Thoracic Cancer Service, Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Thoracic Cancer Service, Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
J Thorac Oncol. 2017 Feb;12(2):258-268. doi: 10.1016/j.jtho.2016.10.021. Epub 2016 Nov 16.
Targeted therapy significantly prolongs survival in lung adenocarcinoma. Current diagnostic guidelines include only EGFR and anaplastic lymphoma receptor tyrosine kinase gene (ALK) testing. Next-generation sequencing (NGS) reveals more actionable genomic alterations than do standard diagnostic methods. Data on the influence of hybrid capture (HC)-based NGS on treatment are limited, and we investigated its impact on treatment decisions and clinical outcomes.
This retrospective study included patients with advanced lung cancer on whom HC-based NGS was performed between November 2011 and October 2015. Demographic and clinicopathologic characteristics, treatments, and outcome data were collected.
A total of 101 patients were included (median age 63 years [53% females, 45% never-smokers, and 85% with adenocarcinoma]). HC-based NGS was performed upfront and after EGFR/ALK testing yielded negative or inconclusive results in 15% and 85% of patients, respectively. In 51.5% of patients, HC-based NGS was performed before first-line therapy, and in 48.5%, it was performed after treatment failure. HC-based NGS identified clinically actionable genomic alterations in 50% of patients, most frequently in EGFR (18%), Ret proto-oncogene (RET) (9%), ALK (8%), Mesenchymal-epithelial transition factor (MET) receptor tyrosine kinase gene (6%), and erb-b2 receptor tyrosine kinase 2 gene (ERBB2) (5%). In 15 patients, it identified EGFR/ALK aberrations after negative results of prior standard testing. Treatment strategy was changed for 43 patients (42.6%). The overall response rate in these patients was 65% (complete response 14.7%, partial response 50%). Median survival was not reached. Immunotherapy was administered in 33 patients, mostly without an actionable driver, with a presenting disease control rate of 32%, and with an association with tumor mutation burden.
HC-based NGS influenced treatment decisions in close to half of the patients with lung adenocarcinoma and was associated with an overall response rate of 65%, which may translate into a survival benefit.
靶向治疗显著延长了肺腺癌患者的生存期。目前的诊断指南仅包括 EGFR 和间变性淋巴瘤受体酪氨酸激酶基因(ALK)检测。下一代测序(NGS)比标准诊断方法揭示更多可操作的基因组改变。关于杂交捕获(HC)-NGS 对治疗影响的数据有限,我们研究了其对治疗决策和临床结果的影响。
这项回顾性研究纳入了 2011 年 11 月至 2015 年 10 月间接受 HC-NGS 检测的晚期肺癌患者。收集了人口统计学和临床病理学特征、治疗和结局数据。
共纳入 101 例患者(中位年龄 63 岁[53%为女性,45%为从不吸烟者,85%为腺癌])。HC-NGS 分别在 EGFR/ALK 检测阴性或不确定的情况下,在 15%和 85%的患者中进行了初始和后续检测。在 51.5%的患者中,HC-NGS 在一线治疗前进行,在 48.5%的患者中,在治疗失败后进行。HC-NGS 在 50%的患者中发现了具有临床意义的基因组改变,最常见的是 EGFR(18%)、Ret 原癌基因(RET)(9%)、ALK(8%)、间质-上皮转化因子(MET)受体酪氨酸激酶基因(6%)和 erb-b2 受体酪氨酸激酶 2 基因(ERBB2)(5%)。在 15 例患者中,它在先前标准检测阴性结果后发现了 EGFR/ALK 异常。43 例患者(42.6%)的治疗策略发生了改变。这些患者的总体缓解率为 65%(完全缓解 14.7%,部分缓解 50%)。中位生存期未达到。33 例患者接受了免疫治疗,大多数患者没有可操作的驱动基因,疾病控制率为 32%,与肿瘤突变负荷有关。
HC-NGS 影响了近一半肺腺癌患者的治疗决策,并与 65%的总体缓解率相关,这可能转化为生存获益。