Publication:
What would next generation sequencing bring to the diagnosis and treatment of sarcomas? a series of 20 cases, a single institution's experience

dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorBulutay, Pınar
dc.contributor.kuauthorKulaç, İbrahim
dc.contributor.kuauthorMeriçöz, Çisel Aydın
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T12:15:00Z
dc.date.issued2021
dc.description.abstractObjective: soft tissue tumors comprise a small proportion of a pathologist's routine practice. Although morphology and immunohistochemistry are quite helpful for diagnosing these tumors, many require molecular tests. Fluorescence in-situ hybridization has been the most commonly used method for the detection of specific genomic alteration, but next generation sequencing (NGS) could be more informative in many ways. Here we present our targeted NGS experience on soft tissue tumors with a series of 20 cases. Material and method: the Laboratory Information System (LIS) was screened for soft tissue tumors that had been sequenced by NGS (between January 2018 - February 2021). 20 consecutive cases were included in the study. All cases were sequenced using a commercial targeted sequencing panel designed for soft tissue tumors. Results: we were able to run a reliable sequencing study for 16 (80%) of the cases but 4 (20%) of them failed in quality tests. We have found pathogenic alterations in 12 (60%) of the cases. The most common alterations were EWSR1 fusions, FLI1 being the most common partner. NGS results drastically changed the initial diagnosis, and thus the treatment modalities, in 3 cases (15%): the case with ETV6-NTRK3 fusion, the case with FUS-TFCP2 fusion, and the case of rhabdomyosarcoma (RMS) that was favored to be of the alveolar subtype and turned out to lack FOXO1 fusions. Conclusion: a targeted NGS panel is robust and very informative. It not only allows pathologists to further specify and/or confirm their diagnosis but it could also play an important role in predicting the outcome.
dc.description.fulltextYES
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue3
dc.description.openaccessYES
dc.description.publisherscopeNational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipN/A
dc.description.versionPublisher version
dc.description.volume37
dc.identifier.doi10.5146/tjpath.2021.01544
dc.identifier.eissn1309-5730
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR03213
dc.identifier.issn1018-5615
dc.identifier.quartileN/A
dc.identifier.scopus2-s2.0-85115079788
dc.identifier.urihttps://hdl.handle.net/20.500.14288/1320
dc.identifier.wos695696200010
dc.keywordsSarcoma
dc.keywordsSoft tissue tumors
dc.keywordsNext generation sequencing
dc.keywordsMolecular pathology
dc.language.isoeng
dc.publisherBuluş Design
dc.relation.grantnoNA
dc.relation.ispartofTurkish Journal of Pathology / Türk Patoloji Dergisi
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/9987
dc.subjectPathology
dc.titleWhat would next generation sequencing bring to the diagnosis and treatment of sarcomas? a series of 20 cases, a single institution's experience
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorKulaç, İbrahim
local.contributor.kuauthorBulutay, Pınar
local.contributor.kuauthorMeriçöz, Çisel Aydın
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
9987.pdf
Size:
1.1 MB
Format:
Adobe Portable Document Format