4.8 Article

Effect of aspirin and NSAIDs on risk and survival from colorectal cancer

Journal

GUT
Volume 59, Issue 12, Pages 1670-U114

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/gut.2009.203000

Keywords

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Funding

  1. Cancer Research UK [C348/A3758, C348/A8896, C31250/A10107, C26031/A11378]
  2. Scottish government Chief Scientist Office [K/OPR/2/2/D333, CZB/4/94]
  3. Medical Research Council [G0000657-53203]
  4. CORE
  5. MRC [MC_U127527198] Funding Source: UKRI
  6. Cancer Research UK [11378] Funding Source: researchfish
  7. Chief Scientist Office [CZB/4/449] Funding Source: researchfish
  8. Medical Research Council [MC_U127527198] Funding Source: researchfish

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Background Previous studies have shown that aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) lower colorectal cancer (CRC) risk. However, the lowest effective NSAID dose, treatment duration, and effects on survival are not defined. In a large population-based case-control study, we have explored the relationship between NSAID dose and duration, CRC risk and overall CRC-specific survival. Methods The relationship between NSAID use and CRC risk was examined in 2279 cases and 2907 controls. Subjects completed food-frequency and lifestyle questionnaires. NSAID categories were low-dose aspirin (75 mg), non-aspirin NSAIDs (NA-NSAIDs) and any NSAID. Users were defined as taking >4 tablets/week for >1 month. ORs were calculated by logistic regression models and adjusted for potential confounding factors. Effect of NSAID use on all-cause and CRC-specific mortality was estimated using Logrank tests and Cox's hazard models. Results In all, 354 cases (15.5%) were taking low-dose aspirin compared to 526 controls (18.1%). Low-dose aspirin use was associated with decreased CRC risk (OR 0.78 95% CI 0.65 to 0.92, p=0.004), evident after 1 year and increasing with duration of use (p(trend)=0.004). NA-NSAID and any NSAID use were also inversely associated with CRC. There was no demonstrable effect of NSAIDS on all-cause (HR 1.11, p=0.22, 0.94-1.33) or CRC-specific survival (HR 1.01, p=0.93, 0.83-1.23). Conclusion This is the first study to demonstrate a protective effect against CRC associated with the lowest dose of aspirin (75 mg per day) after only 5 years use in the general population. NSAID use prior to CRC diagnosis does not influence survival from the disease.

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