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印度尼西亚肺腺癌中罕见突变的谱系:对4778例病例进行8年分析的结果凸显了对先进靶向治疗的需求。

Spectrum of rare mutations in Indonesian lung adenocarcinoma: Findings from an 8-year analysis of 4,778 cases highlighting the need for advanced targeted therapies.

作者信息

Heriyanto Didik S, Trisnawati Ika, Rachmadi Lisnawati, Tenggara Jeffry B, Lau Vincent, Gunawan Andrew N, Halim Brigitta N, Yuliani Fara S, Laiman Vincent, Gondhowiardjo Soehartati, Chuang Hsiao-Chi

机构信息

Department of Anatomical Pathology, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.

Department of Anatomical Pathology, Dr. Sardjito Hospital, Yogyakarta, Indonesia.

出版信息

Narra J. 2025 Aug;5(2):e1721. doi: 10.52225/narra.v5i2.1721. Epub 2025 Apr 21.

Abstract

Lung cancer patients in Indonesia exhibit a high prevalence of epidermal growth factor receptor () mutations, with a substantial proportion attributed to rare or uncommon variants. The clinical significance of rare mutations lies in their differential sensitivity to tyrosine kinase inhibitors (TKIs). While they are frequently resistant to first- and second-generation TKIs, they often respond to third-generation TKIs, necessitating tailored treatment options. The need for improving access to advanced targeted therapies in Indonesia also highlights the importance of conducting research on rare mutations. The aim of this study was to identify the spectrum and frequency of mutations in patients with lung adenocarcinoma in Indonesia. A cross-sectional observational study with total sampling was conducted from January 2016 to April 2024 to investigate mutation profiles in lung adenocarcinoma patients. Samples were acquired from patients with a confirmed anatomical pathology diagnosis from various healthcare centers across Indonesia. A total of 4,778 samples were analyzed using real-time quantitative polymerase chain reaction (RT-qPCR) on various specimen types to determine mutation prevalence and patterns. Associations between demographic data and mutation status were assessed. mutations were detected in 54.6% of samples, with common mutations (exon 19 deletions/insertions and point mutation L858R) comprising 76.2% of positive cases and rare mutations (exon 20 insertions, point mutation G719X, S768I, T790M, and L861Q) accounted for 20.3%. Significant associations were found between geographic origin, age, and sex with mutation status. This study confirms substantial genetic variability and geographical differences in mutations among Indonesian lung adenocarcinoma patients, emphasizing the urgent need for further research to prompt enhanced molecular diagnostics and targeted therapies in the region.

摘要

印度尼西亚的肺癌患者中表皮生长因子受体()突变的患病率很高,其中很大一部分归因于罕见或不常见的变异。罕见 突变的临床意义在于它们对酪氨酸激酶抑制剂(TKIs)的敏感性不同。虽然它们通常对第一代和第二代TKIs耐药,但它们常常对第三代TKIs有反应,因此需要量身定制治疗方案。在印度尼西亚,改善获得先进靶向治疗的需求也凸显了对罕见 突变进行研究的重要性。本研究的目的是确定印度尼西亚肺腺癌患者中 突变的谱和频率。2016年1月至2024年4月进行了一项采用全样本的横断面观察性研究,以调查肺腺癌患者的 突变谱。样本取自印度尼西亚各地不同医疗中心经解剖病理学确诊的患者。使用实时定量聚合酶链反应(RT-qPCR)对总共4778个样本的各种标本类型进行分析,以确定 突变的患病率和模式。评估了人口统计学数据与 突变状态之间的关联。在54.6%的样本中检测到 突变,常见突变(外显子19缺失/插入和点突变L858R)占阳性病例的76.2%,罕见突变(外显子20插入、点突变G719X、S768I、T790M和L861Q)占20.3%。发现地理来源、年龄和性别与 突变状态之间存在显著关联。本研究证实了印度尼西亚肺腺癌患者中 突变存在大量遗传变异性和地理差异,强调迫切需要进一步研究,以促进该地区分子诊断和靶向治疗的改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1bd/12425551/9b96fb45ee59/NarraJ-5-e1721-g001.jpg

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