TY - JOUR
T1 - Multicenter study of early pancreatic cancer in Japan
AU - for the Japan Study Group on the Early Detection of Pancreatic Cancer (JEDPAC)
AU - Kanno, Atsushi
AU - Masamune, Atsushi
AU - Hanada, Keiji
AU - Maguchi, Hiroyuki
AU - Shimizu, Yasuhiro
AU - Ueki, Toshiharu
AU - Hasebe, Osamu
AU - Ohtsuka, Takao
AU - Nakamura, Masafumi
AU - Takenaka, Mamoru
AU - Kitano, Masayuki
AU - Kikuyama, Masataka
AU - Gabata, Toshifumi
AU - Yoshida, Koji
AU - Sasaki, Tamito
AU - Serikawa, Masahiro
AU - Furukawa, Toru
AU - Yanagisawa, Akio
AU - Shimosegawa, Tooru
N1 - Publisher Copyright:
© 2017 IAP and EPC
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2018/1
Y1 - 2018/1
N2 - Background/Objectives: The diagnosis of early-stage pancreatic ductal adenocarcinoma (PDAC) is still challenging. We conducted a multicenter study to clarify the clinical features of early-stage PDAC in Japan. Methods: We collected patients with stage 0 and stage I PDAC according to the sixth edition of the Japanese Classification of Pancreatic Carcinoma. We retrospectively analyzed the clinical profiles including opportunities for medical examination, imaging modalities and findings, methods of cytological diagnosis, and prognosis according to the stages at diagnosis. Results: Two hundred cases with Stage 0 and stage I PDAC were reported from 14 institutions, which accounted for approximately 0.7% and 3% of all PDAC cases, respectively. Overall, 20% of the early-stage PDAC cases were symptomatic. Indirect imaging findings such as dilatation of the main pancreatic duct were useful to detect early-stage PDAC. In particular, local fatty changes may be specific to early-stage PDAC. For preoperative pathologic diagnosis, cytology during endoscopic retrograde cholangiopancreatography was more commonly applied than endoscopic ultrasound fine-needle aspiration. Although the overall prognosis was favorable, new PDAC lesions developed in the remnant pancreas in 11.5% cases. Conclusions: This multicenter study revealed several key points concerning the diagnosis and management of early-stage PDAC, including screening of asymptomatic cases, importance of indirect imaging findings, application of cytology during endoscopic retrograde cholangiopancreatography, and the risk of carcinogenesis in the remnant pancreas.
AB - Background/Objectives: The diagnosis of early-stage pancreatic ductal adenocarcinoma (PDAC) is still challenging. We conducted a multicenter study to clarify the clinical features of early-stage PDAC in Japan. Methods: We collected patients with stage 0 and stage I PDAC according to the sixth edition of the Japanese Classification of Pancreatic Carcinoma. We retrospectively analyzed the clinical profiles including opportunities for medical examination, imaging modalities and findings, methods of cytological diagnosis, and prognosis according to the stages at diagnosis. Results: Two hundred cases with Stage 0 and stage I PDAC were reported from 14 institutions, which accounted for approximately 0.7% and 3% of all PDAC cases, respectively. Overall, 20% of the early-stage PDAC cases were symptomatic. Indirect imaging findings such as dilatation of the main pancreatic duct were useful to detect early-stage PDAC. In particular, local fatty changes may be specific to early-stage PDAC. For preoperative pathologic diagnosis, cytology during endoscopic retrograde cholangiopancreatography was more commonly applied than endoscopic ultrasound fine-needle aspiration. Although the overall prognosis was favorable, new PDAC lesions developed in the remnant pancreas in 11.5% cases. Conclusions: This multicenter study revealed several key points concerning the diagnosis and management of early-stage PDAC, including screening of asymptomatic cases, importance of indirect imaging findings, application of cytology during endoscopic retrograde cholangiopancreatography, and the risk of carcinogenesis in the remnant pancreas.
UR - http://www.scopus.com/inward/record.url?scp=85034989882&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85034989882&partnerID=8YFLogxK
U2 - 10.1016/j.pan.2017.11.007
DO - 10.1016/j.pan.2017.11.007
M3 - Article
C2 - 29170051
AN - SCOPUS:85034989882
SN - 1424-3903
VL - 18
SP - 61
EP - 67
JO - Pancreatology
JF - Pancreatology
IS - 1
ER -