Zhuang Yi-Ping, Wang Hai-Yan, Shi Mei-Qi, Zhang Jin, Feng Yong
Department of Radiology, Jiangsu Cancer Institute and Hospital, Nanjing, China.
Acta Radiol. 2011 Dec 1;52(10):1083-7. doi: 10.1258/ar.2011.110150. Epub 2011 Oct 17.
The safety of using a cutting needle when performing a core-needle biopsy is of major concern, in particular for small lung tumors or tumors near the hilum.
To investigate the usefulness of CT-guided fine needle aspiration biopsy (FNAB) of the lung in obtaining tumor tissue for epidermal growth factor receptor (EGFR) mutation analysis in advanced lung cancer patients.
Forty-three patients with stage IIIB-IV lung cancer were enrolled. In all patients, CT-guided FNAB was performed using an 18-gauge or 20-gauge Chiba aspiration needle for histology diagnosis and EGFR mutation analysis. Complications associated with CT-guided FNAB were observed, and the specimen mutational assessments were recorded.
The obtained tumor samples ranged from 0.5-1.5 cm in length and were adequate for histological and DNA analyses in all patients. No patient had a pneumothorax or hemoptysis. Minor needle tract bleeding appeared in eight patients. Mutation analysis was satisfactorily demonstrated in 23 mutations and 20 non-mutations. Ten and 13 mutations were identified by 18-gauge and 20-gauge needle biopsies, respectively. EFGR mutations, including 12 cases of EGFR exon 19 deletion and 11 cases of exon 21 point mutation, were present in 21 patients with adenocarcinomas, one with squamous cell carcinoma, and one with undifferentiated carcinoma.
CT-guided FNAB is a feasible and safe technique for obtaining lung tumor tissues for EGFR gene mutation analysis.
在进行粗针活检时使用切割针的安全性备受关注,尤其是对于小的肺肿瘤或靠近肺门的肿瘤。
探讨CT引导下肺细针穿刺抽吸活检(FNAB)在获取晚期肺癌患者肿瘤组织以进行表皮生长因子受体(EGFR)突变分析中的实用性。
纳入43例IIIB-IV期肺癌患者。对所有患者使用18号或20号千叶抽吸针进行CT引导下FNAB,以进行组织学诊断和EGFR突变分析。观察与CT引导下FNAB相关的并发症,并记录标本的突变评估情况。
获取的肿瘤样本长度为0.5 - 1.5厘米,所有患者的样本均足以进行组织学和DNA分析。无患者发生气胸或咯血。8例患者出现轻微针道出血。在23例突变和20例非突变中,突变分析结果令人满意。18号和20号针活检分别鉴定出10例和13例突变。21例腺癌、1例鳞状细胞癌和1例未分化癌患者中存在EGFR突变,其中包括12例EGFR外显子19缺失和11例外显子21点突变。
CT引导下FNAB是获取用于EGFR基因突变分析的肺肿瘤组织的一种可行且安全的技术。