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Updated: May 13, 2026

Therapy Testing in a Spheroid-based 3D Cell Culture Model for Head and Neck Squamous Cell Carcinoma
Published on: April 20, 2018
Personalized therapy on the horizon for squamous cell carcinoma of the lung
Han Sang Kim1, Tetsuya Mitsudomi, Ross A Soo
1Division of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Abstract:
Squamous cell carcinoma (SQCC) of the lung is the second-largest subtype of non-small cell lung cancer (NSCLC), causing an estimated 400,000 deaths per year worldwide. Recent developments in cancer genome sequencing technology expanded our knowledge of driver mutations, which were identified as novel candidates for targeted therapy in various cancers. Successful targeted treatments for lung adenocarcinoma, NSCLC's primary subtype, with EGFR mutation or ALK fusion are clinically available, and a clinical trial of personalized targeted therapy in patients with lung adenocarcinoma is underway by the Lung Cancer Mutation Consortium. Although there are targeted treatments for lung adenocarcinoma, no personalized therapies currently exist for SQCC. Recently, comprehensive genomic characterization of lung SQCC using massively parallel sequencing has enabled us to identify several potential driver mutations/signaling pathways. These are FGFR1 amplifications, PI3KCA mutations, PTEN mutations/deletions, PDGFRA amplifications/mutations, and DDR2 mutations. The march toward personalized therapy may have taken a step forward with the discovery of these potential biomarkers for the treatment of SQCC of the lung. This article reviewed the current knowledge of genomic landscape of lung SQCC and summarized ongoing clinical trials of targeted agents for lung SQCC. Also, we will suggest several other actionable mutations with matching drugs that should be investigated in future clinical trials for the personalized treatment of lung SQCC.
Insights
Lung squamous cell carcinoma (SQCC) lacks targeted therapies, unlike lung adenocarcinoma. Genomic sequencing identified new potential biomarkers like FGFR1 amplifications and PI3KCA mutations for personalized SQCC treatment.
Area of Science:
- Oncology
- Genomics
- Translational Medicine
Background:
- Lung squamous cell carcinoma (SQCC) is a major cause of cancer death, representing the second-largest subtype of non-small cell lung cancer (NSCLC).
- Existing targeted therapies for NSCLC primarily benefit lung adenocarcinoma, leaving a significant unmet need for SQCC treatment.
- Advances in cancer genome sequencing have revealed potential therapeutic targets in various cancers.
Purpose of the Study:
- To review the current genomic landscape of lung SQCC.
- To summarize ongoing clinical trials for targeted agents in lung SQCC.
- To identify and suggest novel actionable mutations for future personalized SQCC therapies.
Main Methods:
- Comprehensive genomic characterization of lung SQCC using massively parallel sequencing.
- Review of current literature on lung SQCC genomic alterations.
- Analysis of ongoing clinical trials for targeted agents in lung SQCC.
Main Results:
- Identification of potential driver mutations and signaling pathways in lung SQCC, including FGFR1 amplifications, PI3KCA mutations, PTEN mutations/deletions, PDGFRA amplifications/mutations, and DDR2 mutations.
- Highlighting the disparity in targeted therapy availability between lung adenocarcinoma and SQCC.
- Establishing a foundation for personalized medicine in lung SQCC.
Conclusions:
- Genomic discoveries offer new hope for developing targeted therapies for lung SQCC.
- Further investigation of identified biomarkers and novel actionable mutations is crucial for advancing personalized treatment strategies.
- The findings pave the way for future clinical trials aimed at improving outcomes for lung SQCC patients.
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