Risk Factors and Incidence of Gastric Cancer After Detection of Helicobacter pylori Infection: A Large Cohort Study.


Journal

Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630

Informations de publication

Date de publication:
02 2020
Historique:
received: 31 07 2019
revised: 13 09 2019
accepted: 16 10 2019
pubmed: 28 10 2019
medline: 19 5 2020
entrez: 27 10 2019
Statut: ppublish

Résumé

Nearly all studies of gastric adenocarcinoma in the United States have relied on national cancer databases, which do not include data on Helicobacter pylori infection, the most well-known risk factor for gastric cancer. We collected data from a large cohort of patients in the United States to calculate the incidence of and risk factors for nonproximal gastric adenocarcinomas after detection of H pylori. Secondary aims included identifying how treatment and eradication affect cancer risk. We performed a retrospective cohort study, collecting data from the Veterans Health Administration on 371,813 patients (median age 62 years; 92.3% male) who received a diagnosis of H pylori infection from January 1, 1994, through December 31, 2018. The primary outcome was a diagnosis of distal gastric adenocarcinoma 30 days or more after detection of H pylori infection. We performed a time to event with competing risk analysis (with death before cancer as a competing risk). The cumulative incidence of cancer at 5, 10, and 20 years after detection of H pylori infection was 0.37%, 0.5%, and 0.65%, respectively. Factors associated with cancer included older age at time of detection of H pylori infection (subhazard ratio [SHR], 1.13; 95% confidence interval [CI], 1.11-1.15; P < .001), black/African American race (SHR, 2.00; 95% CI, 1.80-2.22), Asian race (SHR, 2.52; 95% CI, 1.64-3.89) (P < .001 for race), Hispanic or Latino ethnicity (SHR, 1.59; 95% CI, 1.34-1.87; P < .001), and history of smoking (SHR, 1.38; 95% CI, 1.25-1.52; P < .001). Women had decreased risk of gastric adenocarcinoma compared with men (SHR, 0.52; 95% CI, 0.40-0.68; P < .001); patients whose H pylori infection was detected based on serum antibody positivity also had a reduced risk of cancer (SHR 0.74; 95% CI, 0.54-1.04; P = .04). Patients who received treatment for their H pylori infection still had an increased risk of gastric cancer (SHR, 1.16; 95% CI, 0.74-1.83; P = .51) but confirmed H pylori eradication after treatment reduced risk of gastric cancer (SHR, 0.24; 95% CI, 0.15-0.41; P < .001). In a study of 371,813 veterans with a diagnosis of H pylori infection, we found significantly higher risks of gastric cancer in racial and ethnic minorities and smokers. Treatment of H pylori infection decreased risk only if eradication was successful. Studies are needed on the effects of screening high-risk persons and to identify quality measures for diagnosis, resistance patterns, and treatment efficacy.

Sections du résumé

BACKGROUND & AIMS
Nearly all studies of gastric adenocarcinoma in the United States have relied on national cancer databases, which do not include data on Helicobacter pylori infection, the most well-known risk factor for gastric cancer. We collected data from a large cohort of patients in the United States to calculate the incidence of and risk factors for nonproximal gastric adenocarcinomas after detection of H pylori. Secondary aims included identifying how treatment and eradication affect cancer risk.
METHODS
We performed a retrospective cohort study, collecting data from the Veterans Health Administration on 371,813 patients (median age 62 years; 92.3% male) who received a diagnosis of H pylori infection from January 1, 1994, through December 31, 2018. The primary outcome was a diagnosis of distal gastric adenocarcinoma 30 days or more after detection of H pylori infection. We performed a time to event with competing risk analysis (with death before cancer as a competing risk).
RESULTS
The cumulative incidence of cancer at 5, 10, and 20 years after detection of H pylori infection was 0.37%, 0.5%, and 0.65%, respectively. Factors associated with cancer included older age at time of detection of H pylori infection (subhazard ratio [SHR], 1.13; 95% confidence interval [CI], 1.11-1.15; P < .001), black/African American race (SHR, 2.00; 95% CI, 1.80-2.22), Asian race (SHR, 2.52; 95% CI, 1.64-3.89) (P < .001 for race), Hispanic or Latino ethnicity (SHR, 1.59; 95% CI, 1.34-1.87; P < .001), and history of smoking (SHR, 1.38; 95% CI, 1.25-1.52; P < .001). Women had decreased risk of gastric adenocarcinoma compared with men (SHR, 0.52; 95% CI, 0.40-0.68; P < .001); patients whose H pylori infection was detected based on serum antibody positivity also had a reduced risk of cancer (SHR 0.74; 95% CI, 0.54-1.04; P = .04). Patients who received treatment for their H pylori infection still had an increased risk of gastric cancer (SHR, 1.16; 95% CI, 0.74-1.83; P = .51) but confirmed H pylori eradication after treatment reduced risk of gastric cancer (SHR, 0.24; 95% CI, 0.15-0.41; P < .001).
CONCLUSIONS
In a study of 371,813 veterans with a diagnosis of H pylori infection, we found significantly higher risks of gastric cancer in racial and ethnic minorities and smokers. Treatment of H pylori infection decreased risk only if eradication was successful. Studies are needed on the effects of screening high-risk persons and to identify quality measures for diagnosis, resistance patterns, and treatment efficacy.

Identifiants

pubmed: 31654635
pii: S0016-5085(19)41464-9
doi: 10.1053/j.gastro.2019.10.019
pmc: PMC7010558
mid: NIHMS1542500
pii:
doi:

Substances chimiques

Antacids 0
Anti-Bacterial Agents 0
Proton Pump Inhibitors 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

527-536.e7

Subventions

Organisme : NIDDK NIH HHS
ID : T32 DK007740
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 AGA Institute. Published by Elsevier Inc. All rights reserved.

Références

Cancer Epidemiol Biomarkers Prev. 2014 May;23(5):700-13
pubmed: 24618998
Gut Liver. 2016 Mar;10(2):157-9
pubmed: 26934879
US Gastroenterol Hepatol Rev. 2011 Jun;7(1):59-64
pubmed: 21857882
Gastroenterology. 2009 Nov;137(5):1641-8.e1-2
pubmed: 19664631
CA Cancer J Clin. 2012 Sep-Oct;62(5):283-98
pubmed: 22987332
World J Gastroenterol. 2018 Jul 7;24(25):2722-2732
pubmed: 29991877
N Engl J Med. 1991 Oct 17;325(16):1132-6
pubmed: 1891021
Aliment Pharmacol Ther. 2000 May;14(5):625-34
pubmed: 10792127
Cancer Epidemiol Biomarkers Prev. 2011 May;20(5):826-34
pubmed: 21357376
EMBO Rep. 2006 May;7(5):470-3
pubmed: 16670677
Clin Gastroenterol Hepatol. 2018 Jul;16(7):992-1002.e6
pubmed: 29559361
Gastroenterology. 2018 Nov;155(5):1372-1382.e17
pubmed: 29990487
Int J Cancer. 2015 Mar 1;136(5):E359-86
pubmed: 25220842
Helicobacter. 2017 Oct;22(5):
pubmed: 28771894
Cancer. 2014 May 1;120(9):1290-314
pubmed: 24343171
Aliment Pharmacol Ther. 2008 Dec 1;28(11-12):1309-16
pubmed: 18761703
World J Gastroenterol. 2014 Sep 7;20(33):11552-9
pubmed: 25206262
Ann Surg Oncol. 2008 Jun;15(6):1644-50
pubmed: 18392661
N Engl J Med. 2019 Mar 21;380(12):1158-1165
pubmed: 30893536
Gastroenterol Hepatol Bed Bench. 2011 Fall;4(4):175-85
pubmed: 24834180
CA Cancer J Clin. 2019 Jan;69(1):7-34
pubmed: 30620402
CA Cancer J Clin. 2011 Mar-Apr;61(2):69-90
pubmed: 21296855
Clin Gastroenterol Hepatol. 2020 Feb;18(2):347-359.e5
pubmed: 31154030
Cleve Clin J Med. 2018 Dec;85(12):928-930
pubmed: 30526758
Int J Cancer. 2010 Dec 15;127(12):2893-917
pubmed: 21351269
J Gastrointest Cancer. 2015 Mar;46(1):21-8
pubmed: 25412859
Gut. 2001 Sep;49(3):347-53
pubmed: 11511555
BMJ. 2014 May 20;348:g3174
pubmed: 24846275
Gastroenterology. 2018 Jul;155(1):67-75
pubmed: 29550592
Dig Dis Sci. 2014 Dec;59(12):3027-34
pubmed: 25030941
Cancer Res. 1995 Feb 1;55(3):562-5
pubmed: 7834625
Cancer. 2017 Dec 15;123 Suppl 24:4994-5013
pubmed: 29205310
Gastrointest Endosc. 2016 Jul;84(1):18-28
pubmed: 26940296
Gut. 2013 May;62(5):676-82
pubmed: 22698649
World J Gastroenterol. 2019 Jun 21;25(23):2878-2886
pubmed: 31249446
FASEB J. 2014 Sep;28(9):3821-3822
pubmed: 29405744
Gastroenterology. 2018 Sep;155(3):648-660
pubmed: 29778607
Gastroenterology. 2019 Jan;156(1):59-62.e4
pubmed: 30267713
Aliment Pharmacol Ther. 2007 Apr 1;25(7):805-12
pubmed: 17373919
Prz Gastroenterol. 2019;14(1):26-38
pubmed: 30944675
Ann Surg Oncol. 2015 Sep;22(9):2965-71
pubmed: 25631065
Gastroenterology. 2017 Aug;153(2):420-429
pubmed: 28456631
Gastroenterology. 2019 Jul;157(1):44-53
pubmed: 30998990
Lancet Infect Dis. 2018 Mar;18(3):318-327
pubmed: 29276051
Cancer Lett. 2014 Apr 10;345(2):196-202
pubmed: 23981572
Gut. 2018 Dec;67(12):2092-2096
pubmed: 29382776
Front Biosci (Landmark Ed). 2009 Jan 01;14:1490-504
pubmed: 19273142
Gastrointest Endosc. 2012 Dec;76(6):1087-94
pubmed: 23164510
Mil Med. 2017 Jul;182(7):e1883-e1891
pubmed: 28810986
Cancer Prev Res (Phila). 2011 Sep;4(9):1426-35
pubmed: 21680705
J Gastrointestin Liver Dis. 2010 Jun;19(2):131-4
pubmed: 20593044
Clin Gastroenterol Hepatol. 2020 May;18(5):1235-1237.e1
pubmed: 31336199
Gan To Kagaku Ryoho. 2011 Mar;38(3):353-7
pubmed: 21403436
Gastroenterology. 2016 May;150(5):1113-1124.e5
pubmed: 26836587
N Engl J Med. 2011 Oct 13;365(15):1375-83
pubmed: 21995385
Clin Gastroenterol Hepatol. 2019 Feb;17(3):429-439
pubmed: 29902641
N Engl J Med. 1991 Oct 17;325(16):1127-31
pubmed: 1891020
J Clin Oncol. 2012 Oct 1;30(28):3507-15
pubmed: 22949151
Am J Surg Pathol. 1995;19 Suppl 1:S37-43
pubmed: 7762738
World J Gastroenterol. 2010 Jul 14;16(26):3226-34
pubmed: 20614477
J Am Med Inform Assoc. 2013 Jul-Aug;20(4):652-8
pubmed: 23396545

Auteurs

Shria Kumar (S)

Division of Gastroenterology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA. Electronic address: shriakumar@gmail.com.

David C Metz (DC)

Division of Gastroenterology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.

Susan Ellenberg (S)

Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.

David E Kaplan (DE)

Division of Gastroenterology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA; Division of Gastroenterology, Veterans Health Administration, Philadelphia, PA.

David S Goldberg (DS)

Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA; Division of Digestive Health and Liver Diseases, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL.

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Classifications MeSH