Sefrioui David, Blanchard France, Toure Emmanuel, Basile Paul, Beaussire Ludivine, Dolfus Claire, Perdrix Anne, Paresy Marianne, Antonietti Michel, Iwanicki-Caron Isabelle, Alhameedi Raied, Lecleire Stephane, Gangloff Alice, Schwarz Lilian, Clatot Florian, Tuech Jean-Jacques, Frébourg Thierry, Jardin Fabrice, Sabourin Jean-Christophe, Sarafan-Vasseur Nasrin, Michel Pierre, Di Fiore Frédéric
Digestive Oncology Unit, Department of Hepatogastroenterology, Rouen University Hospital, 1 Rue de Germont, Rouen 76031, France.
Normandie University, UNIROUEN, Inserm U1245, Team 3, IRON group, Rouen University Hospital, Normandy Centre for Genomic and Personalized Medicine, F 76000, Rouen, France.
Br J Cancer. 2017 Sep 26;117(7):1017-1025. doi: 10.1038/bjc.2017.250. Epub 2017 Aug 3.
The direct comparison of CA19.9, circulating tumour cells (CTCs) and circulating tumour DNA (ctDNA) using endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) has never been performed for the diagnosis of solid pancreatic tumours (SPTs).
We included 68 patients with a SPT referred for EUS-FNA. CTCs were analysed using size-based platform and ctDNA using digital PCR. The sensitivity, specificity, negative and positive predictive values were evaluated for each marker and their combination.
SPTs corresponded to 58 malignant tumours (52 pancreatic adenocarcinoma (PA) and 6 others) and 10 benign lesions. The sensitivity and specificity for PA diagnosis were 73% and 88% for EUS-FNA, 67% and 80% for CTC, 65% and 75% for ctDNA and 79% and 93% for CA19.9, respectively. The positivity of at least 2 markers was associated with a sensitivity and specificity of 78% and 91%, respectively. CtDNA was the only marker associated with overall survival (median 5.2 months for ctDNA+ vs 11.0 months for ctDNA-, P=0.01).
CA19.9 alone and in combination with ctDNA and/or CTC analysis may represent an efficient method for diagnosing PA in patients with SPTs. Further studies including a larger cohort of patients with both malignant and benign lesions will be necessary to confirm these promising results.
从未采用内镜超声引导下细针穿刺活检(EUS-FNA)对糖类抗原19-9(CA19.9)、循环肿瘤细胞(CTC)和循环肿瘤DNA(ctDNA)进行直接比较,以诊断实性胰腺肿瘤(SPT)。
我们纳入了68例因EUS-FNA前来就诊的SPT患者。使用基于大小的平台分析CTC,使用数字PCR分析ctDNA。对每个标志物及其组合的敏感性、特异性、阴性和阳性预测值进行评估。
SPT包括58例恶性肿瘤(52例胰腺腺癌(PA)和6例其他肿瘤)和10例良性病变。EUS-FNA诊断PA的敏感性和特异性分别为73%和88%,CTC分别为67%和80%,ctDNA分别为65%和75%,CA19.9分别为79%和93%。至少2种标志物呈阳性与敏感性78%和特异性91%相关。CtDNA是唯一与总生存期相关的标志物(ctDNA阳性组的中位生存期为5.2个月,ctDNA阴性组为11.0个月,P=0.01)。
单独使用CA19.9以及联合ctDNA和/或CTC分析可能是诊断SPT患者PA的有效方法。需要进一步开展研究,纳入更多伴有恶性和良性病变的患者队列,以证实这些有前景的结果。