Clinical risk factors of colorectal cancer in patients with serrated polyposis syndrome: a multicentre cohort analysis

被引:81
作者
IJspeert, J. E. G. [1 ]
Rana, S. A. Q. [2 ]
Atkinson, N. S. S. [3 ]
van Herwaarden, Y. J. [4 ]
Bastiaansen, B. A. J. [1 ]
van Leerdam, M. E. [5 ]
Sanduleanu, S. [6 ]
Bisseling, T. M. [4 ]
Spaander, M. C. W. [7 ]
Clark, S. K. [2 ]
Meijer, G. A. [8 ]
van Lelyveld, N. [9 ]
Koornstra, J. J. [10 ]
Nagtegaal, I. D. [11 ]
East, J. E. [3 ]
Latchford, A. [2 ]
Dekker, E. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Gastroenterol & Hepatol, Amsterdam, Netherlands
[2] St Marks Hosp, Polyposis Registry, London, England
[3] Univ Oxford, John Radcliffe Hosp, Div Expt Med, Translat Gastroenterol Unit,Nuffield Dept Clin Me, Oxford, England
[4] Radboud Univ Nijmegen, Med Ctr, Dept Gastroenterol & Hepatol, Nijmegen, Netherlands
[5] Netherlands Canc Inst, Dept Gastroenterol & Hepatol, Amsterdam, Netherlands
[6] Maastricht Univ, GROW Sch Oncol & Dev Biol, Div Gastroenterol & Hepatol, Med Ctr, Maastricht, Netherlands
[7] Erasmus Univ, Dept Gastroenterol & Hepatol, Med Ctr, Rotterdam, Netherlands
[8] Netherlands Canc Inst, Dept Pathol, Amsterdam, Netherlands
[9] St Antonius Hosp, Dept Gastroenterol & Hepatol, Nieuwegein, Netherlands
[10] Univ Groningen, Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, Groningen, Netherlands
[11] Radboud Univ Nijmegen, Med Ctr, Dept Pathol, Nijmegen, Netherlands
关键词
ISLAND METHYLATOR PHENOTYPE; HYPERPLASTIC POLYPOSIS; PATHWAY; COLON; CLASSIFICATION; POLYPECTOMY; ADENOMAS; GENETICS; SERIES;
D O I
10.1136/gutjnl-2015-310630
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Serrated polyposis syndrome (SPS) is accompanied by an increased risk of colorectal cancer (CRC). Patients fulfilling the clinical criteria, as defined by the WHO, have a wide variation in CRC risk. We aimed to assess risk factors for CRC in a large cohort of patients with SPS and to evaluate the risk of CRC during surveillance. Design In this retrospective cohort analysis, all patients with SPS from seven centres in the Netherlands and two in the UK were enrolled. WHO criteria were used to diagnose SPS. Patients who only fulfilled WHO criterion-2, with IBD and/or a known hereditary CRC syndrome were excluded. Results In total, 434 patients with SPS were included for analysis; 127 (29.3%) were diagnosed with CRC. In a per-patient analysis >= 1 serrated polyp (SP) with dysplasia (OR 2.07; 95% CI 1.28 to 3.33), >= 1 advanced adenoma (OR 2.30; 95% CI 1.47 to 3.67) and the fulfilment of both WHO criteria 1 and 3 (OR 1.60; 95% CI 1.04 to 2.51) were associated with CRC, while a history of smoking was inversely associated with CRC (OR 0.36; 95% CI 0.23 to 0.56). Overall, 260 patients underwent surveillance after clearing of all relevant lesions, during which two patients were diagnosed with CRC, corresponding to 1.9 events/1000 person-years surveillance (95% CI 0.3 to 6.4). Conclusion The presence of SPs containing dysplasia, advanced adenomas and/or combined WHO criteria 1 and 3 phenotype is associated with CRC in patients with SPS. Patients with a history of smoking show a lower risk of CRC, possibly due to a different pathogenesis of disease. The risk of developing CRC during surveillance is lower than previously reported in literature, which may reflect a more mature multicentre cohort with less selection bias.
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收藏
页码:278 / 284
页数:7
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