Tong L, Ding N, Li J M, Xu X B, Zhang Y, Ye M S, Li C, Zhang X, Hong Q Y, Zhou J, Bai C X, Hu J
Department of Pulmonary Medicine, Zhongshan Hospital, Fudan University, Shanghai Respiratory Research Institute, Shanghai 200032, China.
Zhonghua Jie He He Hu Xi Za Zhi. 2019 Aug 12;42(8):596-601. doi: 10.3760/cma.j.issn.1001-0939.2019.08.007.
To evaluate the feasibility of cell-free tumor DNA in pleural effusion supernatant for assessing the tumor mutational burden (TMB) of advanced lung cancers. From December 2016 to August 2018, 34 lung cancer patients (19 males and 15 females) with pleural effusion were enrolled at Zhongshan Hospital, Fudan University. The median age of the patients was 65 (range, 34-85) years. Before systemic or local antitumor therapy, tumor specific mutations in tumor tissue, pleural effusion supernatant, pleural effusion sediment, and plasma samples from these patients were examined using targeted next-generation sequencing, and TMB levels were calculated respectively. Subgroup analysis was based on smoking history and driver mutation status. Statistical differences were determined using SPSS 16.0 software, and individual groups were compared using the one-way analysis of variance (ANOVA) and LSD- test. The median TMB level of pleural effusion supernatant was 6.23 mutations/Mb, similar to that of tumor tissue (6.23 6.86 mutations/Mb, 1.174, 0.245), but significantly higher than that of pleural effusion sediment (2.49 mutations/Mb, 3.044, 0.003) and plasma (2.49 mutations/Mb, 2.464, 0.016). Compared with tumor tissue in TMB assessment, pleural effusion supernatant had a positive percentage agreement of 52% (9/17), and a negative percentage agreement of 65% (11/17). Subgroup analysis showed that the TMB level was higher in smokers (11) than that in non-smokers (23, 14.4 5.4 mutations/Mb, 3.238, 0.003). For advanced lung cancer patients with pleural effusion, pleural effusion supernatant is a promising substitute to tumor tissue for TMB assessment, which is a potential biomarker for immunotherapy.
评估胸腔积液上清液中游离肿瘤DNA用于评估晚期肺癌肿瘤突变负荷(TMB)的可行性。2016年12月至2018年8月,复旦大学附属中山医院招募了34例伴有胸腔积液的肺癌患者(男性19例,女性15例)。患者的中位年龄为65岁(范围34 - 85岁)。在进行全身或局部抗肿瘤治疗前,使用靶向二代测序检测这些患者肿瘤组织、胸腔积液上清液、胸腔积液沉淀物及血浆样本中的肿瘤特异性突变,并分别计算TMB水平。亚组分析基于吸烟史和驱动基因突变状态。使用SPSS 16.0软件确定统计学差异,各分组间比较采用单因素方差分析(ANOVA)和LSD检验。胸腔积液上清液的中位TMB水平为6.23个突变/Mb,与肿瘤组织的水平相似(6.23±6.86个突变/Mb,t = 1.174,P = 0.245),但显著高于胸腔积液沉淀物(2.49个突变/Mb,t = 3.044,P = 0.003)和血浆(2.49个突变/Mb,t = 2.464,P = 0.016)。在TMB评估中,与肿瘤组织相比,胸腔积液上清液的阳性百分比一致性为52%(9/17),阴性百分比一致性为65%(11/17)。亚组分析显示,吸烟者(11例)的TMB水平高于非吸烟者(23例,14.4±5.4个突变/Mb,t = 3.238,P = 0.003)。对于伴有胸腔积液的晚期肺癌患者,胸腔积液上清液是用于TMB评估的一种有前景的替代肿瘤组织的样本,TMB是免疫治疗的潜在生物标志物。