RARE CYTOGENETIC ABNORMALITIES IN MYELODYSPLASTIC SYNDROMES

Julie Schanz, Friederike Braulke, Detlef Haase
  • Friederike Braulke
    Affiliation not present
  • Detlef Haase
    Prof. Dr. med. Detlef Haase, MD Clinics of Hematology and Medical Oncology University Medical Center Göttingen Robert-Koch-Str. 40, 37075 Göttingen, Germany Email:Telephone: ++49-0551-39-6313; Telefax: ++49-0551-39-7633, Germany

Abstract

The karyotype represents one of the main cornerstones for the International Prognostic Scoring System (IPSS) and the revised IPSS-R (IPSS-R) that are most widely used for prognostication in patients with myelodysplastic syndromes (MDS). The most frequent cytogenetic abnormalities in MDS, i.e. del(5q), -7/del(7q), +8, complex karyotypes, or –Y have been extensively explored for their prognostic impact. The IPSS-R considers also some less frequent abnormalities such as del(11q), isochromosome 17, +19, or 3q abnormalities. However, more than 600 different cytogenetic categories had been identified in a previous MDS study. This review aims to focus interest on selected rare cytogenetic abnormalities in patients with MDS. Examples are numerical gains of the chromosomes 11 (indicating rapid progression), of chromosome 14 or 14q (prognostically intermediate to favorable), -X (in females, with an intermediate prognosis), or numerical abnormalities of chromosome 21. Structural abnormalities are also considered, e.g. del(13q) that is associated with bone marrow failure syndromes and favorable response to immunosuppressive therapy. These and other rare cytogenetic abnormalities should be integrated into existing prognostication systems such as the IPSS-R. However, due to the very low number of cases, this is clearly dependent on international collaboration. Hopefully, this article will help to inaugurate this process.

Keywords

Myelodysplastic Syndrome, Cytogenetics, Rare Disorders

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Submitted: 2015-03-13 23:40:11
Published: 2015-04-23 00:00:00
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