# Association of alcohol intake over the lifetime with colorectal adenoma and colorectal cancer risk in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial

**Authors:** Caitlin P. O’Connell, Sonja I. Berndt, Kenechukwu Chudy‐Onwugaje, Andrew Kunzmann, Wen‐Yi Huang, Kathryn Hughes Barry, Erikka Loftfield

PMC · DOI: 10.1002/cncr.70201 · Cancer · 2026-01-26

## TL;DR

This study found that heavy alcohol consumption over a lifetime increases the risk of colorectal cancer, especially rectal cancer, while quitting drinking may reduce the risk of adenomas.

## Contribution

The study provides new insights into how lifetime alcohol consumption patterns affect colorectal cancer and adenoma risk.

## Key findings

- Heavy drinkers had a 25% higher risk of colorectal cancer and a 95% higher risk of rectal cancer compared to light drinkers.
- Consistent heavy drinking was associated with a 91% higher risk of colorectal cancer.
- Former drinkers had a 42% lower risk of nonadvanced adenomas compared to current light drinkers.

## Abstract

Alcohol drinking is associated with higher colorectal cancer (CRC) risk, but research on lifetime alcohol drinking is limited. The objective of the current study was to estimate the association of lifetime alcohol drinking with incident colorectal adenoma and cancer.

US adults enrolled in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial reported alcohol intake during four age periods. Average lifetime alcohol intake was calculated as average drinks per week from age 18 years until study baseline. Alcohol intake patterns were defined by past and current drinking frequency. Among 12,327 participants with a negative baseline screen, 812 had an adenoma on the second screen. Logistic regression was used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for incident adenoma. During 20 years of follow‐up, 1679 incident CRC cases occurred among 88,092 participants. Cox proportional hazards regression was used to estimate hazard ratios (HRs) and 95% CIs for CRC.

Current drinkers with an average lifetime alcohol intake of 14 or more drinks per week, compared with one drink or less per week, had a higher risk of CRC (HR, 1.25; 95% CI, 1.01–1.53), especially rectal cancer (HR, 1.95; 95% CI, 1.17–3.28). Consistent heavy drinking versus light drinking was positively associated with CRC risk (HR, 1.91; 95% CI, 1.17–3.12). Compared with current drinkers averaging less than one drink per week, former drinkers had lower odds of nonadvanced adenoma (OR, 0.58; 95% CI, 0.39–0.84). Current drinkers averaging from seven to less than 14 drinks compared with less than one drink per week had a lower risk of CRC (HR, 0.79; 95% CI, 0.64–0.97), especially distal colon cancer (HR, 0.64; 95% CI, 0.42–1.00).

Consistent heavy alcohol intake and higher average lifetime alcohol drinking may increase CRC risk, whereas cessation may lower adenoma risk. Associations may differ by tumor site.

In the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial cohort, participants who drank 14 or more alcoholic drinks per week, compared with those who drank less than one alcoholic drink per week, on average, throughout adulthood, and participants who reported heavy drinking across all age ranges had higher risks of colorectal cancer, especially rectal cancer. Former drinkers had lower odds of nonadvanced adenomas.

## Linked entities

- **Diseases:** colorectal cancer (MONDO:0005575), colorectal adenoma (MONDO:0005484), rectal cancer (MONDO:0006519)

## Full-text entities

- **Diseases:** cancer (MESH:D009369), Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer (MESH:D010051), ulcerative colitis (MESH:D003093), adenoma (MESH:D000236), Gardner syndrome (MESH:D005736), dysplasia (MESH:D015792), carcinogenic (MESH:D011230), Crohn disease (MESH:D003424), familial polyposis (MESH:D011125), colorectal (MESH:D015179), lung (MESH:D008171), PLCO (MESH:D010049), inflammation (MESH:D007249), polyps (MESH:D011127), diabetes (MESH:D003920), colorectal polyp (MESH:D003111), overweight (MESH:D050177), rectal cancer (MESH:D012004), death (MESH:D003643)
- **Chemicals:** -inflammatory drug (-), Acetaldehyde (MESH:D000079), calcium (MESH:D002118), Alcohol (MESH:D000438), folate (MESH:D005492)
- **Species:** Homo sapiens (human, species) [taxon 9606], gut metagenome (species) [taxon 749906]

## Full text

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12833583/full.md

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Source: https://tomesphere.com/paper/PMC12833583