Zum Hauptinhalt springen

Value of upper gastrointestinal endoscopy for gastric cancer surveillance in patients with Lynch syndrome.

Ladigan-Badura, S ; Vangala, DB ; et al.
In: International journal of cancer, Jg. 148 (2021), Heft 1, S. 106-114
Online academicJournal

Titel:
Value of upper gastrointestinal endoscopy for gastric cancer surveillance in patients with Lynch syndrome.
Autor/in / Beteiligte Person: Ladigan-Badura, S ; Vangala, DB ; Engel, C ; Bucksch, K ; Hueneburg, R ; Perne, C ; Nattermann, J ; Steinke-Lange, V ; Rahner, N ; Schackert, HK ; Weitz, J ; Kloor, M ; Kuhlkamp, J ; Nguyen, HP ; Moeslein, G ; Strassburg, C ; Morak, M ; Holinski-Feder, E ; Buettner, R ; Aretz, S ; Loeffler, M ; Schmiegel, W ; Pox, C ; Schulmann, K
Link:
Zeitschrift: International journal of cancer, Jg. 148 (2021), Heft 1, S. 106-114
Veröffentlichung: 1995- : New York, NY : Wiley-Liss ; <i>Original Publication</i>: 1966-1984 : Genève : International Union Against Cancer, 2021
Medientyp: academicJournal
ISSN: 1097-0215 (electronic)
DOI: 10.1002/ijc.33294
Schlagwort:
  • Adult
  • Age Factors
  • Aged
  • Colorectal Neoplasms, Hereditary Nonpolyposis genetics
  • Early Detection of Cancer standards
  • Early Detection of Cancer statistics & numerical data
  • Evaluation Studies as Topic
  • Gastric Mucosa diagnostic imaging
  • Gastric Mucosa pathology
  • Gastroscopy standards
  • Genetic Predisposition to Disease
  • Germany epidemiology
  • Humans
  • Male
  • Middle Aged
  • MutL Protein Homolog 1 genetics
  • MutS Homolog 2 Protein genetics
  • Mutation
  • Neoplasm Staging
  • Patient Compliance statistics & numerical data
  • Practice Guidelines as Topic
  • Prospective Studies
  • Stomach Neoplasms epidemiology
  • Stomach Neoplasms genetics
  • Stomach Neoplasms pathology
  • Colorectal Neoplasms, Hereditary Nonpolyposis complications
  • Early Detection of Cancer methods
  • Gastroscopy statistics & numerical data
  • Stomach Neoplasms diagnosis
Sonstiges:
  • Nachgewiesen in: MEDLINE
  • Sprachen: English
  • Corporate Authors: German Consortium for Familial Intestinal Cancer
  • Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
  • Language: English
  • [Int J Cancer] 2021 Jan 01; Vol. 148 (1), pp. 106-114. <i>Date of Electronic Publication: </i>2020 Oct 13.
  • MeSH Terms: Colorectal Neoplasms, Hereditary Nonpolyposis / *complications ; Early Detection of Cancer / *methods ; Gastroscopy / *statistics & numerical data ; Stomach Neoplasms / *diagnosis ; Adult ; Age Factors ; Aged ; Colorectal Neoplasms, Hereditary Nonpolyposis / genetics ; Early Detection of Cancer / standards ; Early Detection of Cancer / statistics & numerical data ; Evaluation Studies as Topic ; Gastric Mucosa / diagnostic imaging ; Gastric Mucosa / pathology ; Gastroscopy / standards ; Genetic Predisposition to Disease ; Germany / epidemiology ; Humans ; Male ; Middle Aged ; MutL Protein Homolog 1 / genetics ; MutS Homolog 2 Protein / genetics ; Mutation ; Neoplasm Staging ; Patient Compliance / statistics & numerical data ; Practice Guidelines as Topic ; Prospective Studies ; Stomach Neoplasms / epidemiology ; Stomach Neoplasms / genetics ; Stomach Neoplasms / pathology
  • References: Hampel H, Stephens JA, Pukkala E, et al. Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset. Gastroenterology. 2005;129:415-421. ; Aaltonen LA, Salovaara R, Kristo P, et al. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med. 1998;338:1481-1487. ; Salovaara R, Loukola A, Kristo P, et al. Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J Clin Oncol. 2000;18:2193-2200. ; Hampel H, de la Chapelle A. How do we approach the goal of identifying everybody with Lynch syndrome? Fam Cancer. 2013;12:313-317. ; Watson P, Lynch HT. The tumor spectrum in HNPCC. Anticancer Res. 1994;14:1635-1639. ; Lamberti C, Mangold E, Pagenstecher C, et al. Frequency of hereditary non-polyposis colorectal cancer among unselected patients with colorectal cancer in Germany. Digestion. 2006;74:58-67. ; Win AK, Jenkins MA, Dowty JG, et al. Prevalence and penetrance of major genes and polygenes for colorectal cancer. Cancer Epidemiol Biomarkers Prev. 2017;26:404-412. ; Aarnio M, Sankila R, Pukkala E, et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer. 1999;81:214-218. ; Krapcho M, Miller D, Brest A, Yu M, Ruhl J, Tatalovich Z, Mariotto A, Lewis DR, Chen HS, Feuer EJ, Cronin KA (eds). SEER Cancer Statistics Review, 1975-2015, National Cancer Institute. Bethesda, MD, https://seer.cancer.gov/csr/1975_2015/, based on November 2017 SEER data submission, posted to the SEER web site, April 2018. ; Capelle LG, Van Grieken NC, Lingsma HF, et al. Risk and epidemiological time trends of gastric cancer in Lynch syndrome carriers in The Netherlands. Gastroenterology. 2010;138:487-492. ; Engel C, Loeffler M, Steinke V, et al. Risks of less common cancers in proven mutation carriers with lynch syndrome. J Clin Oncol. 2012;30:4409-4415. ; Barrow E, Robinson L, Alduaij W, et al. Cumulative lifetime incidence of extracolonic cancers in Lynch syndrome: a report of 121 families with proven mutations. Clin Genet. 2009;75:141-149. ; Bericht zum Krebsgeschehen in Deutschland 2016. Zentrum für Krebsregisterdaten im Robert Koch-Institut (Hrsg). Berlin. ; Therkildsen C, Ladelund S, Smith-Hansen L, Lindberg LJ, Nilbert M. Towards gene- and gender-based risk estimates in Lynch syndrome; age-specific incidences for 13 extra-colorectal cancer types. Br J Cancer. 2017;117:1702-1710. ; Karimi M, von Salome J, Aravidis C, et al. A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families. Hered Cancer Clin Pract. 2018;16:16. ; Schmiegel W, Buchberger B, Follmann M, et al. S3-Leitlinie - Kolorektales Karzinom. Z Gastroenterol. 2017;55:1344-1498. ; Uitgave van de. Stichting Opsporing Erfelijke Tumoren en de Vereniging Klinische Genetica Nederland, Werkgroep Klinische Oncogenetica. Erfelijke tumoren: Richtlijnen voor diagnostiek en preventie. 2017. ISBN/EAN 978-90-806183-0-5. ; NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®). Genetic/Familial High-Risk Assessment: Colorectal. Version 2.2019 https://www.nccn.org/professionals/physician_gls/pdf/genetics_colon.pdf. Accessed August 8, 2019. ; Goecke T, Schulmann K, Engel C, et al. Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC consortium. J Clin Oncol. 2006;24:4285-4292. ; Mangold E, Pagenstecher C, Friedl W, et al. Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer. Int J Cancer. 2005;116:692-702. ; Engel C, Rahner N, Schulmann K, et al. Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer. Clin Gastroenterol Hepatol. 2010;8:174-182. ; Saragoni L, Scarpi E, Ravaioli A, et al. Early gastric cancer: clinical behavior and treatment options. Results of an Italian Multicenter Study on Behalf of the Italian Gastric Cancer Research Group (GIRCG). Oncologist. 2018;23:852-858. ; Sano T, Katai H, Sasako M, Maruyama K. The management of early gastric cancer. Surg Oncol. 2000;9:17-22. ; Japanese Gastric Cancer Association. Japanese classification of gastric carcinoma: 3rd English edition. Gastric Cancer. 2011;14:101-112. ; Brierley JD, Gospodarowicz MK, Wittekind C, eds. TNM Classification of Malignant Tumors. Hoboken, NJ: Wiley-Blackwell; 2016. ; Schulmann K, Engel C, Propping P, Schmiegel W. Small bowel cancer risk in Lynch syndrome. Gut. 2008;57:1629-1630. ; Bonadona V, Bonaiti B, Olschwang S, et al. Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. JAMA. 2011;305:2304-2310. ; Dominguez-Valentin M, Sampson JR, Seppala TT, et al. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the prospective Lynch syndrome database. Genet Med. 2020;22:15-25. ; Watson P, Vasen HF, Mecklin JP, et al. The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome. Int J Cancer. 2008;123:444-449. ; Vasen HF, Stormorken A, Menko FH, et al. MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families. J Clin Oncol. 2001;19:4074-4080. ; Geary J, Sasieni P, Houlston R, et al. Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC). Fam Cancer. 2008;7:163-172. ; Kastrinos F, Stoffel EM, Balmana J, Steyerberg EW, Mercado R, Syngal S. Phenotype comparison of MLH1 and MSH2 mutation carriers in a cohort of 1,914 individuals undergoing clinical genetic testing in the United States. Cancer Epidemiol Biomarkers Prev. 2008;17:2044-2051. ; Jager AC, Bisgaard ML, Myrhoj T, Bernstein I, Rehfeld JF, Nielsen FC. Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression. Am J Hum Genet. 1997;61:129-138. ; Ten Broeke SW, van der Klift HM, Tops CMJ, et al. Cancer risks for PMS2-associated Lynch syndrome. J Clin Oncol. 2018;36:2961-2968. ; Koornstra JJ, Mourits MJ, Sijmons RH, Leliveld AM, Hollema H, Kleibeuker JH. Management of extracolonic tumours in patients with Lynch syndrome. Lancet Oncol. 2009;10:400-408. ; Lynch HT, Lynch PM, Lanspa SJ, Snyder CL, Lynch JF, Boland CR. Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications. Clin Genet. 2009;76:1-18. ; Hendriks YM, de Jong AE, Morreau H, et al. Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for clinicians. CA Cancer J Clin. 2006;56:213-225. ; Lindor NM, Petersen GM, Hadley DW, et al. Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review. JAMA. 2006;296:1507-1517. ; Gupta S, Provenzale D, Regenbogen SE, et al. NCCN guidelines insights: genetic/familial high-risk assessment: colorectal, version 3.2017. J Natl Compr Canc Netw. 2017;15:1465-1475. ; Provenzale D, Gupta S, Ahnen DJ, et al. Genetic/familial high-risk assessment: colorectal version 1.2016, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. 2016;14:1010-1030. ; Giardiello FM, Allen JI, Axilbund JE, et al. Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer. Am J Gastroenterol. 2014;109:1159-1179. ; Kim J, Braun D, Ukaegbu C, et al. Clinical factors associated with gastric cancer in individuals with Lynch syndrome. Clin Gastroenterol. Hepatol. 2020;18(4):830-837.e1. http://dx.doi.org/10.1016/j.cgh.2019.07.012. ; Renkonen-Sinisalo L, Sipponen P, Aarnio M, et al. No support for endoscopic surveillance for gastric cancer in hereditary non-polyposis colorectal cancer. Scand J Gastroenterol. 2002;37:574-577. ; Soer EC, Leicher LW, Langers AM, et al. Equivalent Helicobacter pylori infection rates in Lynch syndrome mutation carriers with and without a first-degree relative with gastric cancer. Int J Colorectal Dis. 2016;31:693-697. ; Galiatsatos P, Labos C, Jeanjean M, Miller K, Foulkes WD. Low yield of gastroscopy in patients with Lynch syndrome. Turk J Gastroenterol. 2017;28:434-438. ; Moller P, Seppala TT, Bernstein I, et al. Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the prospective Lynch syndrome database. Gut. 2017;66:1657-1664.
  • Contributed Indexing: Keywords: HNPCC; Lynch syndrome; gastric cancer; screening; surveillance
  • Substance Nomenclature: 0 (MLH1 protein, human) ; EC 3.6.1.3 (MSH2 protein, human) ; EC 3.6.1.3 (MutL Protein Homolog 1) ; EC 3.6.1.3 (MutS Homolog 2 Protein)
  • Entry Date(s): Date Created: 20200915 Date Completed: 20210610 Latest Revision: 20210610
  • Update Code: 20240513

Klicken Sie ein Format an und speichern Sie dann die Daten oder geben Sie eine Empfänger-Adresse ein und lassen Sie sich per Email zusenden.

oder
oder

Wählen Sie das für Sie passende Zitationsformat und kopieren Sie es dann in die Zwischenablage, lassen es sich per Mail zusenden oder speichern es als PDF-Datei.

oder
oder

Bitte prüfen Sie, ob die Zitation formal korrekt ist, bevor Sie sie in einer Arbeit verwenden. Benutzen Sie gegebenenfalls den "Exportieren"-Dialog, wenn Sie ein Literaturverwaltungsprogramm verwenden und die Zitat-Angaben selbst formatieren wollen.

xs 0 - 576
sm 576 - 768
md 768 - 992
lg 992 - 1200
xl 1200 - 1366
xxl 1366 -