ABO Blood Group and Risk of Pancreatic Carcinogenesis in Intraductal Papillary Mucinous Neoplasms

被引:8
作者
Hamada, Tsuyoshi [1 ,2 ]
Oyama, Hiroki [1 ]
Nakai, Yousuke [1 ,3 ]
Tada, Minoru [1 ]
Koh, Hideo [4 ]
Tateishi, Keisuke [1 ]
Arita, Junichi [5 ]
Hakuta, Ryunosuke [1 ,3 ]
Ijichi, Hideaki [1 ]
Ishigaki, Kazunaga [1 ]
Kawaguchi, Yoshikuni [5 ]
Kogure, Hirofumi [1 ]
Mizuno, Suguru [1 ]
Morikawa, Teppei [6 ]
Saito, Kei [1 ]
Saito, Tomotaka [1 ]
Sato, Tatsuya [1 ]
Takagi, Kaoru [1 ,7 ]
Takahara, Naminatsu [1 ]
Takahashi, Ryota [1 ]
Tanaka, Atsushi [6 ]
Tanaka, Mariko [6 ]
Ushiku, Tetsuo [6 ]
Hasegawa, Kiyoshi [5 ]
Koike, Kazuhiko [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Gastroenterol, Tokyo, Japan
[2] Japanese Fdn Canc Res, Dept Hepatobiliary Pancreat Med, Canc Inst Hosp, Tokyo, Japan
[3] Univ Tokyo Hosp, Dept Endoscopy & Endoscop Surg, Tokyo, Japan
[4] Osaka City Univ, Grad Sch Med, Dept Hematol, Osaka, Japan
[5] Univ Tokyo, Grad Sch Med, Dept Surg, Hepatopancreaticobiliary Surg Div, Tokyo, Japan
[6] Univ Tokyo, Grad Sch Med, Dept Pathol, Tokyo, Japan
[7] Mitsui Mem Hosp, Dept Gastroenterol, Tokyo, Japan
基金
日本学术振兴会;
关键词
INTERNATIONAL CONSENSUS GUIDELINES; DISEASE-SPECIFIC MORTALITY; GENOME-WIDE ASSOCIATION; GROUP ALLELES; CANCER; MANAGEMENT; SUBDISTRIBUTION; SUSCEPTIBILITY; ANTIGENS; IPMNS;
D O I
10.1158/1055-9965.EPI-20-1581
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: ABO blood group has been associated with risks of various malignancies, including pancreatic cancer. No study has evaluated the association of ABO blood group with incidence of pancreatic carcinogenesis during follow-up of patients with intraductal papillary mucinous neoplasms (IPMN). Methods: Among 3,164 patients diagnosed with pancreatic cysts at the University of Tokyo (Tokyo, Japan) from 1994 through 2019, we identified 1,815 patients with IPMN with available data on ABO blood group. We studied the association of ABO blood group with incidence of pancreatic carcinoma, overall and by carcinoma types [IPMN-derived carcinoma or concomitant pancreatic ductal adenocarcinoma (PDAC)]. Utilizing competing-risks proportional hazards models, we estimated subdistribution hazard ratios (SHR) for incidence of pancreatic carcinoma with adjustment for potential confounders, including cyst characteristics. Results: During 11,518 person-years of follow-up, we identified 97 patients diagnosed with pancreatic carcinoma (53 with IPMN-derived carcinoma and 44 with concomitant PDAC). Compared with patients with blood group O, patients with blood groups A, B, and AB had multivariable SHRs (95% confidence intervals) for pancreatic carcinoma of 2.25 (1.25-4.07; P = 0.007), 2.09 (1.08-4.05; P = 0.028), and 1.17 (0.43-3.19; P = 0.76), respectively. We observed no differential association of ABO blood group with pancreatic carcinoma incidence by carcinoma types. Conclusions: In this large long-term study, patients with IPMN with blood group A or B appeared to be at higher risk of pancreatic carcinoma compared with those with blood group O. Impact: ABO blood group can be a biomarker for pancreatic cancer risk among patients with IPMNs.
引用
收藏
页码:1020 / 1028
页数:9
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