Wang Hsin-Yi, Liao Wei-Yu, Ho Chao-Chi, Wu Shang-Gin, Yang Ching-Yao, Hsu Chia-Lin, Lin Yen-Ting, Yang James Chih-Hsin, Shih Jin-Yuan
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, No. 579, Section 2, Yunlin Rd., Yunlin County, Douliu City 640, Taiwan; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, No. 1, Section 4, Roosevelt Rd., Taipei, Taiwan.
Department of Internal Medicine, National Taiwan University Hospital, No. 7, Chung-Shan South Road, Zhongzheng Dist., Taipei City 100, Taiwan.
Eur J Cancer. 2025 Feb 25;217:115224. doi: 10.1016/j.ejca.2025.115224. Epub 2025 Jan 7.
Inadequate tumour samples often hinder molecular testing in non-small cell lung cancer (NSCLC). Plasma-based cell-free DNA (cfDNA) sequencing has shown promise in bypassing these tissue limitations. Nevertheless, pleural effusion (PE) samples may offer a richer cfDNA source for mutation detection in patients with malignant PE.
This prospective study enrolled newly diagnosed advanced NSCLC patients with malignant PE. PE samples were collected for cfDNA NGS analysis. Meanwhile, PE cell pellet RNA was extracted for reverse transcription polymerase chain reaction (RT-PCR) for clinically relevant actionable mutations and then confirmed by Sanger sequencing. The concordance between PE cell pellet RT-PCR and PE cfDNA NGS analyses was analysed.
Fifty patients were enrolled. The median age was 68.5 years, and the female-to-male ratio was 29:21. Most patients (74 %) were non-smokers. Notably, 45/50 patients (90 %) had actionable mutations, including EGFR exon 19 deletions (24 %), EGFR L858R mutations (36 %), HER2 exon20 insertions (10 %), ROS1 rearrangements (4 %), EGFR exon20 insertions (2 %), ALK rearrangements (4 %), RET rearrangements (2 %), KRAS G12C mutations (2 %), and CD74-NRG1 fusions (2 %). Among the 50 enrolled patients, actionable mutations were detected in 44 (88 %) by PE cfDNA NGS, 39 (78 %) by PE cell pellet Sanger sequencing, and 33 (66 %) by clinical tissue genetic testing (P = 0.031). The detection of actionable mutations from PE cfDNA NGS remained consistently high across M1a to M1c stages.
PE cfDNA genotyping has clinical applicability for NSCLC patients and can serve as an additional source for molecular testing. Incorporating PE NGS cfDNA analysis into genetic testing enhances diagnostic yield and aids in identifying actionable mutations in clinical practice.
肿瘤样本不足常常阻碍非小细胞肺癌(NSCLC)的分子检测。基于血浆的游离DNA(cfDNA)测序在克服这些组织限制方面显示出前景。然而,胸腔积液(PE)样本可能为恶性PE患者的突变检测提供更丰富的cfDNA来源。
这项前瞻性研究纳入了新诊断的伴有恶性PE的晚期NSCLC患者。收集PE样本进行cfDNA二代测序(NGS)分析。同时,提取PE细胞沉淀RNA进行逆转录聚合酶链反应(RT-PCR)以检测临床相关的可操作突变,然后通过桑格测序进行确认。分析PE细胞沉淀RT-PCR与PE cfDNA NGS分析之间的一致性。
共纳入50例患者。中位年龄为68.5岁,男女比例为29:21。大多数患者(74%)为非吸烟者。值得注意的是,45/50例患者(90%)存在可操作突变,包括表皮生长因子受体(EGFR)外显子19缺失(24%)、EGFR L858R突变(36%)、人表皮生长因子受体2(HER2)外显子20插入(10%)、ROS1重排(4%)、EGFR外显子20插入(2%)、间变性淋巴瘤激酶(ALK)重排(4%)、转染重排(RET)重排(2%)、 Kirsten大鼠肉瘤病毒癌基因(KRAS)G12C突变(2%)和CD74-NRG1融合(2%)。在50例纳入患者中,通过PE cfDNA NGS检测到44例(88%)可操作突变,通过PE细胞沉淀桑格测序检测到3例9(78%),通过临床组织基因检测检测到33例(66%)(P = 0.031)。从M1a到M1c阶段,PE cfDNA NGS对可操作突变的检测率一直很高。
PE cfDNA基因分型对NSCLC患者具有临床适用性,可作为分子检测的额外来源。将PE NGS cfDNA分析纳入基因检测可提高诊断率,并有助于在临床实践中识别可操作突变。