Clinical implementation of next-generation sequencing testing and genomically-matched therapy: a real-world data in a tertiary hospital
Next-generation sequencing (NGS) cancer profiling has gained traction in routine clinical practice in South Korea. Here, we evaluated the use of NGS testing and genomically-matched therapies for patients with advanced solid tumors in a real-world clinical practice. We analyzed results from NGS cancer panel tests (SNUBH pan-cancer version 2) ordered from June 2019 to June 2020. Genomically-matched treatment was determined based on the novel information obtained from NGS testing, while results from conventional molecular tests were excluded. A total of 990 patients were included in the analysis (median age: 62, Stage IV: 82.5%). Using the Association for Molecular Pathology genetic variant classification system, we found that 257 (26.0%) patients harbored tier I variants, and 859 (86.8%) patients carried tier II variants. Among the tier I cases, the most frequently altered genes we detected were KRAS (106 patients, 10.7%), followed by EGFR (27 patients, 2.7%) and BRAF (17 patients, 1.7%). Of patients with tier I variants, 13.7% received NGS-based therapy as follows: Thyroid cancer (2/7, 28.6%), skin cancer (2/8, 25.0%), gynecologic cancer (7/65, 10.8%), and lung cancer (12/112, 10.7%). Of 32 patients with measurable lesions who received NGS-based therapy, 12 (37.5%) achieved a partial response, and 11 (34.4%) achieved stable disease. The median treatment duration was 6.4 months (95% CI, 4.4-8.4), and the median OS was not reached. In conclusion, NGS tumor profiling was successfully implemented in real-world clinical practice. This enabled the use of molecular profiling-guided therapy which improved survival outcome of selected patients.
Authors
- Soomin Ahn (ORCID: https://orcid.org/0000-0002-1979-4010)
- Hee Young Na (ORCID: https://orcid.org/0000-0002-2464-0665)
- Koung Jin Suh (ORCID: https://orcid.org/0000-0002-1881-8738)
- Gheeyoung Choe (ORCID: https://orcid.org/0000-0001-6547-5603)
- Kihwan Hwang (ORCID: https://orcid.org/0000-0001-7211-729X)
- Yu Jung Kim (ORCID: https://orcid.org/0000-0002-5037-0523)
- Se Hyun Kim (ORCID: https://orcid.org/0000-0002-2292-906X)
- Hye Seung Lee (ORCID: https://orcid.org/0000-0002-1667-7986)
- Kyu Sang Lee (ORCID: https://orcid.org/0000-0003-2801-9072)
- Jaihwan Kim (ORCID: https://orcid.org/0000-0003-0693-1415)
- Jin‐Hyeok Hwang (ORCID: https://orcid.org/0000-0002-5643-8461)
- Chae‐Yong Kim (ORCID: https://orcid.org/0000-0001-9773-5553)
- Keun‐Wook Lee (ORCID: https://orcid.org/0000-0002-8491-703X)
- Hyojin Kim (ORCID: https://orcid.org/0000-0001-9201-8328)
- Ji‐Won Kim (ORCID: https://orcid.org/0000-0001-6426-9074)
- Jee Hyun Kim (ORCID: https://orcid.org/0000-0003-1019-6345)
- Jin Won Kim (ORCID: https://orcid.org/0000-0002-1357-7015)
- So Yeon Park (ORCID: https://orcid.org/0000-0002-0299-7268)
- Jong Seok Lee (ORCID: https://orcid.org/0000-0002-7336-7124)
- Sejoon Lee (ORCID: https://orcid.org/0000-0002-6108-6341)
- Jin Haeng Chung
- Yong Beom Kim
Institutions
- Seoul National University (KR)
- Samsung Medical Center (KR)
- Seoul National University Hospital (KR)
- Seoul National University Bundang Hospital (KR)
- National University College (PR)
Publication Details
- Journal
- Scientific Reports
- Published
- 2025-01-16
- DOI
- https://doi.org/10.1038/s41598-024-84909-9
- Citations
- 13
- Primary Topic
- Genetic factors in colorectal cancer
- Type
- article
- Field-Weighted Citation Impact
- 19.13