Publication:
Fusion of old and new: employing touch imprint slides for next generation sequencing in solid tumors

dc.contributor.departmentSchool of Medicine
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentKUISCID (Koç University İşbank Center for Infectious Diseases)
dc.contributor.departmentGraduate School of Health Sciences
dc.contributor.facultymemberYes
dc.contributor.kuauthorEren, Özgür Can
dc.contributor.kuauthorFırat, Pınar Arıkan
dc.contributor.kuauthorKulaç, İbrahim
dc.contributor.kuauthorMeriçöz, Çisel Aydın
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.contributor.schoolcollegeinstituteResearch Center
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF HEALTH SCIENCES
dc.date.accessioned2024-12-29T09:37:05Z
dc.date.issued2024
dc.description.abstractBackgroundCytomorphological evaluation of tissue touch imprints during rapid on-site evaluation or intraoperative pathology consultation has crucial value. However, literature on their utility for molecular testing is limited. In this study, we emphasize a further benefit of touch imprint slides and scrutinize our institutional experience on their use in molecular testing, specifically next generation sequencing (NGS).Materials and MethodsNGS-based reports (2019-2023) of Koc University Hospital were retrospectively analyzed and circumstances in which sequencing was conducted on touch imprint slides were retrieved (n = 18). Type/location of the biopsy, diagnosis, results, and quality metrics were recorded.ResultsTouch imprints were addressed when they harbored more neoplastic cells compared with permanent biopsies, when suboptimal fixation mitigated deoxyribonucleic acid/ribonucleic acid (DNA/RNA) yield in resections or when the sample was obtained from bone and required decalcification. Diagnoses were diverse, namely non-small-cell lung cancer, gastric adenocarcinoma, glial tumor, Ewing sarcoma, and carcinoma of unknown primary. The percentage of tumor cells on slides stretched between 15% and 70%. Molecular findings ranged from KRAS mutations to TRIM1
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessN/A
dc.description.peerreviewstatusPeer-Reviewed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.WoSQuartileQ4
dc.identifier.doi10.1002/dc.25283
dc.identifier.eissn1097-0339
dc.identifier.embargoN/A
dc.identifier.endpage270
dc.identifier.issn8755-1039
dc.identifier.issue5
dc.identifier.pubmed38339821
dc.identifier.scopus2-s2.0-85184917813
dc.identifier.startpage264
dc.identifier.urihttps://doi.org/10.1002/dc.25283
dc.identifier.urihttps://hdl.handle.net/20.500.14288/22262
dc.identifier.volume52
dc.identifier.wos001159763000001
dc.keywordsCytology
dc.keywordsMolecular profiling
dc.keywordsNext generation sequencing
dc.keywordsNGS
dc.keywordsTouch imprint
dc.keywordsTouch preparation
dc.language.isoeng
dc.publisherWiley
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofDiagnostic Cytopathology
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectMedical laboratory technology
dc.subjectPathology
dc.titleFusion of old and new: employing touch imprint slides for next generation sequencing in solid tumors
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorMeriçöz, Çisel Aydın
local.contributor.kuauthorEren, Özgür Can
local.contributor.kuauthorKulaç, İbrahim
local.contributor.kuauthorFırat, Pınar Arıkan
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