TY - JOUR
T1 - Nonsteroidal anti-inflammatory drugs and statins have chemopreventative effects in patients with Barrett's esophagus
AU - Kastelein, Florine
AU - Spaander, Manon C.W.
AU - Biermann, Katharina
AU - Steyerberg, Ewout W.
AU - Kuipers, Ernst J.
AU - Bruno, Marco J.
PY - 2011/12
Y1 - 2011/12
N2 - Background & Aims: The incidence of Barrett's esophagus and esophageal adenocarcinoma has increased despite surveillance of patients with Barrett's esophagus. Limited data indicate that nonsteroidal anti-inflammatory drug (NSAID) and statin use reduce the risk for esophageal adenocarcinoma. We investigated whether NSAID or statin use reduces the risk of neoplastic progression from Barrett's esophagus. Methods: We performed a prospective study of 570 patients with Barrett's esophagus at 3 academic and 12 regional Dutch hospitals. Information on medication use was collected in patient interviews at each surveillance visit and cross-checked with pharmacy records. Patients completed a questionnaire about use of over-the-counter medication. Incident cases of high-grade dysplasia and adenocarcinoma were identified during the follow-up period. Results: During a median follow-up period of 4.5 years, 38 patients (7%) developed high-grade dysplasia or adenocarcinoma. After Barrett's esophagus had been diagnosed, 318 patients (56%) used NSAIDs for a median duration of 2 months, 161 (28%) used aspirin for a median duration of 5 years, 209 (37%) used statins for a median duration of 5 years, and 107 (19%) used NSAIDs and statins. NSAID and statin use were each associated with a reduced risk of neoplastic progression (hazard ratio [HR], 0.47; P =.030 and HR, 0.46; P =.048, respectively). Use of a combination of NSAIDs and statins increased the protective effect (HR, 0.22; P =.028). Conclusions: NSAID and statin use reduce the risk of neoplastic progression in patients with Barrett's esophagus. Use of a combination of NSAIDs and statins appears to have an additive protective effect.
AB - Background & Aims: The incidence of Barrett's esophagus and esophageal adenocarcinoma has increased despite surveillance of patients with Barrett's esophagus. Limited data indicate that nonsteroidal anti-inflammatory drug (NSAID) and statin use reduce the risk for esophageal adenocarcinoma. We investigated whether NSAID or statin use reduces the risk of neoplastic progression from Barrett's esophagus. Methods: We performed a prospective study of 570 patients with Barrett's esophagus at 3 academic and 12 regional Dutch hospitals. Information on medication use was collected in patient interviews at each surveillance visit and cross-checked with pharmacy records. Patients completed a questionnaire about use of over-the-counter medication. Incident cases of high-grade dysplasia and adenocarcinoma were identified during the follow-up period. Results: During a median follow-up period of 4.5 years, 38 patients (7%) developed high-grade dysplasia or adenocarcinoma. After Barrett's esophagus had been diagnosed, 318 patients (56%) used NSAIDs for a median duration of 2 months, 161 (28%) used aspirin for a median duration of 5 years, 209 (37%) used statins for a median duration of 5 years, and 107 (19%) used NSAIDs and statins. NSAID and statin use were each associated with a reduced risk of neoplastic progression (hazard ratio [HR], 0.47; P =.030 and HR, 0.46; P =.048, respectively). Use of a combination of NSAIDs and statins increased the protective effect (HR, 0.22; P =.028). Conclusions: NSAID and statin use reduce the risk of neoplastic progression in patients with Barrett's esophagus. Use of a combination of NSAIDs and statins appears to have an additive protective effect.
KW - Cancer Risk
KW - Chemoprevention
KW - Gastroesophageal Reflux Disease
KW - Tumor
UR - http://www.scopus.com/inward/record.url?scp=81855167480&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=81855167480&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2011.08.036
DO - 10.1053/j.gastro.2011.08.036
M3 - Article
AN - SCOPUS:81855167480
SN - 0016-5085
VL - 141
SP - 2000
EP - 2008
JO - Gastroenterology
JF - Gastroenterology
IS - 6
ER -