Harnessing Institutionally Developed Clinical Targeted Sequencing to Improve Patient Survival in Breast Cancer: A Seven-Year Experience

  • Jiwon Koh
  • , Jinyong Kim
  • , Go Un Woo
  • , Hanbaek Yi
  • , So Yean Kwon
  • , Jeongmin Seo
  • , Jeong Mo Bae
  • , Jung Ho Kim
  • , Jae Kyung Won
  • , Han Suk Ryu
  • , Yoon Kyung Jeon
  • , Dae Won Lee
  • , Miso Kim
  • , Tae Yong Kim
  • , Kyung Hun Lee
  • , Tae You Kim
  • , Jee Soo Lee
  • , Moon Woo Seong
  • , Sheehyun Kim
  • , Sungyoung Lee
  • Hongseok Yun, Myung Geun Song, Jaeyong Choi, Jong Il Kim, Seock Ah Im

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Purpose Considering the high disease burden and unique features of Asian patients with breast cancer (BC), it is essential to have a comprehensive view of genetic characteristics in this population. An institutional targeted sequencing platform was developed through the Korea Research-Driven Hospitals project and was incorporated into clinical practice. This study explores the use of targeted next-generation sequencing (NGS) and its outcomes in patients with advanced/metastatic BC in the real world. Materials and Methods We reviewed the results of NGS tests administered to BC patients using a customized sequencing platform—FiRST Cancer Panel (FCP)—over 7 years. We systematically described clinical translation of FCP for precise diagnostics, personalized therapeutic strategies, and unraveling disease pathogenesis. Results NGS tests were conducted on 548 samples from 522 patients with BC. Ninety-seven point six percentage of tested samples harbored at least one pathogenic alteration. The common alterations included mutations in TP53 (56.2%), PIK3CA (31.2%), GATA3 (13.8%), BRCA2 (10.2%), and amplifications of CCND1 (10.8%), FGF19 (10.0%), and ERBB2 (9.5%). NGS analysis of ERBB2 amplification correlated well with human epidermal growth factor receptor 2 immunohistochemistry and in situ hybridization. RNA panel analyses found potentially actionable and prognostic fusion genes. FCP effectively screened for potentially germline pathogenic/likely pathogenic mutation. Ten point three percent of BC patients received matched therapy guided by NGS, resulting in a significant overall survival advantage (p=0.022), especially for metastatic BCs. Conclusion Clinical NGS provided multifaceted benefits, deepening our understanding of the disease, improving diagnostic precision, and paving the way for targeted therapies. The concrete advantages of FCP highlight the importance of multi-gene testing for BC, especially for metastatic conditions.

Original languageEnglish
Pages (from-to)443-456
Number of pages14
JournalCancer Research and Treatment
Volume57
Issue number2
DOIs
StatePublished - Apr 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Breast neoplasms
  • Cancer evolution
  • Copy number variation
  • Fusion gene
  • Hereditary cancer
  • Mutation
  • Next-generation sequencing
  • Precision diagnosis
  • Precision medicine

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