Decreased CT-number in the pancreatic parenchyma is a reliable imaging biomarker of the presence of malignancies in patients with high-risk intraductal papillary mucinous neoplasm.


Journal

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]
ISSN: 1424-3911
Titre abrégé: Pancreatology
Pays: Switzerland
ID NLM: 100966936

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 27 09 2019
revised: 29 01 2020
accepted: 18 02 2020
pubmed: 9 3 2020
medline: 27 2 2021
entrez: 9 3 2020
Statut: ppublish

Résumé

Intraductal papillary mucinous neoplasm (IPMN) is a premalignant cystic neoplasm of the pancreas and is frequently detected in imaging investigations. A proportion of the patients with IPMN develop malignancies including high-grade dysplasia and invasive carcinoma. To predict the presence of malignancies in IPMN, constant imaging follow-up is usually required. Pancreatic steatosis (PS) has been recently identified as a facilitating factor for pancreatic cancer, and can be predicted through computed tomography (CT). We hypothesized that the CT-number of the pancreatic parenchyma could be a new reliable imaging biomarker for IPMN patients. Eighty-six patients undergoing pancreatectomy for IPMN were investigated. Using preoperative CT, the pancreatic index (PI) was calculated by dividing the CT-number of the pancreas by that of the spleen. Malignancies were pathologically detected in 63 cases (73.3%). Patients were divided into two cohorts according to the presence of malignancies and were compared for various factors including the PI scores. The comparison of the two cohorts detected significant differences in two parameters (CA19-9 and PI score), and the PI score was the most sensitive biomarker to predict the presence of malignancies in patients showing high-risk stigmata of IPMN. Pancreatic CT-number is an additional reliable imaging biomarker in distinguishing patients with IPMN having malignancies when investigating the patients showing high-risk stigmata.

Sections du résumé

BACKGROUND BACKGROUND
Intraductal papillary mucinous neoplasm (IPMN) is a premalignant cystic neoplasm of the pancreas and is frequently detected in imaging investigations. A proportion of the patients with IPMN develop malignancies including high-grade dysplasia and invasive carcinoma. To predict the presence of malignancies in IPMN, constant imaging follow-up is usually required. Pancreatic steatosis (PS) has been recently identified as a facilitating factor for pancreatic cancer, and can be predicted through computed tomography (CT). We hypothesized that the CT-number of the pancreatic parenchyma could be a new reliable imaging biomarker for IPMN patients.
METHODS METHODS
Eighty-six patients undergoing pancreatectomy for IPMN were investigated. Using preoperative CT, the pancreatic index (PI) was calculated by dividing the CT-number of the pancreas by that of the spleen.
RESULTS RESULTS
Malignancies were pathologically detected in 63 cases (73.3%). Patients were divided into two cohorts according to the presence of malignancies and were compared for various factors including the PI scores. The comparison of the two cohorts detected significant differences in two parameters (CA19-9 and PI score), and the PI score was the most sensitive biomarker to predict the presence of malignancies in patients showing high-risk stigmata of IPMN.
CONCLUSIONS CONCLUSIONS
Pancreatic CT-number is an additional reliable imaging biomarker in distinguishing patients with IPMN having malignancies when investigating the patients showing high-risk stigmata.

Identifiants

pubmed: 32146046
pii: S1424-3903(20)30050-8
doi: 10.1016/j.pan.2020.02.014
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

442-447

Informations de copyright

Copyright © 2020 IAP and EPC. Published by Elsevier B.V. All rights reserved.

Auteurs

Tomoki Abe (T)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Daisaku Yamada (D)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Kei Asukai (K)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Shinichiro Hasegawa (S)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Akira Tomokuni (A)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Hiroshi Wada (H)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Wataru Fujii (W)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Kenji Ikezawa (K)

Department of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Nobuyasu Fukutake (N)

Department of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Kazuyoshi Ohkawa (K)

Department of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Naoki Shinno (N)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Hisashi Hara (H)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Yoshitomo Yanagimoto (Y)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Yusuke Takahashi (Y)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Keijiro Sugimura (K)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Kazuyoshi Yamamoto (K)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Hajime Ushigome (H)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Naotsugu Haraguchi (N)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Junichi Nishimura (J)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Masayoshi Yasui (M)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Takeshi Omori (T)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Hiroshi Miyata (H)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Masayuki Ohue (M)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Masahiko Yano (M)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Masato Sakon (M)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.

Hidenori Takahashi (H)

Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan. Electronic address: takahasi-hi@mc.pref.osaka.jp.

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