Institute of Pathology, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
Department of General, Visceral and Cancer Surgery, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
J Cancer Res Clin Oncol. 2023 Aug;149(10):7539-7546. doi: 10.1007/s00432-023-04702-5. Epub 2023 Mar 27.
Rising incidence of pancreatic ductal adenocarcinoma (PDAC) bind with insufficient therapy options showcases a great medical challenge. Further biomarkers are required to identify patients, who will benefit from more aggressive therapy.
320 patients were included by the PANCALYZE study group. Cytokeratin 6 (CK6) immunohistochemical staining as a putative marker for the basal-like subtype of PDAC was performed. The correlation between CK6 expression patterns and survival data, as well as various markers of the (inflammatory) tumor microenvironment, were analyzed.
We divided the study population based on the expression pattern of CK6. Patients with a high CK6 tumor expression had a significantly shorter survival (p = 0.013), confirmed in a multivariate cox regression model. CK6-expression is an independent marker for a decreased overall survival (HR = 1.655, 95% CI 1.158-2.365, p = 0.006). In addition, the CK6-positive tumors showed significantly less plasma cell infiltration and more cancer-associated fibroblasts (CAFs) expressing Periostin and SMA.
CK6 could be considered as an independent biomarker for a shorter overall survival. CK6 is a clinically easily accessible biomarker for the identification of the basal-like subtype of PDAC. Therefore, it could be taken into consideration in deciding for the more aggressive therapy regimes. Prospectively, studies addressing the chemosensitive characteristics of this subtype are required.
胰腺导管腺癌(PDAC)发病率的上升与治疗选择不足有关,这是一个巨大的医学挑战。需要进一步的生物标志物来识别那些将从更积极的治疗中受益的患者。
PANCALYZE 研究小组纳入了 320 名患者。进行细胞角蛋白 6(CK6)免疫组织化学染色,作为 PDAC 基底样亚型的潜在标志物。分析 CK6 表达模式与生存数据以及(炎症)肿瘤微环境的各种标志物之间的相关性。
我们根据 CK6 的表达模式将研究人群进行了分组。CK6 肿瘤高表达的患者的生存时间明显更短(p=0.013),这在多变量 Cox 回归模型中得到了证实。CK6 表达是总生存时间缩短的独立标志物(HR=1.655,95%CI 1.158-2.365,p=0.006)。此外,CK6 阳性肿瘤的浆细胞浸润明显减少,表达 Periostin 和 SMA 的癌相关成纤维细胞(CAFs)更多。
CK6 可被视为总生存时间较短的独立生物标志物。CK6 是一种临床易于获取的生物标志物,可用于识别 PDAC 的基底样亚型。因此,在决定更积极的治疗方案时,可以考虑使用 CK6。前瞻性研究需要研究该亚型的化疗敏感性特征。