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Clinical impact of ampulla of Vater cancer subtype classification based on immunohistochemical staining.
Kwon, Chae Hwa; Ahn, Ji Hyun; Seo, Hyung Il; Kim, Dong Uk; Han, Sung Yong; Kim, Suk; Lee, Nam Kyung; Hong, Seung Baek; Park, Young Mok; Noh, Byeong Gwan.
Afiliação
  • Kwon CH; Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
  • Ahn JH; Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
  • Seo HI; Department of Pathology, Pusan National University School of Medicine and Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
  • Kim DU; Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea. seohi71@pusan.ac.kr.
  • Han SY; Department of Surgery, Pusan National University School of Medicine and Biomedical Research Institute, Pusan National University Hospital, 179 Gudeok-Ro, Seo-Gu, Busan, 49241, South Korea. seohi71@pusan.ac.kr.
  • Kim S; Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
  • Lee NK; Department of Internal Medicine, Pusan National University School of Medicine and Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
  • Hong SB; Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
  • Park YM; Department of Internal Medicine, Pusan National University School of Medicine and Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
  • Noh BG; Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.
World J Surg Oncol ; 22(1): 5, 2024 Jan 03.
Article em En | MEDLINE | ID: mdl-38167037
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ampola Hepatopancreática / Adenocarcinoma / Neoplasias do Ducto Colédoco Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ampola Hepatopancreática / Adenocarcinoma / Neoplasias do Ducto Colédoco Idioma: En Ano de publicação: 2024 Tipo de documento: Article