Rodríguez González Marta, Montero González Juan Carlos, Sayagués Manzano José María, Sánchez Tamara Clavero, Ruiz Jonnathan Roldán, Iglesias Heras Miguel, Rivas Marcos María Belén, Abad Hernández Mar, Cordovilla Pérez Rosa
Department of Pathology, Biomedical Research Institute of Salamanca (IBSAL), University Hospital of Salamanca, 37007 Salamanca, Spain.
Centro de Investigación Biomédica en Red Cáncer (CIBERONC), 28029 Madrid, Spain.
Diagnostics (Basel). 2025 Apr 22;15(9):1064. doi: 10.3390/diagnostics15091064.
: Recent advances in the treatment of non-small cell lung cancer (NSCLC) have shifted from conventional chemotherapy to targeted therapies aimed at specific genetic mutations, particularly in the adenocarcinoma subtype. These therapies have improved overall survival and quality of life. However, some patients still face barriers to accessing these treatments due to challenges in diagnosing advanced-stage NSCLC. Limited tumor cellularity in small biopsies and cytological samples hinders the ability to perform further molecular analyses. Additionally, the increasing number of genetic alterations requiring testing complicates the diagnostic process. To overcome this challenge, we propose combining endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) with next-generation sequencing (NGS) and immunohistochemistry for PD-L1. : A total of 120 EBUS-TBNA samples were consecutively collected during the first year of integrating NGS at a reference hospital in Castilla y León, Spain. Depending on the histology and patient characteristics, a total of 67 NGS analyses and 116 PD-L1 determinations were performed. : The cytological sample obtained in these cases successfully achieved the triple objective proposed by the NCCN for lung cancer (diagnosis, staging, and molecular analysis in a single procedure) in 97% of instances. : Our study highlights the effectiveness of EBUS-TBNA as a comprehensive, cost-effective, and safe diagnostic tool for NSCLC, successfully achieving the triple objective of diagnosis, staging, and molecular analysis in 97% of cases. The procedure consistently provided high-quality samples for NGS and PD-L1 testing, with minimal complications, reinforcing its value as a reliable approach for optimizing personalized treatment strategies.
非小细胞肺癌(NSCLC)治疗的最新进展已从传统化疗转向针对特定基因突变的靶向治疗,尤其是在腺癌亚型中。这些疗法提高了总生存率和生活质量。然而,由于晚期NSCLC诊断方面的挑战,一些患者在获取这些治疗方面仍面临障碍。小活检和细胞学样本中肿瘤细胞数量有限,阻碍了进一步进行分子分析的能力。此外,需要检测的基因改变数量不断增加,使诊断过程变得复杂。为了克服这一挑战,我们建议将支气管内超声引导下经支气管针吸活检(EBUS-TBNA)与下一代测序(NGS)和PD-L1免疫组织化学相结合。
在西班牙卡斯蒂利亚-莱昂的一家参考医院整合NGS的第一年,共连续收集了120份EBUS-TBNA样本。根据组织学和患者特征,共进行了67次NGS分析和116次PD-L1检测。
在这些病例中获得的细胞学样本在97%的情况下成功实现了美国国立综合癌症网络(NCCN)针对肺癌提出的三个目标(在单一操作中进行诊断、分期和分子分析)。
我们的研究强调了EBUS-TBNA作为一种全面、经济高效且安全的NSCLC诊断工具的有效性,在97%的病例中成功实现了诊断、分期和分子分析的三个目标。该操作始终为NGS和PD-L1检测提供高质量样本,并发症极少,强化了其作为优化个性化治疗策略的可靠方法的价值。