Department of Gastroenterology and Medicine, Faculty of Medicine, Fukuoka University, Fukuoka, Japan
Department of Cell Biology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Anticancer Res. 2022 Aug;42(8):4103-4109. doi: 10.21873/anticanres.15908.
BACKGROUND/AIM: Recently, endoscopic ultrasound-guided fine-needle biopsy (EUS-FNB) has been conducted for diagnosing pancreatic ductal adenocarcinoma (PDAC), after which obtained samples were used in organoid cultures. However, no standardized method for PDAC organoid cultures exists. Therefore, to standardize or simplify sample collection and culture methods for PDAC organoids, we performed a floating culture using non-minced specimens obtained by EUS-FNB in a minimal medium, lacking growth factors or inhibitors for pancreatic organoids.
A total of 38 patients with clinically diagnosed PDAC were enrolled in the study. First, EUS-FNB was conducted using a 22- or 25-gauge biopsy needle. Then, a surplus of samples was collected for organoid formation after rapid on-site cytological evaluations of sample adequacy. Subsequently, the established organoids were compared with clinical data and pathological diagnosis, following periodic observations and evaluations for morphology.
PDAC organoids were successfully created in 24 of the 38 cases (63.2%), including four cases with pathologically inconclusive EUS-FNB results. Afterward, PDAC organoid morphology was classified into ductal, dormant, and adhesive small cluster (ASC) types. Although the ductal and ASC types were seen separately, they were also seen together in other cases, which we named "mixed type".
We propose a feasible and straightforward method for establishing organoids, especially for diagnosing PDAC, particularly when the result of EUS-FNB is pathologically inconclusive. Furthermore, PDAC organoids are morphologically classified into three types reported for the first time.
背景/目的:最近,内镜超声引导下细针活检(EUS-FNB)已用于诊断胰腺导管腺癌(PDAC),之后获得的样本用于类器官培养。然而,PDAC 类器官培养尚无标准化方法。因此,为了标准化或简化 PDAC 类器官的样本采集和培养方法,我们使用 EUS-FNB 获得的非切碎标本在缺乏胰腺类器官生长因子或抑制剂的最小培养基中进行漂浮培养。
共纳入 38 例临床诊断为 PDAC 的患者。首先,使用 22 或 25 号活检针进行 EUS-FNB。然后,在快速进行现场细胞学评估以确定样本充足后,收集多余的样本进行类器官形成。随后,将建立的类器官与临床数据和病理诊断进行比较,并定期观察和评估形态。
38 例中有 24 例(63.2%)成功建立了 PDAC 类器官,其中 4 例 EUS-FNB 结果病理不确定。随后,将 PDAC 类器官形态分为导管型、休眠型和粘附小簇(ASC)型。尽管导管型和 ASC 型分别可见,但在其他病例中也可见到它们一起存在,我们将其命名为“混合型”。
我们提出了一种可行且简单的建立类器官的方法,特别是在 EUS-FNB 结果病理不确定时用于诊断 PDAC。此外,首次对 PDAC 类器官进行了三种形态学分类。