Missed Adenomas during Colonoscopic Surveillance in Individuals with Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer)

被引:91
|
作者
Stoffel, Elena M. [1 ]
Turgeon, D. Kim [2 ]
Stockwell, David H.
Zhao, Lili [3 ]
Normolle, Daniel P. [4 ]
Tuck, Missy K. [2 ]
Bresalier, Robert S. [5 ]
Marcon, Norman E. [6 ]
Baron, John A. [7 ]
Ruffin, Mack T. [2 ]
Brenner, Dean E. [2 ]
Syngal, Sapna
机构
[1] Brigham & Womens Hosp, Div Gastroenterol, Dana Farber Harvard Canc Inst, Boston, MA 02115 USA
[2] Univ Michigan, Med Ctr, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Ctr Comprehens Canc, Biostat Unit, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[5] Univ Texas Houston, MD Anderson Canc Ctr, Houston, TX 77030 USA
[6] Wellesley Site St Michaels Hosp, Toronto, ON, Canada
[7] Dartmouth Med Sch, Lebanon, NH USA
关键词
D O I
10.1158/1940-6207.CAPR-08-0098
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Aims: Lynch syndrome (also known as hereditary nonpolyposis colon cancer) is associated with an increased risk for colorectal cancer, which can arise despite frequent colonoscopic exams. We evaluated the adenoma miss rate of conventional colonoscopy in patients with Lynch syndrome, and compared the sensitivity of chromoendoscopy versus intensive inspection for detecting polyps missed by conventional colonoscopy. Methods: Fifty-four subjects with Lynch syndrome underwent tandem colonoscopies at four centers of the Great Lakes- New England Clinical Epidemiology and Validation Center of the Early Detection Research Network. All participants first had a conventional colonoscopy with removal of all visualized polyps. The second endoscopy was randomly assigned as either pancolonic indigo carmine chromoendoscopy or standard colonoscopy with intensive inspection lasting >20 minutes. Size, histology, and number of polyps detected on each exam were recorded. Results: After undergoing standard colonoscopy, 28 individuals were randomized to a second exam with chromoendoscopy and 26 underwent intensive inspection. The mean interval since last colonoscopy was 17.5 months. Seventeen polyps (10 adenomas and 7 hyperplastic polyps) were identified on the first standard colonoscopies. Twenty-three additional polyps (12 adenomas and 11 hyperplastic polyps) were found on the second exams, yielding an adenoma miss rate of 55%. Fifteen polyps (5 adenomas and 10 hyperplastic polyps) were found in subjects who had chromoendoscopy and 8 polyps (7 adenomas and 1 hyperplastic polyp) in those who had intensive inspection. Chromoendoscopy was associated with more normal tissue biopsies (11 versus 5) and longer procedure times compared with intensive inspection (29.8 +/- 9.5 versus 25.3 +/- 5.8 minutes; P = 0.04). Controlling for age, number of previous colonoscopies, procedure time, and prior colonic resection, chromoendoscopy detected more polyps (P = 0.04), but adenoma detection was not significantly different compared with intensive inspection (P = 0.27). Conclusions: Small adenomas are frequently missed in patients with Lynch syndrome. Although chromoendoscopy did not detect more missed adenomas than intensive inspection in this pilot study, larger trials are needed to determine optimal surveillance techniques in this high-risk population.
引用
收藏
页码:470 / 475
页数:6
相关论文
共 50 条
  • [1] Efficacy of Annual Colonoscopic Surveillance in Individuals With Hereditary Nonpolyposis Colorectal Cancer
    Engel, Christoph
    Rahner, Nils
    Schulmann, Karsten
    Holinski-Feder, Elke
    Goecke, Timm O.
    Schackert, Hans K.
    Kloor, Matthias
    Steinke, Verena
    Vogelsang, Holger
    Moeslein, Gabriela
    Goergens, Heike
    Dechant, Stefan
    Doeberitz, Magnus Von Knebel
    Rueschoff, Josef
    Friedrichs, Nicolaus
    Buettner, Reinhard
    Loeffler, Markus
    Propping, Peter
    Schmiegel, Wolff
    CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2010, 8 (02) : 174 - 182
  • [2] Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics
    Robinson, Kristina Lagerstedt
    Liu, Tao
    Vandrovcova, Jana
    Halvarsson, Britta
    Clendenning, Mark
    Frebourg, Thierry
    Papadopoulos, Nickolas
    Kinzler, Kenneth W.
    Vogelstein, Bert
    Peltomaki, Paivi
    Kolodner, Richard D.
    Nilbert, Mef
    Lindblom, Annika
    JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (04) : 291 - 299
  • [3] Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome
    Steinke, Verena
    Engel, Christoph
    Buettner, Reinhard
    Schackert, Hans Konrad
    Schmiegel, Wolff H.
    Propping, Peter
    DEUTSCHES ARZTEBLATT INTERNATIONAL, 2013, 110 (03): : 32 - U28
  • [4] LYNCH SYNDROME (HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER)
    MOYASANZ, A
    GARCIAPASTOR, P
    SENABRE, JJG
    GIMENEZ, FD
    RODERO, DR
    REVISTA ESPANOLA DE ENFERMEDADES DIGESTIVAS, 1994, 86 (05) : 831 - 834
  • [5] Screening for the Lynch syndrome (Hereditary nonpolyposis colorectal cancer).
    Hampel, H
    Frankel, WL
    Martin, E
    Arnold, M
    Khanduja, K
    Kuebler, P
    Nakagawa, H
    Sotamaa, K
    Prior, TW
    Westman, J
    Panescu, J
    Fix, D
    Lockman, J
    Comeras, I
    de la Chapelle, A
    Ellison, C
    Melvin, S
    Winston, J
    Adeli, A
    Burak, W
    Chadwick, R
    Elkhatib, I
    Hemingway, T
    Jamieson, K
    Johnson, C
    LaJeunesse, J
    Liyanarachchi, S
    Rangel, P
    Soble, D
    Walker, M
    Wise, T
    Zhang, Y
    Schlanger, R
    Aguilar, P
    Hura, D
    Keith, J
    Kerner, B
    Lavalle, G
    Taylor, C
    Vara, T
    Zangmeister, J
    DeVictor, S
    Hines, L
    Lindsey, M
    Madhavan, J
    Padmanabhan, A
    Hamelberg, K
    Niemann, T
    Behrens, BC
    Blair, SC
    NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (18): : 1851 - 1860
  • [6] Review article: the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
    Vasen, H. F. A.
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2007, 26 : 113 - 126
  • [7] A century of progress in hereditary nonpolyposis colorectal cancer (Lynch syndrome)
    Thorson, AG
    Knezetic, JA
    Lynch, HT
    DISEASES OF THE COLON & RECTUM, 1999, 42 (01) : 1 - 9
  • [8] Hereditary nonpolyposis colorectal cancer (Lynch syndrome) - An updated review
    Lynch, HT
    Smyrk, T
    CANCER, 1996, 78 (06) : 1149 - 1167
  • [10] RECONSIDERING THE "NON" IN HEREDITARY NONPOLYPOSIS COLORECTAL CANCER: MULTIPLE ADENOMAS DO NOT PRECLUDE LYNCH SYNDROME.
    Kalady, M.
    Kravochuck, S.
    Church, J.
    DISEASES OF THE COLON & RECTUM, 2013, 56 (04) : E238 - E238