Tumour Budding as an Independent Prognostic Factor for Survival in Patients With Distal Bile Duct Cancer.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 20 05 2022
revised: 03 06 2022
accepted: 08 06 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 30 7 2022
Statut: ppublish

Résumé

Surgical resection is the standard treatment for bile duct cancer. However, even when surgical resection is possible, the 5-year survival rate is reportedly 25.0-55.0%. Therefore, bile duct cancer is associated with poor prognoses. We conducted a clinicopathological investigation, focusing on the histological phenomenon of tumour budding, which has previously been reported to be correlated with the survival of patients with a variety of cancers. To investigate the significance of tumour budding in distal bile duct cancer, we recruited 65 patients who underwent pancreatoduodenectomy at our institution between 1995 and 2011. Tumour budding was observed and evaluated using the 'hot spot method'. The 'low' budding group comprised 0-4 cell clusters and the 'high' budding group ≥5 cell clusters. Additionally, immunostaining was performed in high-budding areas. Tumour budding and stage were confirmed using a Cox proportional hazards model as independent prognostic factors for overall survival (p<0.05) in all patients. There was a significant association between budding and zinc finger E-box binding homeobox 1 expression, an endothelial-mesenchymal transition-induced transcription factor. In stage II cases, the prognosis was significantly worse in the 'high' budding group compared to that in the 'low' budding group. The budding phenomenon is an independent prognostic factor for patients with distal bile duct cancer. Understanding the mechanisms underlying tumour budding in distal bile duct cancer and its relationship with poor prognoses may be useful for the development of novel treatments for this disease.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Surgical resection is the standard treatment for bile duct cancer. However, even when surgical resection is possible, the 5-year survival rate is reportedly 25.0-55.0%. Therefore, bile duct cancer is associated with poor prognoses. We conducted a clinicopathological investigation, focusing on the histological phenomenon of tumour budding, which has previously been reported to be correlated with the survival of patients with a variety of cancers.
PATIENTS AND METHODS METHODS
To investigate the significance of tumour budding in distal bile duct cancer, we recruited 65 patients who underwent pancreatoduodenectomy at our institution between 1995 and 2011. Tumour budding was observed and evaluated using the 'hot spot method'. The 'low' budding group comprised 0-4 cell clusters and the 'high' budding group ≥5 cell clusters. Additionally, immunostaining was performed in high-budding areas.
RESULTS RESULTS
Tumour budding and stage were confirmed using a Cox proportional hazards model as independent prognostic factors for overall survival (p<0.05) in all patients. There was a significant association between budding and zinc finger E-box binding homeobox 1 expression, an endothelial-mesenchymal transition-induced transcription factor. In stage II cases, the prognosis was significantly worse in the 'high' budding group compared to that in the 'low' budding group.
CONCLUSION CONCLUSIONS
The budding phenomenon is an independent prognostic factor for patients with distal bile duct cancer. Understanding the mechanisms underlying tumour budding in distal bile duct cancer and its relationship with poor prognoses may be useful for the development of novel treatments for this disease.

Identifiants

pubmed: 35896221
pii: 42/8/4079
doi: 10.21873/anticanres.15905
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4079-4087

Informations de copyright

Copyright © 2022 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Goichi Nakayama (G)

Department of Surgery, Kurume University School of Medicine, Kurume, Japan.

Toru Hisaka (T)

Department of Surgery, Kurume University School of Medicine, Kurume, Japan; thisaka@med.kurume-u.ac.jp.

Hisamune Sakai (H)

Department of Surgery, Kurume University School of Medicine, Kurume, Japan.

Masanori Akashi (M)

Department of Surgery, Kurume University School of Medicine, Kurume, Japan.

Goto Yuichi (G)

Department of Surgery, Kurume University School of Medicine, Kurume, Japan.

Toshihiro Sato (T)

Department of Surgery, Kurume University School of Medicine, Kurume, Japan.

Yoshiki Naito (Y)

Department of Diagnostic Pathology, Kurume University Hospital, Kurume, Japan.

Jun Akiba (J)

Department of Diagnostic Pathology, Kurume University Hospital, Kurume, Japan.

Hirohisa Yano (H)

Department of Pathology, Kurume University School of Medicine, Kurume, Japan.

Yoshito Akagi (Y)

Department of Surgery, Kurume University School of Medicine, Kurume, Japan.

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Classifications MeSH