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Insights into treatment-specific prognostic somatic mutations in NSCLC from the AACR NSCLC GENIE BPC cohort analysis.
Liu, Yi; Yalavarthi, Sindhu; Yang, Fan; Abdul-Rashid, Yusif; Tang, Shenkun; Long, Zihe; Qin, Yongkai; Wu, Kerui; Wang, Zhifei.
Affiliation
  • Liu Y; Department of Neurosurgery, the Third XiangYa Hospital of Central South University, Changsha, 410013, PR China.
  • Yalavarthi S; Department of Nanoscience, The Joint School of Nanoscience and Nanoengineering, University of North Carolina Greensboro, Greensboro, NC, 27401, USA.
  • Yang F; Department of Neurosurgery, the Third XiangYa Hospital of Central South University, Changsha, 410013, PR China.
  • Abdul-Rashid Y; Department of Nanoscience, The Joint School of Nanoscience and Nanoengineering, University of North Carolina Greensboro, Greensboro, NC, 27401, USA.
  • Tang S; Department of Neurosurgery, the Third XiangYa Hospital of Central South University, Changsha, 410013, PR China.
  • Long Z; Department of Neurosurgery, the Third XiangYa Hospital of Central South University, Changsha, 410013, PR China.
  • Qin Y; Department of Neurosurgery, the Third XiangYa Hospital of Central South University, Changsha, 410013, PR China.
  • Wu K; Department of Nanoscience, The Joint School of Nanoscience and Nanoengineering, University of North Carolina Greensboro, Greensboro, NC, 27401, USA.
  • Wang Z; Department of Neurosurgery, the Third XiangYa Hospital of Central South University, Changsha, 410013, PR China. doctorwangzhifei@163.com.
BMC Pulm Med ; 24(1): 309, 2024 Jul 02.
Article in En | MEDLINE | ID: mdl-38956553
ABSTRACT

BACKGROUND:

Treatment of non-small lung cancer (NSCLC) has evolved in recent years, benefiting from advances in immunotherapy and targeted therapy. However, limited biomarkers exist to assist clinicians and patients in selecting the most effective, personalized treatment strategies. Targeted next-generation sequencing-based genomic profiling has become routine in cancer treatment and generated crucial clinicogenomic data over the last decade. This has made the development of mutational biomarkers for drug response possible.

METHODS:

To investigate the association between a patient's responses to a specific somatic mutation treatment, we analyzed the NSCLC GENIE BPC cohort, which includes 2,004 tumor samples from 1,846 patients.

RESULTS:

We identified somatic mutation signatures associated with response to immunotherapy and chemotherapy, including carboplatin-, cisplatin-, pemetrexed- or docetaxel-based chemotherapy. The prediction power of the chemotherapy-associated signature was significantly affected by epidermal growth factor receptor (EGFR) mutation status. Therefore, we developed an EGFR wild-type-specific mutation signature for chemotherapy selection.

CONCLUSION:

Our treatment-specific gene signatures will assist clinicians and patients in selecting from multiple treatment options.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / ErbB Receptors / Lung Neoplasms / Mutation Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: BMC Pulm Med Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / ErbB Receptors / Lung Neoplasms / Mutation Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: BMC Pulm Med Year: 2024 Document type: Article