IgG4-related sclerosing cholangitis may be a risk factor for cancer.


Journal

Journal of hepato-biliary-pancreatic sciences
ISSN: 1868-6982
Titre abrégé: J Hepatobiliary Pancreat Sci
Pays: Japan
ID NLM: 101528587

Informations de publication

Date de publication:
Jun 2021
Historique:
revised: 16 02 2021
received: 14 11 2020
accepted: 26 03 2021
pubmed: 2 5 2021
medline: 16 10 2021
entrez: 1 5 2021
Statut: ppublish

Résumé

The relationship between autoimmune pancreatitis (AIP) and malignancy has been reported. However, the potential risk for cancer in patients with immunoglobulin 4 (IgG4)-related sclerosing cholangitis (IgG4-SC) is unclear. The present study aimed to evaluate the incidence of cancer in IgG4-SC patients. We retrospectively collected clinical data for 121 patients diagnosed with IgG4-SC from 7 hospitals. We calculated the standardized incidence ratio (SIR) of cancer in IgG4-SC patients based on the national cancer rates. The SIR of the period after the diagnosis of IgG4-SC were calculated. The mean follow-up period was 6.4 years, with 121 IgG4-SC patients. During the follow-up period, 26 patients had cancer, and 29 cancers were diagnosed. The SIR of cancer after the diagnosis of IgG4-SC was 1.90 (95% confidence interval [CI] 1.67-2.21). The SIR of pancreatic and bile duct cancer was 10.30 and 8.88, respectively. The SIR of cancer in <1 year, 1-5 years, and >5 years after diagnosis of IgG4-SC were 2.58, 1.01, and 2.44, respectively. IgG4-SC patients have a high risk of cancer including pancreatic and bile duct cancer. The risk of cancer was high less <1 year and >5 years after diagnosis of IgG4-SC. Therefore, IgG4-SC patients may require careful long-term follow-up.

Sections du résumé

BACKGROUND/PURPOSE OBJECTIVE
The relationship between autoimmune pancreatitis (AIP) and malignancy has been reported. However, the potential risk for cancer in patients with immunoglobulin 4 (IgG4)-related sclerosing cholangitis (IgG4-SC) is unclear. The present study aimed to evaluate the incidence of cancer in IgG4-SC patients.
METHODS METHODS
We retrospectively collected clinical data for 121 patients diagnosed with IgG4-SC from 7 hospitals. We calculated the standardized incidence ratio (SIR) of cancer in IgG4-SC patients based on the national cancer rates. The SIR of the period after the diagnosis of IgG4-SC were calculated.
RESULTS RESULTS
The mean follow-up period was 6.4 years, with 121 IgG4-SC patients. During the follow-up period, 26 patients had cancer, and 29 cancers were diagnosed. The SIR of cancer after the diagnosis of IgG4-SC was 1.90 (95% confidence interval [CI] 1.67-2.21). The SIR of pancreatic and bile duct cancer was 10.30 and 8.88, respectively. The SIR of cancer in <1 year, 1-5 years, and >5 years after diagnosis of IgG4-SC were 2.58, 1.01, and 2.44, respectively.
CONCLUSIONS CONCLUSIONS
IgG4-SC patients have a high risk of cancer including pancreatic and bile duct cancer. The risk of cancer was high less <1 year and >5 years after diagnosis of IgG4-SC. Therefore, IgG4-SC patients may require careful long-term follow-up.

Identifiants

pubmed: 33931982
doi: 10.1002/jhbp.957
doi:

Substances chimiques

Immunoglobulin G 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

524-532

Informations de copyright

© 2021 Japanese Society of Hepato-Biliary-Pancreatic Surgery.

Références

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Auteurs

Yusuke Kurita (Y)

Department of Gastroenterology and Hepatology, Yokohama City University Hospital, Yokohama, Japan.

Yuji Fujita (Y)

Department of Hepato-Biliary-Pancreatic Medicine, NTT Medical Center Tokyo, Tokyo, Japan.

Yusuke Sekino (Y)

Department of Gastroenterology, Yokohama Rosai Hospital, Yokohama, Japan.

Seitaro Watanabe (S)

Department of Gastroenterology, Yokohama Sakae Kyosai Hospital, Yokohama, Japan.

Akito Iwasaki (A)

Department of Gastroenterology, Hiratsuka City Hospital, Hiratsuka, Japan.

Koichi Kagawa (K)

Department of Gastroenterology, Keiyu Hospital, Yokohama, Japan.

Emiko Tanida (E)

Department of Gastroenterology, Machida Municipal Hospital, Tokyo, Japan.

Shin Yagi (S)

Department of Gastroenterology and Hepatology, Yokohama City University Hospital, Yokohama, Japan.

Sho Hasegawa (S)

Department of Gastroenterology and Hepatology, Yokohama City University Hospital, Yokohama, Japan.

Takamitsu Sato (T)

Department of Gastroenterology and Hepatology, Yokohama City University Hospital, Yokohama, Japan.

Kunihiro Hosono (K)

Department of Gastroenterology and Hepatology, Yokohama City University Hospital, Yokohama, Japan.

Shingo Kato (S)

Department of Gastroenterology and Hepatology, Yokohama City University Hospital, Yokohama, Japan.

Noritoshi Kobayashi (N)

Department of Oncology, Yokohama City University Hospital, Yokohama, Japan.

Yasushi Ichikawa (Y)

Department of Oncology, Yokohama City University Hospital, Yokohama, Japan.

Itaru Endo (I)

Department of Gastroenterological Surgery, Yokohama City University Hospital, Yokohama, Japan.

Atsushi Nakajima (A)

Department of Gastroenterology and Hepatology, Yokohama City University Hospital, Yokohama, Japan.

Kensuke Kubota (K)

Department of Gastroenterology and Hepatology, Yokohama City University Hospital, Yokohama, Japan.

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