Kunimasa Kei, Aohara Daisuke, Nishino Kazumi
Department of Thoracic Oncology, Osaka International Cancer Institute, 3-1-69 Otemae Chuoku, Osaka, Osaka, 541-8567, Japan.
Department of Respiratory Medicine, Osaka General Hospital of West Japan Railway Company, Osaka, Japan.
Discov Oncol. 2025 Feb 10;16(1):145. doi: 10.1007/s12672-025-01931-7.
We report a case where a KRAS G12V driver mutation was identified in cerebrospinal fluid (CSF) but not in peripheral blood cell-free DNA (cfDNA) in a patient with advanced lung adenocarcinoma and significant central nervous system involvement. A 67-year-old man presented with hemoptysis and was diagnosed with stage IVB TTF-1-positive lung adenocarcinoma with brain and bone metastases. Standard chemotherapy was ineffective. While cfDNA analysis detected only a RAD21 mutation, CSF analysis revealed the KRAS G12V mutation. Despite the identification, no effective targeted therapy was available. This case highlights that CSF may be more suitable than peripheral blood cfDNA for detecting driver mutations in patients with predominant CNS lesions.
我们报告了一例晚期肺腺癌伴显著中枢神经系统受累患者,其脑脊液(CSF)中检测到KRAS G12V驱动突变,而外周血游离DNA(cfDNA)中未检测到该突变。一名67岁男性因咯血就诊,被诊断为IVB期TTF-1阳性肺腺癌伴脑和骨转移。标准化疗无效。虽然cfDNA分析仅检测到RAD21突变,但CSF分析显示存在KRAS G12V突变。尽管已识别出该突变,但尚无有效的靶向治疗方法。该病例强调,对于以中枢神经系统病变为主的患者,脑脊液可能比外周血cfDNA更适合检测驱动突变。