| Literature DB >> 33903952 |
Anna Hecht1, Julia A Meyer2, Johann-Christoph Jann3, Katja Sockel4, Aristoteles Giagounidis5, Katharina S Götze6, Anne Letsch7, Detlef Haase8, Richard F Schlenk9, Torsten Haferlach10, Philippe Schafhausen11, Gesine Bug12, Michael Lübbert13, Felicitas Thol14, Guntram Büsche15, Esther Schuler16, Verena Nowak3, Julia Obländer3, Stephanie Fey3, Nadine Müller3, Georgia Metzgeroth3, Wolf-Karsten Hofmann3, Ulrich Germing16, Florian Nolte3, Mark Reinwald17, Daniel Nowak3.
Abstract
Myelodysplastic syndrome (MDS) with isolated deletion of chromosome 5q (MDS del5q) is a distinct subtype of MDS with quite favorable prognosis and excellent response to treatment with lenalidomide. Still, a relevant percentage of patients do not respond to lenalidomide and even experience progression to acute myeloid leukemia (AML). In this study, we aimed to investigate whether global DNA methylation patterns could predict response to lenalidomide. Genome-wide DNA methylation analysis using Illumina 450k methylation arrays was performed on n=51 patients with MDS del5q who were uniformly treated with lenalidomide in a prospective multicenter trial of the German MDS study group. To study potential direct effects of lenalidomide on DNA methylation, 17 paired samples pre- and post-treatment were analyzed. Our results revealed no relevant effect of lenalidomide on methylation status. Furthermore, methylation patterns prior to therapy could not predict lenalidomide response. However, methylation clustering identified a group of patients with a trend towards inferior overall survival. These patients showed hypermethylation of several interesting target genes, including genes of relevant signaling pathways, potentially indicating the evaluation of novel therapeutic targets.Entities:
Keywords: DNA methylation; Deletion 5q; Lenalidomide; Myelodysplastic syndromes
Year: 2021 PMID: 33903952 DOI: 10.1007/s00277-021-04492-1
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673