Legrand Théo, Salleron Julia, Conroy Thierry, Marchal Frédéric, Thomas Jacques, Monard Laure, Biagi James Jim, Lambert Aurélien
Department of Medical Oncology, Institut de Cancérologie de Lorraine, 54500 Vandœuvre-lès-Nancy, France.
Biostatistic Unit, Institut de Cancérologie de Lorraine, 54500 Vandœuvre-lès-Nancy, France.
Cancers (Basel). 2022 Aug 16;14(16):3945. doi: 10.3390/cancers14163945.
The prognosis of pancreatic cancer after curative surgery is burdened by frequent recurrence. The aim of this study was to evaluate the impact of dysplasia in the surgical specimen on disease-free survival (DFS).
A post-hoc analysis of the phase III PRODIGE 24-CCTG PA 6 trial was performed. From April 2012 to October 2016, 493 patients were included in the primary study. Assessment for dysplasia in the surgical specimens was secondarily performed. Dysplasia was defined based on presence and grade of three most common pre-malignant lesions (intraductal papillary mucinous neoplasm (IPMN), mucinous cystic neoplasm (MCN) and pancreatic intraepithelial neoplasia (PanIN). The primary endpoint was DFS validated through multivariate analysis.
Two hundred twenty-six patients (45.9%) had a preneoplastic lesion. PanIN lesions were found in 193 patients (39.2%), including 100 high-grade lesions (20.6%); 43 patients had IPMN lesions (8.7%), including high-grade lesions in 32 (6.5%). Three MCN were described (0.6%). In bivariate analysis, the presence of dysplasia was not associated with poorer DFS (HR = 0.82, 95% CI [0.66; 1.03]). In multivariate analysis, risk factors for poorer DFS were poorly differentiated/undifferentiated tumor, N1 status, R1 surgical margins and perineural invasion.
The presence of dysplasia in the surgical specimen after pancreatic cancer surgery does not worsen DFS.
根治性手术后胰腺癌的预后常因频繁复发而受到影响。本研究旨在评估手术标本中的发育异常对无病生存期(DFS)的影响。
对III期PRODIGE 24-CCTG PA 6试验进行事后分析。2012年4月至2016年10月,493例患者纳入了该初步研究。其次对手术标本中的发育异常进行评估。发育异常是根据三种最常见的癌前病变(导管内乳头状黏液性肿瘤(IPMN)、黏液性囊性肿瘤(MCN)和胰腺上皮内瘤变(PanIN))的存在情况和分级来定义的。主要终点是通过多变量分析验证的DFS。
226例患者(45.9%)有癌前病变。193例患者(39.2%)发现有PanIN病变,其中100例为高级别病变(20.6%);43例患者有IPMN病变(8.7%),其中32例为高级别病变(6.5%)。描述了3例MCN(0.6%)。在二元分析中,发育异常的存在与较差的DFS无关(HR = 0.82,95%CI [0.66;1.03])。在多变量分析中,DFS较差的危险因素是低分化/未分化肿瘤、N1状态、R1手术切缘和神经周围侵犯。
胰腺癌手术后手术标本中存在发育异常并不会使DFS恶化。