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No association between use of phosphodiesterase 5 inhibitors and colorectal cancer in men with erectile dysfunction
Lucía Cea Soriano1,2, Luis A García Rodríguez1
1Spanish Centre for Pharmacoepidemiologic Research (CEIFE), Madrid, Spain.
Purpose:
There is an increase interest on the potential chemoprotective effect of selective phosphodiesterase 5 (PDE5) inhibitors. Several authors have shown in vivo the immune-mediated anti-tumor effect of these inhibitors on tumors arising from the digestive tract.
Objectives:
To test the potential effect of selective PDE5 inhibitors against colorectal cancer (CRC) onset previously observed.
Methods:
We used data from The Health Improvement Network database and identified an established cohort of 200 000 new users of low-dose aspirin and a matched comparison cohort aged 40-84 years between 1 January 2000 and 31 December 2011. A follow-up to identify CRC cases was performed within an extensive validation exercise. Nested case-control analyses compared PDE5 inhibitors vs non-use on CRC risk were performed.
Results:
Restricting to males (59.3% controls and 59.5% cases), no association was observed among current users of PDE5 inhibitors (1.05 [95% CI: 0.69-1.60]) and neither among recent (1.36 [95% CI: 0.81-2.28]) or past users (1.06 [95% CI: 0.72-1.58]). No duration response effect was found.
Conclusions:
Our results do not support an increased risk of CRC associated with the use of PDE5 inhibitors among men with erectile dysfunction.
Insights
This study found no increased risk of colorectal cancer (CRC) associated with phosphodiesterase 5 (PDE5) inhibitor use in men. These findings do not support a link between PDE5 inhibitors and CRC onset in males.
Area of Science:
- Oncology
- Pharmacology
- Epidemiology
Background:
- Selective phosphodiesterase 5 (PDE5) inhibitors are being investigated for potential chemoprotective effects.
- Previous research suggests an immune-mediated anti-tumor effect of PDE5 inhibitors on digestive tract tumors.
Purpose of the Study:
- To evaluate the potential effect of selective PDE5 inhibitors on colorectal cancer (CRC) onset.
- To investigate the association between PDE5 inhibitor use and CRC risk in a large male cohort.
Main Methods:
- A nested case-control study was conducted using data from The Health Improvement Network database.
- A cohort of 200,000 new low-dose aspirin users and a matched comparison group (aged 40-84) were followed from 2000-2011.
- CRC cases were identified and validated; PDE5 inhibitor use (current, recent, past) was compared to non-use.
Main Results:
- Analysis restricted to males showed no significant association between current PDE5 inhibitor use and CRC risk (OR 1.05, 95% CI: 0.69-1.60).
- No increased risk was observed for recent (OR 1.36, 95% CI: 0.81-2.28) or past users (OR 1.06, 95% CI: 0.72-1.58).
- No duration-response effect was detected.
Conclusions:
- The study's findings do not support an increased risk of colorectal cancer associated with PDE5 inhibitor use in men.
- These results suggest that PDE5 inhibitors are not linked to a higher risk of CRC in males with erectile dysfunction.
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