| Literature DB >> 35167654 |
Yassmine M N Akkari1, Linda B Baughn2, Adrian M Dubuc3, Adam C Smith4, Mar Mallo5, Paola Dal Cin3, Maria Diez Campelo6, Marta S Gallego7, Isabel Granada Font8, Detlef T Haase9, Brigitte Schlegelberger10, Irma Slavutsky11, Cristina Mecucci12, Ross L Levine13, Robert P Hasserjian14, Francesc Solé5, Brynn Levy15, Xinjie Xu2.
Abstract
Cytogenetics has long represented a critical component in the clinical evaluation of hematologic malignancies. Chromosome banding studies provide a simultaneous snapshot of genome-wide copy number and structural variation, which have been shown to drive tumorigenesis, define diseases, and guide treatment. Technological innovations in sequencing have ushered in our present-day clinical genomics era. With recent publications highlighting novel sequencing technologies as alternatives to conventional cytogenetic approaches, we, an international consortium of laboratory geneticists, pathologists, and oncologists, describe herein the advantages and limitations of both conventional chromosome banding and novel sequencing technologies and share our considerations on crucial next steps to implement these novel technologies in the global clinical setting for a more accurate cytogenetic evaluation, which may provide improved diagnosis and treatment management. Considering the clinical, logistic, technical, and financial implications, we provide points to consider for the global evolution of cytogenetic testing.Entities:
Mesh:
Year: 2022 PMID: 35167654 DOI: 10.1182/blood.2021014309
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113