Case Report: Ensartinib as a first-line treatment for SMARCA4-deficient and EML4-ALK non-small cell lung cancer

SMARC4 is the catalytic subunit of the SWI/SNF chromatin remodeling complex and is one of the most common altered chromatin remodeling ATPases in cancer. Studies have indicated that SMARCA4 loss is associated with highly aggressive tumors, independently predicting shorter overall and disease-specific survival. SMARCA4-deficient non-small cell lung cancer (NSCLC) primarily affects male individuals, especially smokers, and is characterized by large, aggressive tumors. Cases of SMARCA4 deletion combined with actionable driver gene mutations (e.g., ALK) are rarely reported. In this report, we describe a male non-smoker diagnosed with SMARCA4-deficient, <i>EML4-ALK</i> non-small cell lung cancer who has been undergoing ensartinib targeted therapy for 3 months, resulting in a significant partial response. We also propose that, from a signaling perspective, the presence of SMARCA4 deficiency may influence the sensitivity of <i>EML4-ALK</i> NSCLC to targeted therapy, highlighting the need for further investigation into the underlying mechanisms and the exploration of novel therapeutic approaches.

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Publication Details

Journal
Frontiers in Oncology
Published
2025-05-09
DOI
https://doi.org/10.3389/fonc.2025.1530142
Citations
3
Primary Topic
Chromatin Remodeling and Cancer
Type
article
Field-Weighted Citation Impact
2.42

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article

Case Report: Ensartinib as a first-line treatment for SMARCA4-deficient and EML4-ALK non-small cell lung cancer

Shaoxi Wang, Yanqing Pan, Huiling Li, Quanfang Chen et al.
3 citations
Frontiers in Oncology
Chromatin Remodeling and Cancer
2.42
article

Case Report: Ensartinib as a first-line treatment for SMARCA4-deficient and EML4-ALK non-small cell lung cancer

Shaoxi Wang, Yanqing Pan, Huiling Li, Quanfang Chen, Lingxin Yan
article en
3 citations

Abstract

SMARC4 is the catalytic subunit of the SWI/SNF chromatin remodeling complex and is one of the most common altered chromatin remodeling ATPases in cancer. Studies have indicated that SMARCA4 loss is associated with highly aggressive tumors, independently predicting shorter overall and disease-specific survival. SMARCA4-deficient non-small cell lung cancer (NSCLC) primarily affects male individuals, especially smokers, and is characterized by large, aggressive tumors. Cases of SMARCA4 deletion combined with actionable driver gene mutations (e.g., ALK) are rarely reported. In this report, we describe a male non-smoker diagnosed with SMARCA4-deficient, <i>EML4-ALK</i> non-small cell lung cancer who has been undergoing ensartinib targeted therapy for 3 months, resulting in a significant partial response. We also propose that, from a signaling perspective, the presence of SMARCA4 deficiency may influence the sensitivity of <i>EML4-ALK</i> NSCLC to targeted therapy, highlighting the need for further investigation into the underlying mechanisms and the exploration of novel therapeutic approaches.

Frontiers in OncologyVol. 15
Guangxi Medical University (CN), First Affiliated Hospital of GuangXi Medical University (CN)
Natural Science Foundation of Guangxi Province, Wu Jieping Medical Foundation
Good health and well-being
Openalex Percentile: Top 12%
Chromatin Remodeling and Cancer
2.42
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Case Report: Ensartinib as a first-line treatment for SMARCA4-deficient and EML4-ALK non-small cell lung cancer — Shaoxi Wang, Yanqing Pan, et al. · Frontiers in Oncology (2025) | TGRS Research Map | TGRS