An Immunohistochemical Analysis of Osteopontin and S100 Calcium-binding Protein P is Useful for Subclassifying Large- and Small-duct Type Intrahepatic Cholangiocarcinomas.

Takahiro Yoshizawa, Takeshi Uehara, Mai Iwaya, Tomoyuki Nakajima, Akira Shimizu, Koji Kubota, Tsuyoshi Notake, Noriyuki Kitagawa, Hitoshi Masuo, Hiroki Sakai, Hikaru Hayashi, Hidenori Tomida, Shiori Yamazaki, Shohei Hirano, Hiroyoshi Ota, Yuji Soejima
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Abstract

Intrahepatic cholangiocarcinoma (iCCA) has been newly subclassified into two different subtypes: large-duct (LD) type and small-duct (SD) type. However, many cases are difficult to subclassify, and there is no consensus regarding subclassification criteria. LD type expresses the highly sensitive diagnostic marker S100 calcium-binding protein P (S100P), while SD type lacks sensitive markers. We identified osteopontin (OPN) as a highly sensitive marker for SD type. This study aimed to develop new subclassification criteria for LD-type and SD-type iCCA. We retrospectively investigated 74 patients with iCCA and subclassified them based on whole-section immunostaining of S100P and OPN. Of the 74 cases, 41 were subclassified as LD type, 32 as SD type, and one was indeterminate. Notably, all S100P-negative cases had OPN positivity. Seventy-three of the 74 cases (98.6%) were clearly and easily subclassified as LD or SD type using only these 2 markers. We also determined the value of immunohistochemistry in cases that were difficult to diagnose based on hematoxylin-eosin and Alcian blue-periodic acid-Schiff staining. Furthermore, we analyzed the clinicopathological characteristics and prognoses of these 2 subtypes. LD type was a poor prognostic factor on univariate analysis; it had significantly worse overall survival (P= 0.007) and recurrence-free survival (P < 0.001) than the SD type. In conclusion, we propose new subclassification criteria for iCCA based on immunostaining of S100P and OPN. These criteria may help pathologists to diagnose subtypes of iCCA, supporting future clinical trials and the development of medications for these 2 subtypes as distinct cancers.
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骨化蛋白和 S100 钙结合蛋白 P 的免疫组化分析有助于对大导管型和小导管型肝内胆管癌进行亚分类。
肝内胆管癌(iCCA)新近被细分为两种不同的亚型:大导管型(LD)和小导管型(SD)。然而,许多病例很难进行亚分类,亚分类标准也未达成共识。LD 型表达高度敏感的诊断标志物 S100 钙结合蛋白 P(S100P),而 SD 型缺乏敏感的标志物。我们发现骨生成素(OPN)是 SD 型的高灵敏度标记物。本研究旨在为 LD 型和 SD 型 iCCA 制定新的亚分类标准。我们回顾性研究了74例iCCA患者,并根据S100P和OPN的全切片免疫染色对他们进行了亚分类。在这 74 例患者中,41 例被亚分类为 LD 型,32 例为 SD 型,1 例为不确定型。值得注意的是,所有 S100P 阴性的病例都有 OPN 阳性。74 例病例中有 73 例(98.6%)仅凭这两种标记物就能明确、轻松地分类为 LD 或 SD 型。我们还确定了免疫组化在根据苏木精-伊红和阿尔新蓝-周期酸-希夫染色难以诊断的病例中的价值。此外,我们还分析了这两种亚型的临床病理特征和预后。在单变量分析中,LD 型是一个不良预后因素;其总生存期(P= 0.007)和无复发生存期(P < 0.001)均显著低于 SD 型。总之,我们根据 S100P 和 OPN 的免疫染色提出了新的 iCCA 亚分类标准。这些标准可能有助于病理学家诊断 iCCA 的亚型,支持未来的临床试验和针对这两种亚型不同癌症的药物开发。
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