Clinical impact of ampulla of Vater cancer subtype classification based on immunohistochemical staining

World J Surg Oncol. 2024 Jan 3;22(1):5. doi: 10.1186/s12957-023-03289-y.

Abstract

Background: The histological subtype is an important prognostic factor for ampulla of Vater (AoV) cancer. This study proposes a classification system for the histological subtyping of AoV cancer based on immunohistochemical (IHC) staining and its prognostic significance.

Methods: Seventy-five AoV cancers were analyzed for cytokeratin 7 (CK7), CK20, and causal-type homeobox transcription factor 2 (CDX2) expression by IHC staining. We differentiated the subtypes (INT, intestinal; PB, pancreatobiliary; MIX, mixed; NOS, not otherwise specified) into classification I: CK7/CK20, classification II: CK7/CK20 or CDX2, classification III: CK7/CDX2 and examined their associations with clinicopathological factors.

Results: Classifications I, II, and III subtypes were INT (7, 10, and 10 cases), PB (43, 37, and 38 cases), MIX (13, 19, and 18 cases), and NOS (12, 9, and 9 cases). Significant differences in disease-free survival among the subtypes were observed in classifications II and III using CDX2; the PB and NOS subtype exhibited shorter survival time compared with INT subtype. In classification III, an association was revealed between advanced T/N stage, poor differentiation, lymphovascular invasion (LVI), the PB and NOS subtypes, and recurrence risk. In classification III, the subtypes differed significantly in T/N stage and LVI. Patients with the PB subtype had advanced T and N stages and a higher incidence of LVI.

Conclusions: Classification using CDX2 revealed subtypes with distinct prognostic significance. Combining CK7 and CDX2 or adding CDX2 to CK7/CK20 is useful for distinguishing subtypes, predicting disease outcomes, and impacting the clinical management of patients with AoV cancer.

Keywords: CDX2; CK7; Disease-free survival; Histological subtypes; Immunohistochemical staining; ampullar of Vater cancer.

MeSH terms

  • Adenocarcinoma* / pathology
  • Ampulla of Vater* / pathology
  • Biomarkers, Tumor / metabolism
  • CDX2 Transcription Factor / metabolism
  • Common Bile Duct Neoplasms* / pathology
  • Humans
  • Immunohistochemistry
  • Keratin-20 / metabolism
  • Keratin-7 / metabolism
  • Prognosis

Substances

  • Biomarkers, Tumor
  • CDX2 Transcription Factor
  • Keratin-20
  • Keratin-7