| Literature DB >> 27353473 |
Colombe Saillard1, Helene Guermouche2, Coralie Derrieux3, Julie Bruneau4, Laurent Frenzel1, Lucile Couronne1,5, Vahid Asnafi3, Elizabeth Macintyre3, Amélie Trinquand3, Ludovic Lhermitte3, Thierry Molina4, Felipe Suarez1,5, Francois Lemonnier1, Olivier Kosmider2, Richard Delarue1,5, Olivier Hermine1,5, Morgane Cheminant1,5.
Abstract
We report the case of a patient with a history of Epstein-Barr virus-positive large B-cell lymphoma, who relapsed with an angioimmunoblastic T-cell lymphoma (AITL) associated with a chronic myelomonocytic leukaemia (CMML). We performed targeted next-generation sequencing on CMML and AITL DNA, which revealed mutations of TET2, DNMT3A, SRSF2, NRAS and IDH1, thus confirming that the spectrum of AITL mutations share similarities with myeloid disorders. The frequencies of TET2/DNMT3A and SRSF2 variants could support the hypothesis that TET2/DNMT3A mutations occurred in an early progenitor cell, which later progressed to both the AITL and CMML clones. Treatment with 5-azacytidine led to the complete remission of both diseases. Thus, targeting DNA methylation abnormalities in AITL may be an alternative strategy to chemotherapy.Entities:
Keywords: Angioimmunoblastic T-cell lymphoma; DNA methylation; EBV; TET2; azacytidine
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Year: 2016 PMID: 27353473 DOI: 10.1002/hon.2319
Source DB: PubMed Journal: Hematol Oncol ISSN: 0278-0232 Impact factor: 5.271