Tumor mutation burden and FAT3 mutation influence long-term survival in surgically resected small cell lung cancer.

IF 4 2区 医学 Q2 ONCOLOGY Translational lung cancer research Pub Date : 2024-06-30 Epub Date: 2024-06-27 DOI:10.21037/tlcr-24-467
Xinyu Qian, Lin Zhu, Na Han, Jing Qin
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Abstract

Background: Small cell lung cancer (SCLC) is highly malignant and has a higher risk of recurrence even in patients who undergo early surgery. However, a subgroup of patients survived for many years. So far, the factors that determine the long-term survivorship remain largely unknown. To determine the genetic characteristics of long-term survival (LTS) after surgery in SCLC, we performed comprehensive comparative genomic profiling and tumor mutation burden (TMB) analysis of resected tumor tissues from patients with LTS and short-term survival (STS) after surgery.

Methods: The present study screened 11 patients from 52 patients with SCLC who underwent surgery at Zhejiang Cancer Hospital from April 2008 to December 2017. A total of six LTS patients (≥4 years) with stage IIB or IIIA SCLC and five STS patients (<2 years) with stage IA or IB SCLC were included in the study. The STS patients were used as a control. All the patients underwent resection without neoadjuvant therapy. We assessed the genomic profiles of the resected tumor tissues and calculated the TMB using next-generation sequencing. We then analyzed and compared the molecular characteristics between the LTS and STS groups.

Results: Our data indicated that tumor tissues from patients with LTS harbor a high TMB. The median TMB for LTS patients was high (approximately 16.4 mutations/Mb), while that for STS patients was low (approximately 8.5 mutations/Mb). The median TMB of patients with LTS and STS showed a trend of significant difference (P=0.08). Gene alterations characterized the survival differences between the two groups. The FAT3 mutation was only found in the LTS group, and the P value determined by Fisher's exact test was 0.06.

Conclusions: A high non-synonymous TMB and the FAT3 mutation could potentially influence LTS after SCLC resection. This study provides valuable information about the molecular differences between LTS and STS patients. Studies with larger sample sizes need to be conducted to confirm our findings in the future.

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肿瘤突变负荷和FAT3突变对手术切除小细胞肺癌患者长期生存的影响
背景:小细胞肺癌(SCLC)恶性程度高,即使早期接受手术治疗的患者复发风险也较高。然而,也有一部分患者能存活多年。迄今为止,决定长期存活率的因素在很大程度上仍不为人所知。为了确定SCLC术后长期生存(LTS)的基因特征,我们对术后LTS和短期生存(STS)患者的切除肿瘤组织进行了全面的比较基因组图谱分析和肿瘤突变负荷(TMB)分析:本研究从2008年4月至2017年12月在浙江省肿瘤医院接受手术治疗的52例SCLC患者中筛选出11例患者。其中,ⅡB或ⅢA期SCLC患者共6例LTS(≥4岁),STS患者共5例(结果:我们的数据表明,LTS患者的肿瘤组织蕴藏着较高的TMB。LTS患者的中位TMB较高(约16.4个突变/Mb),而STS患者的中位TMB较低(约8.5个突变/Mb)。LTS和STS患者的中位TMB呈显著差异趋势(P=0.08)。基因改变是两组患者生存差异的特征。FAT3基因突变仅在LTS组中发现,费舍尔精确检验的P值为0.06:结论:高非同义TMB和FAT3突变可能会影响SCLC切除术后的LTS。这项研究为 LTS 和 STS 患者的分子差异提供了有价值的信息。未来需要进行样本量更大的研究来证实我们的发现。
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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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