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

Author:

Yoshizawa Takahiro12,Uehara Takeshi2,Iwaya Mai2,Nakajima Tomoyuki2,Shimizu Akira1,Kubota Koji1,Notake Tsuyoshi1,Kitagawa Noriyuki1,Masuo Hitoshi1,Sakai Hiroki1,Hayashi Hikaru1,Tomida Hidenori1,Yamazaki Shiori1,Hirano Shohei1,Ota Hiroyoshi23,Soejima Yuji1

Affiliation:

1. Department of Surgery, Division of Gastroenterological, Hepato-Biliary-Pancreatic, Transplantation and Pediatric Surgery, Shinshu University School of Medicine, Matsumoto Japan

2. Department of Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan

3. Department of Biomedical Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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