Lung Unit, Royal Marsden Hospital, London, United Kingdom.
Department of Interventional Radiology, Royal Marsden Hospital, London, United Kingdom.
J Thorac Oncol. 2018 Jan;13(1):63-72. doi: 10.1016/j.jtho.2017.09.1958. Epub 2017 Oct 6.
In the era of biomarker-driven systemic therapy for advanced NSCLC, the role of routine repeated biopsies for decision making outside EGFR-mutant disease remains unproven. We report our center's experience of safety and adequacy for molecular retesting of tumor material obtained from image-guided lung rebiopsies in NSCLC.
We performed a retrospective case note analysis of patients undergoing image-guided lung rebiopsies at a single cancer center between 2011 and 2014. The primary objective was to determine the pathological success rate. Secondary and exploratory objectives were to determine technical success rate, histological concordance, molecular adequacy, genotypes identified, and complication rate.
In all, 103 patients underwent transthoracic image-guided procedures. A total of 66 rebiopsies in NSCLC were identified and analyzed. The pathological success rate was 87.1%. A high histological discordance rate was observed (12 of 52 evaluable cases [23.1%]). Pretest molecular adequacy as determined by the lung pathologist was 78.8% (52 of 66). Of 52 adequate samples 51 were sent for molecular analysis, with a total of 209 genes analyzed (including EGFR, ALK receptor tyrosine kinase gene [ALK], KRAS, BRAF, dicoidin domain receptor tyrosine kinase 2 gene [DDR2], NRAS, ROS1, and rearranged during transfection proto-oncogene gene [RET]). The rate of postgenotyping molecular adequacy was 87.1% (182 of 209). Overall, 20 new potentially actionable mutations were identified, with 13 of 66 patients (19.7%) starting to receive new targeted treatment as a result. Overall, rebiopsies informed clinical decision making in 63.6% of cases. The rates of complications were 15% for pneumothorax, 3% for pneumothorax requiring chest drain, and 8% for hemoptysis.
We have validated the pathological and molecular adequacy rates of rebiopsies and demonstrated clinical utility in routine decision making.
在晚期非小细胞肺癌(NSCLC)的生物标志物驱动的系统治疗时代,针对 EGFR 突变疾病以外的决策进行常规重复活检的作用尚未得到证实。我们报告了本中心在 NSCLC 中对通过图像引导的肺再活检获得的肿瘤组织进行分子重新检测的安全性和充分性的经验。
我们对 2011 年至 2014 年期间在一家癌症中心接受图像引导肺再活检的患者进行了回顾性病历分析。主要目的是确定病理成功率。次要和探索性目标是确定技术成功率、组织学一致性、分子充分性、确定的基因型和并发症发生率。
共有 103 例患者接受了经胸图像引导程序。总共确定并分析了 66 例 NSCLC 再活检。病理成功率为 87.1%。观察到高的组织学不一致率(52 例可评估病例中有 12 例[23.1%])。术前由肺病理学家确定的分子充分性为 78.8%(66 例中的 52 例)。在 52 例充足的样本中,51 例被送进行分子分析,共分析了 209 个基因(包括 EGFR、ALK 受体酪氨酸激酶基因[ALK]、KRAS、BRAF、二聚化域受体酪氨酸激酶 2 基因[DDR2]、NRAS、ROS1 和转位重排原癌基因[RET])。基因分型后的分子充分率为 87.1%(209 个中的 182 个)。总的来说,确定了 20 个新的潜在可治疗突变,结果有 66 例患者中的 13 例(19.7%)开始接受新的靶向治疗。总的来说,再活检在 63.6%的病例中为临床决策提供了信息。气胸的并发症发生率为 15%,需要胸腔引流的气胸为 3%,咯血为 8%。
我们验证了再活检的病理和分子充分率,并证明了其在常规决策中的临床实用性。