Five years of prospective screening of high-risk individuals from families with familial pancreatic cancer

被引:171
作者
Langer, P. [1 ]
Kann, P. H. [2 ]
Fendrich, V. [1 ]
Habbe, N. [1 ]
Schneider, M. [1 ]
Sina, M. [3 ]
Slater, E. P. [1 ]
Heverhagen, J. T. [4 ]
Gress, T. M. [5 ]
Rothmund, M. [1 ]
Bartsch, D. K. [1 ]
机构
[1] Univ Marburg, Dept Gen Surg, D-35032 Marburg, Germany
[2] Univ Marburg, Div Endocrinol & Diabetol, D-35032 Marburg, Germany
[3] Univ Marburg, Inst Human Genet, D-35032 Marburg, Germany
[4] Univ Marburg, Dept Radiol, D-35032 Marburg, Germany
[5] Univ Marburg, Dept Gastroenterol, D-35032 Marburg, Germany
关键词
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY; PAPILLARY MUCINOUS NEOPLASMS; ULTRASOUND; DIAGNOSIS; ULTRASONOGRAPHY; ADENOCARCINOMA; SURVEILLANCE; KINDREDS; AGE;
D O I
10.1136/gut.2008.171611
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Objective: Familial pancreatic cancer (FPC) accounts for approximately 3% of all pancreatic cancer (PC) cases. It has been suggested that high-risk individuals (HRIs) should be offered a screening programme. Aim: To evaluate the diagnostic yield of a prospective screening programme in HRIs from families with FPC over a period of 5 years. Methods: HRIs of families with FPC of the National German Familial Pancreatic Cancer Registry (FaPaCa) were counselled and enrolled in a prospective, board-approved PC screening programme. Screening included clinical examination, laboratory tests, endoscopic ultrasound (EUS) and MRI with magnetic resonance cholangiopancreaticography (MRCP) and MR angiography. Results: Between June 2002 and December 2007, 76 HRIs of families with FPC took part in the screening programme with a total of 182 examination visits. Twenty-eight patients revealed abnormalities in EUS (n = 25) and/or MR/MRCP (n = 12). In 7 patients fine needle aspiration cytology was performed. Operative pancreatic explorations were performed in 7 individuals, resulting in limited resections in 6 cases. Histopathological examination of the resected specimens showed serous oligocystic adenomas (n = 3), pancreatic intraepithelial neoplasia 1 (PanIN1) lesions with lobular fibrosis (n = 1), PanIN2 lesions (n = 1) and PanIN1 lesion plus a gastric type intraductal papillary mucinous neoplasm (IPMN) (n = 1). Conclusions: In FPC an EUS/MR/MRCP-based screening programme leads to the detection of potential precursor lesions of PC. However, the yield of an extensive screening programme is low, especially since the tumourigenic value of low grade PanIN lesions is not yet defined. Taking into account the enormous psychological stress for the tested individual and the high costs, a general PC screening in HRIs is not justified.
引用
收藏
页码:1410 / 1418
页数:9
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