Publication: The impact of hybrid capture-based comprehensive genomic profiling on treatment strategies in patients with solid tumors
dc.contributor.coauthor | Dişel, Umut | |
dc.contributor.coauthor | Köse, Fatih | |
dc.contributor.coauthor | Bilici, Ahmet | |
dc.contributor.coauthor | Özgüroğlu, Mustafa | |
dc.contributor.coauthor | Sağlam, Sezer | |
dc.contributor.coauthor | Şeker, Mesut | |
dc.contributor.coauthor | Aksoy, Sercan | |
dc.contributor.coauthor | Tek, İbrahim | |
dc.contributor.coauthor | Mandel, Nil Molinas | |
dc.contributor.coauthor | Demir, Gökhan | |
dc.contributor.coauthor | Arslan, Çağatay | |
dc.contributor.coauthor | Demiray, Mutlu | |
dc.contributor.coauthor | Öztürk, Mehmet Akif | |
dc.contributor.coauthor | Salepçi, Taflan | |
dc.contributor.coauthor | Eralp, Yeşim | |
dc.contributor.coauthor | Temizaş, Gökçe | |
dc.contributor.coauthor | Fidan, Ebru Gül | |
dc.contributor.kuauthor | Selçukbiricik, Fatih | |
dc.contributor.kuprofile | Faculty Member | |
dc.contributor.schoolcollegeinstitute | School of Medicine | |
dc.contributor.yokid | 202015 | |
dc.date.accessioned | 2024-11-09T23:36:52Z | |
dc.date.issued | 2022 | |
dc.description.abstract | Objective: The development of bioinformatics and comprehensive genomic profiling (CGP) has provided insights into the ap-plicability and functionality of the genomic alterations (GA). In this study, we evaluated the impact of CGP on the treatment plan and outcomes in a significant number of patients. Material and Methods: We carried out a retrospective case-control study on 164 adult patients with advanced solid tumors from 15 oncology centers in Türkiye. Results: In all cases, CGP was performed within 23.8 [standard deviation (SD)±32.1] months of initial diagnosis. Non-small cell lung carcinoma, breast cancer, unknown primary carcinoma, colorectal carcinoma, and sarcoma were among the most common tumor types, accounting for 61.5% of all cases. CGP was performed immediately after the diagnosis of advanced cancer in 13 patients (7.9%). In 158 patients (96.4%), at least one GA was found as per the CGP report. Also, in the reports, the average tumor mutational burden (TMB) and GAs were 7.3 (SD±8.7) mut/Mb and 3.5 (SD±2.0), respectively. According to CGP reports, 58 patients had 79 evidence-based drug suggestions for their particular tumor type, whereas 97 patients had 153 evidence-based drug suggestions for another tumor type. After the primary oncologist interpreted the CGP reports, significant changes were made to the treatment of 35 (21.3%) patients. Conclusion: We strongly believe that in the future, high-TMB or other tumor-agnostic biomarkers will become much more afford-able, and CGP will serve as one of the major decision-making tools for the treatment of patients along with pathological, radiological or lab-oratory tests. | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | TR Dizin | |
dc.description.issue | 2 | |
dc.description.openaccess | YES | |
dc.description.publisherscope | National | |
dc.description.volume | 8 | |
dc.identifier.doi | 10.37047/jos.2022-89310 | |
dc.identifier.issn | 2651-4532 | |
dc.identifier.link | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85136777670&doi=10.37047%2fjos.2022-89310&partnerID=40&md5=324ba6a1623626b0d05936e60e3a7f5f | |
dc.identifier.scopus | 2-s2.0-85136777670 | |
dc.identifier.uri | https://dx.doi.org/10.37047/jos.2022-89310 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/12731 | |
dc.keywords | Comprehensive genomic hybridization | |
dc.keywords | Genomics | |
dc.keywords | Neoplasms | |
dc.keywords | Retrospective studies anaplastic lymphoma kinase | |
dc.keywords | Epidermal growth factor receptor | |
dc.keywords | Immunological antineoplastic agent | |
dc.keywords | Adult | |
dc.keywords | Advanced cancer | |
dc.keywords | Article | |
dc.keywords | Breast cancer | |
dc.keywords | Cancer chemotherapy | |
dc.keywords | Cancer immunotherapy | |
dc.keywords | Cancer of unknown primary site | |
dc.keywords | Cancer patient | |
dc.keywords | Case control study | |
dc.keywords | Cohort analysis | |
dc.keywords | Colorectal carcinoma | |
dc.keywords | Controlled study | |
dc.keywords | Female | |
dc.keywords | Fluorescence in situ hybridization | |
dc.keywords | Genomics | |
dc.keywords | Human | |
dc.keywords | Major clinical study | |
dc.keywords | Male | |
dc.keywords | Microsatellite instability | |
dc.keywords | Molecularly targeted therapy | |
dc.keywords | Multicenter study (topic) | |
dc.keywords | Non small cell lung cancer | |
dc.keywords | Observational study | |
dc.keywords | Polymerase chain reaction | |
dc.keywords | Protein fingerprinting | |
dc.keywords | Retrospective study | |
dc.keywords | Sarcoma | |
dc.keywords | Solid malignant neoplasm | |
dc.keywords | Treatment planning | |
dc.keywords | Tumor mutational burden | |
dc.language | English | |
dc.publisher | Türkiye Klinikleri Yayınevi | |
dc.source | Journal of Oncological Sciences | |
dc.subject | Cancer | |
dc.title | The impact of hybrid capture-based comprehensive genomic profiling on treatment strategies in patients with solid tumors | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.authorid | 0000-0002-1273-1674 | |
local.contributor.kuauthor | Selçukbiricik, Fatih |