0466-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Few biological markers are associated with survival after relapse of B-cell precursor acute lymphoblastic leukemia (BCP-ALL). In pediatric T-cell ALL, we have identified promoter-associated methylation alterations that correlate with prognosis. Here, the prognostic relevance of CpG island methylation phenotype (CIMP) classification was investigated in pediatric BCP-ALL patients. Methods: Six hundred and one BCP-ALL samples from Nordic pediatric patients (age 1-18) were CIMP classified at initial diagnosis and analyzed in relation to clinical data. Results: Among the 137 patients that later relapsed, patients with a CIMP-profile (n = 42) at initial diagnosis had an inferior overall survival (pOS(5years) 33%) compared to CIMP+ patients (n = 95, pOS(5years) 65%) (p = 0.001), which remained significant in a Cox proportional hazards model including previously defined risk factors. Conclusion: CIMP classification is a strong candidate for improved risk stratification of relapsed BCP-ALL.
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收藏
页数:7
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