Next-generation sequencing-based genomic profiling of advanced soft tissue and bone sarcomas
| dc.contributor.author | Gundogdu, Yasemin | |
| dc.contributor.author | Senocak Tasci, Elif | |
| dc.contributor.author | Ozer, Leyla | |
| dc.contributor.author | Boynukara, Can | |
| dc.contributor.author | Cecen, Recep | |
| dc.contributor.author | Mutlu, Arda Ulas | |
| dc.contributor.author | Yildiz, Ibrahim | |
| dc.date.accessioned | 2026-11-05T11:01:49Z | |
| dc.date.issued | 2025 | |
| dc.description.abstract | Background Sarcomas are rare mesenchymal tumors classified into soft tissue (STS) and bone sarcomas. Despite advances in treatment, the 5-year survival rate for metastatic disease remains low. There is still limited evidence regarding the use of next-generation sequencing (NGS).Aim To identify targetable genomic alterations that may play a crucial role in sarcoma treatment where therapeutic options are limited.Study design Methods: We conducted a retrospective; multicenter analysis of 81 patients diagnosed with STS and bone sarcomas who underwent NGS at Ac & imath;badem Health Group Hospitals to investigate their mutation profiles and explore potential targeted therapies.Results Genomic profiling using four different NGS kits identified a total of 223 genomic alterations across the cohort. Genomic alterations were detectable in 90.1% of patients, with the most common types being copy number amplifications (26.9%) and deletions (24.7%). In addition, actionable mutations were identified in 22.2% of patients, rendering them eligible for FDA-approved targeted therapies. The most common alterations were found in TP53 (38%), RB1 (22%), and CDKN2A (14%) genes. Among the 79 patients with available microsatellite status data, all were microsatellite stable.Conclusion The high proportion of patients eligible for targeted therapies identified underscores the critical need to integrate NGS-derived genetic insights into clinical practice to improve survival rates and treatment outcomes through more tailored therapeutic approaches for each individual. NGS also led to a reclassification of diagnosis in four patients, demonstrating its utility not only in therapeutic decision-making but also as a powerful diagnostic tool. | |
| dc.description.pages | 1627452 | |
| dc.description.volume | 15 | |
| dc.identifier.doi | 10.3389/fonc.2025.1627452 | |
| dc.identifier.issn | 2234-943X | |
| dc.identifier.uri | https://doi.org/10.3389/fonc.2025.1627452 | |
| dc.identifier.uri | https://openaccess.acibadem.edu.tr/handle/11443/10805 | |
| dc.identifier.wos | WOS:001594950100001 | |
| dc.language.iso | en | |
| dc.publisher | FRONTIERS MEDIA SA | |
| dc.relation.hasversion | 10.3389/fonc.2025.1627452 | |
| dc.relation.ispartof | FRONTIERS IN ONCOLOGY | |
| dc.subject | sarcoma | |
| dc.subject | soft tissue | |
| dc.subject | next-generation sequencing | |
| dc.subject | molecular | |
| dc.subject | targeted therapy | |
| dc.subject | Oncology | |
| dc.title | Next-generation sequencing-based genomic profiling of advanced soft tissue and bone sarcomas | |
| dc.type | Article | |
| oaire.citation.edition | Science Citation Index Expanded (SCI-EXPANDED) | |
| oaire.citation.volume | 15 | |
| person.identifier.orcid | 0000-0002-6075-3923 | |
| person.identifier.rid | KBD-3048-2024 | |
| person.identifier.rid | LKJ-8343-2024 |
