Endoscopic screening for esophageal squamous-cell carcinoma in high-risk patients: a prospective study conducted in 62 french endoscopy centers

被引:95
作者
Dubuc, J.
Legoux, J. -L. [1 ]
Winnock, M.
Seyrig, J. -A.
Barbier, J. -P.
Barrioz, T.
Laugier, R.
Boulay, G.
Grasset, D.
Sautereau, D.
Grigoresco, D.
Butel, J.
Scoazec, J. -Y.
Ponchon, T.
机构
[1] Bordeaux Univ Hosp, Dept Gastroenterol Hepatol, Haut Leveque Hosp, F-33604 Pessac, France
[2] Univ Bordeaux 2, INSERM, U593, F-33076 Bordeaux, France
[3] Gen Hosp, Dept Gastroenterol Hepatol, Pontivy, France
[4] Georges Pompidou European Univ Hosp, Dept Gastroenterol Hepatol, Paris, France
[5] Univ Hosp Poitiers, Dept Gastroenterol Hepatol, Poitiers, France
[6] Timone Univ Hosp, Dept Gastroenterol Hepatol, Marseille, France
[7] Jean Imbert Gen Hosp, Dept Gastroenterol Hepatol, Arles, France
[8] Gen Hosp, Dept Internal Med, Montauban, France
[9] Gen Hosp, Dept Gastroenterol Hepatol, Montauban, France
[10] Univ Hosp Limoges, Dept Gastroenterol Hepatol, Limoges, France
[11] Emile Roux Gen Hosp, Dept Gastroenterol Hepatol, Le Puy En Velay, France
[12] Gen Hosp, Dept Gastroenterol Hepatol, Abbeville, France
[13] Edouard Herriot Univ Hosp, Dept Anat Pathol, Lyon, France
[14] Edouard Herriot Univ Hosp, Dept Gastroenterol Hepatol, Lyon, France
关键词
D O I
10.1055/s-2006-925255
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Study Aims: The prevalence of esophageal squamous-cell carcinoma in high-risk patients and the advantages of systematic Lugol staining during esophagoscopy have not yet been evaluated in a large prospective study. in this study we aimed to assess the prevalence of this type of tumor in high-risk patients, to examine the role of Lugol staining in endoscopic screening for esophageal squamous-cell carcinoma, and to establish whether it is possible to identify a particularly high-risk group which would benefit from systematic screening. Patients and Methods: A prospective study was undertaken in 62 endoscopy centers. A total of 1095 patients were enrolled, none of whom had any esophageal symptoms. These patients had presented with either a past history of or a recent head and neck or tracheobronchial squamous-cell carcinoma (group 1), with alcoholic chronic pancreatitis (group 2), with alcoholic cirrhosis (group 3), or were alcohol and tobacco addicts (group 4). The patients underwent a meticulous endoscopic examination of the esophagus, followed by Lugol staining. Results: The prevalence of esophageal squamous-cell carcinoma was 3.2%. The group 1 patients showed the highest prevalence of carcinoma (5.3%) and the highest prevalence of dysplasia (4.5%). Of the 35 carcinomas detected in the 1095 patients, seven (20%) were early lesions, and 20% were only detected after Lugol staining (P = 0.02). High-grade dysplasia was only observed in group I patients and two-thirds of these lesions were only diagnosed after Lugol staining. The overall prevalence of low-grade dysplasia was 2.4%, and 77% of these were detected only after Lugol staining (P < 0.001). Conclusions: Lugol dye staining increases the sensitivity of esophageal endoscopy for the detection of high-grade dysplasia and cancer. The prevalence of dysplasia and cancer reached 9.9% in group 1, and we therefore believe that an endoscopic screening program could bejustified for patients with head and neck or tracheobronchial cancer.
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页码:690 / 695
页数:6
相关论文
共 27 条
  • [1] Iodine staining for early endoscopic detection of esophageal cancer in alcoholics
    Ban, S
    Toyonaga, A
    Harada, H
    Ikejiri, N
    Tanikawa, K
    [J]. ENDOSCOPY, 1998, 30 (03) : 253 - 257
  • [2] BLOT WJ, 1994, SEMIN ONCOL, V21, P403
  • [3] SUPERFICIAL SQUAMOUS-CELL CARCINOMA OF THE ESOPHAGUS - A REPORT OF 76 CASES AND REVIEW OF THE LITERATURE
    BOGOMOLETZ, WV
    MOLAS, G
    GAYET, B
    POTET, F
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1989, 13 (07) : 535 - 546
  • [4] Fagundes RB, 1999, ENDOSCOPY, V31, P281
  • [5] THE EUROPEAN-EXPERIENCE WITH ESOPHAGEAL CANCER LIMITED TO THE MUCOSA AND SUBMUCOSA
    FROELICHER, P
    MILLER, G
    [J]. GASTROINTESTINAL ENDOSCOPY, 1986, 32 (02) : 88 - 90
  • [6] Fujii T, 1998, INT J ONCOL, V12, P421
  • [7] Hanai A, 1998, JPN J CLIN ONCOL, V28, P54
  • [8] HOLSCHER AH, 1995, CANCER-AM CANCER SOC, V76, P178, DOI 10.1002/1097-0142(19950715)76:2<178::AID-CNCR2820760204>3.0.CO
  • [9] 2-D
  • [10] Inoue H, 2001, ENDOSCOPY, V33, P75