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Molecular Profile of Advanced Non-Small Cell Lung Cancers in Octogenarians: The Door to Precision Medicine in Elderly Patients

机译:高龄人群晚期非小细胞肺癌的分子概况:老年患者精准医学的大门

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Background: There is a pressing need to expand the evidence base in geriatric lung oncology. Most non-small cell lung cancers (NSCLCs) are diagnosed in the elderly, with approximately 15% of cases affecting octogenarians. Treatment-related decisions are challenging in this population, and the role of biologically driven therapies is still underrated. Methods: A single-institution cohort of 76 NSCLCs from octogenarian patients was submitted to molecular analysis using a next-generation sequencing (NGS) multigene panel, fluorescence in situ hybridization (FISH) analyses, and immunohistochemistry for PD-L1 assessment. Treatment and clinical outcome data were available for 33 patients. Results: Most cases ( n = 66, 87%) harbored at least one genomic alteration. EGFR and KRAS mutations were detected in 18 (24%) and 20 (26%) patients, respectively. No ALK alterations were found, but in two patients ROS1 translocation was identified. Of 22 cases tested, 17 were positive for PD-L1 staining. Octogenarian patients who received tyrosine kinase inhibitors (TKIs) based on molecular analysis showed clinical benefits, with long progression-free survival as expected in TKI-treated younger cohorts. Conclusions: This study highlights the utility of molecular profiling in all advanced-stage NSCLCs, regardless of the age at diagnosis, to drive personalized treatment. The prevalence of druggable alterations and the clinical benefits obtained by biologically-driven therapies in octogenarians were comparable to those of the younger NSCLC population.
机译:背景:迫切需要扩大老年肺肿​​瘤学的证据基础。大多数非小细胞肺癌(NSCLC)都是在老年人中诊断出来的,约有15%的病例影响到八十岁以下人群。在这个人群中,与治疗有关的决定具有挑战性,而生物驱动疗法的作用仍然被低估了。方法:使用下一代测序(NGS)多基因组,荧光原位杂交(FISH)分析和免疫组化PD-L1评估,对来自高龄患者的76例NSCLC的单机构队列进行分子分析。现有33例患者的治疗和临床结局数据。结果:大多数病例(n = 66,87%)具有至少一种基因组改变。分别在18(24%)和20(26%)患者中检测到EGFR和KRAS突变。没有发现ALK改变,但是在两名患者中鉴定出ROS1易位。在测试的22例病例中,有17例PD-L1染色呈阳性。接受基于分子分析的酪氨酸激酶抑制剂(TKI)的八十岁患者显示出临床益处,如TKI治疗的年轻人群预期的那样,无进展生存期较长。结论:这项研究强调了分子谱分析在所有晚期NSCLC中的应用,无论诊断时的年龄如何,都可以推动个性化治疗。在八岁老人中,药物改变的发生率和通过生物驱动疗法获得的临床益处与年轻的NSCLC人群相当。

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