4.7 Article

Non-steroidal anti-inflammatory drugs and risk of neoplastic progression in Barretts oesophagus: a prospective study

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LANCET ONCOLOGY
卷 6, 期 12, 页码 945-952

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ELSEVIER SCIENCE INC
DOI: 10.1016/S1470-2045(05)70431-9

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  1. NCI NIH HHS [P01 CA091955, R01 CA61202] Funding Source: Medline
  2. NIEHS NIH HHS [T32 ES07262] Funding Source: Medline

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Background Aspirin and other non-steroidal anti-inflammatory drugs (NSAID) probably decrease the risk of colorectal neoplasia; however their effect on development of oesophageal adenocarcinoma is less dear. We aimed to assess the role of NSAID in the development of oesophageal. adenocarcinoma and precursor lesions in people with Barrett's oesophagus-a metaplastic disorder that confers a high risk of oesophageal adenocarcinoma. Methods We did a prospective study of the relation between duration, frequency, and recency of NSAID use and the risk of oesophageal adenocarcinoma, aneuploidy, and tetraploidy in a cohort of 350 people with Barrett's oesophagus followed for 20 770 person-months. We used proportional-hazards regression to calculate hazard ratios (HR) adjusted for age, sex, cigarette use, and anthropometric measurements. Findings Median follow-up was 65.5 months (range 3.1-106.9). Compared with never users, HR for oesophageal adenocarcinorna (n=37 cases) in current NSAID users was 0.32 (95% CI 0.14-0.76), and in former users was 0.70 (0.31-1.58). 5-year cumulative incidence of oesophageal adenocarcinoma was 14.3% (95% CI 9.3-21.6) for never users, 9.7% (4.-20.5) for former users, and 6.6% (3.1-13.6) for current NSAID users. When changes in NSAID use during follow up were taken into account, the associations were strengthened: HR for oesophageal adenocarcinoma for current users at baseline or afterwards was 0.20 (95% CI 0.10-0.41) compared with never users. Compared with never users, current NSAID users (at baseline and follow-up) had less aneuploidy (n=35 cases; 0.25 [0 12-0.54]) and tetraploidy (n=45 cases; 0.44 [0 22-0-87]). Interpretation NSAID use might be an effective chemopreventive strategy, reducing the risk of neoplastic progression in Barrett's oesophagus.

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