Chromothripsis 18 in multiple myeloma patient with rapid extramedullary relapse

Warning

This publication doesn't include Faculty of Economics and Administration. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

SMETANA Jan OPPELT Jan ŠTORK Martin POUR Luděk KUGLÍK Petr

Year of publication 2018
Type Article in Periodical
Magazine / Source MOLECULAR CYTOGENETICS
MU Faculty or unit

Faculty of Science

Citation
Web https://molecularcytogenetics.biomedcentral.com/articles/10.1186/s13039-018-0357-5
Doi http://dx.doi.org/10.1186/s13039-018-0357-5
Keywords Multiple myeloma; Chromothripsis; Array-CGH; NGS; Mutation screening
Description Background Catastrophic chromosomal event known as chromothripsis was proven to be a significant hallmark of poor prognosis in several cancer diseases. While this phenomenon is very rare in among multiple myeloma (MM) patients, its presence in karyotype is associated with very poor prognosis. Case presentation In our case, we report a 62 year female patient with rapid progression of multiple myeloma (MM) into extramedullary disease and short overall survival (OS=23 months). I-FISH investigation revealed presence of gain 1q21 and hyperdiploidy (chromosomes 5,9,15) in 82% and 86%, respectively, while IgH rearrangements, del(17)(p13) and del(13)(q14) were evaluated as negative. Whole-genome profiling using array-CGH showed complex genomic changes including hyperdiploidy (trisomy of chromosomes 3, 5, 9, 11, 15 and 19), monosomy X, structural gains (1q21-1q23.1, 1q32-1q44, 16p13.13-16p11.2) and losses (1q23.1-1q32.1, 8p23.3-8p11.21) of genetic material and chromothripsis in chromosome 18 with 6 breakpoint areas. Next-generation sequencing showed a total of 338 variants with 1.8% (6/338) of pathological mutations in NRAS (c.181C>A, p.Gln61Lys) or variants of unknown significance in TP53, CUX1 and POU4F1. Conclusions Our findings suggest that presence of chromothripsis should be considered as another important genetic hallmark of poor prognosis in MM patients and utilization of genome-wide screening techniques such as array-CGH and NGS improves the clinical diagnostics of the disease.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.