Literature DB >> 12692062

Results of national registration of familial adenomatous polyposis.

S Bülow1.   

Abstract

BACKGROUND AND AIMS: The Danish Polyposis Register was established in 1971 with the aim of improving the poor prognosis of familial adenomatous polyposis (FAP), and in 1975 the register became national. The aim of the present study was to evaluate the prevalence of colorectal cancer and survival rate in FAP patients before and after the establishment of the Danish Polyposis Register. PATIENTS AND METHODS: The Danish Polyposis Register was established by collecting information on probands and construction of their pedigrees. Family members at risk were offered prophylactic endoscopic and molecular genetic examination, and affected individuals were treated by colectomy.
RESULTS: At the end of 2001, the Danish Polyposis Register included 434 patients from 165 families. The incidence rate was 1.90x10(-6) and the prevalence rate 4.65x10(-5). Colorectal cancer on the basis of FAP constituted 0.07% of all colorectal cancers in the 1990s. Colorectal cancer was diagnosed in 170/252 probands (67%) and in 5/182 call-up patients (3%) (p<0.001). The cumulative crude survival was 94% in call-up patients compared with 44% in probands (p<0.0001). A comparison of two periods, 1900-1975 and 1976-2001, demonstrated a decreased prevalence of colorectal cancer from 60% to 27% (p<0.0001), and an increased use of colectomy from 52% to 93% (p<0.00001). The cumulative crude survival in FAP showed substantial improvement with time (p<0.00001).
CONCLUSION: Since the establishment of the Danish Polyposis Register, the prevalence of colorectal cancer has decreased considerably and the prognosis has improved substantially. The work of the Danish Polyposis Register is probably the main cause of this improvement.

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Year:  2003        PMID: 12692062      PMCID: PMC1773626          DOI: 10.1136/gut.52.5.742

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  31 in total

1.  Epidemiology of familial adenomatous polyposis in Sweden: changes over time and differences in phenotype between males and females.

Authors:  J Björk; H Akerbrant; L Iselius; T Alm; R Hultcrantz
Journal:  Scand J Gastroenterol       Date:  1999-12       Impact factor: 2.423

2.  Surgical treatment of hereditary adenomatosis of the colon and rectum in Sweden during the last 20 years. Part I. Introduction. Surgical procedures used. Pre-and postoperative measures. Arrangement of follow-up. Propositi group, primary and late results.

Authors:  T Alm
Journal:  Acta Chir Scand       Date:  1975

3.  Activities of the Leeds Castle Polyposis Group.

Authors:  J M Northover
Journal:  Semin Surg Oncol       Date:  1987

4.  Upper gastrointestinal endoscopy in polyposis syndromes: familial polyposis coli and Gardner's syndrome.

Authors:  M V Sivak; D G Jagelman
Journal:  Gastrointest Endosc       Date:  1984-04       Impact factor: 9.427

5.  Causes of death in familial adenomatous polyposis.

Authors:  T S Galle; K Juel; S Bülow
Journal:  Scand J Gastroenterol       Date:  1999-08       Impact factor: 2.423

6.  Impact of screening examinations on survival in familial adenomatous polyposis.

Authors:  I Heiskanen; T Luostarinen; H J Järvinen
Journal:  Scand J Gastroenterol       Date:  2000-12       Impact factor: 2.423

7.  Surgery based on misdiagnosis of adenomatous polyposis. The Canadian Polyposis Registry experience.

Authors:  T Berk; Z Cohen; R S McLeod; J B Cullen
Journal:  Dis Colon Rectum       Date:  1987-08       Impact factor: 4.585

8.  Gastroduodenal polyps in familial polyposis coli.

Authors:  S Bülow; K B Lauritsen; A Johansen; L B Svendsen; J O Søndergaard
Journal:  Dis Colon Rectum       Date:  1985-02       Impact factor: 4.585

9.  The Danish Polyposis Register. Description of the methods of detection and evaluation of completeness.

Authors:  S Bülow
Journal:  Dis Colon Rectum       Date:  1984-06       Impact factor: 4.585

10.  The incidence and prevalence of familial polyposis coli in Denmark.

Authors:  S Bülow; N V Holm; M Hauge
Journal:  Scand J Soc Med       Date:  1986
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  58 in total

1.  FAP, gastric cancer, and genetic counseling featuring children and young adults: a family study and review.

Authors:  Henry T Lynch; Carrie Snyder; Janine M Davies; Stephen Lanspa; Jane Lynch; Zoran Gatalica; Victoria Graeve; Jason Foster
Journal:  Fam Cancer       Date:  2010-12       Impact factor: 2.375

2.  Controversies in the surgery of patients with familial adenomatous polyposis and Lynch syndrome.

Authors:  James M Church
Journal:  Fam Cancer       Date:  2016-07       Impact factor: 2.375

3.  The changing face of familial colorectal cancer.

Authors:  Ayan Banerjea; Sue Clark; Sina Dorudi
Journal:  BMJ       Date:  2005-01-01

Review 4.  [Preventive surgery for familial adenomatous polyposis coli].

Authors:  M Kadmon
Journal:  Chirurg       Date:  2005-12       Impact factor: 0.955

Review 5.  ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.

Authors:  Sapna Syngal; Randall E Brand; James M Church; Francis M Giardiello; Heather L Hampel; Randall W Burt
Journal:  Am J Gastroenterol       Date:  2015-02-03       Impact factor: 10.864

Review 6.  The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes.

Authors:  Stefan Aretz
Journal:  Dtsch Arztebl Int       Date:  2010-03-12       Impact factor: 5.594

7.  A web-based assessment of pediatrics resident medical knowledge in childhood hereditary gastrointestinal cancer predisposing syndromes.

Authors:  Julie Stoner; Yongyue Qi; Steven H Erdman; Thomas M Attard
Journal:  J Cancer Educ       Date:  2009       Impact factor: 2.037

8.  Evaluating causes of death in familial adenomatous polyposis.

Authors:  Fábio Guilherme C M de Campos; Rodrigo Oliva Perez; Antônio Rocco Imperiale; Víctor Edmond Seid; Sérgio Carlos Nahas; Ivan Cecconello
Journal:  J Gastrointest Surg       Date:  2010-07-30       Impact factor: 3.452

9.  Desmoid tumors: clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis.

Authors:  Fábio Guilherme Campos; Carlos Augusto Real Martinez; Marleny Novaes; Sérgio Carlos Nahas; Ivan Cecconello
Journal:  Fam Cancer       Date:  2015-06       Impact factor: 2.375

10.  MUTYH Associated Polyposis (MAP).

Authors:  M L M Poulsen; M L Bisgaard
Journal:  Curr Genomics       Date:  2008-09       Impact factor: 2.236

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