Evidence from randomized controlled trials suggests that calcium may protect against recurrence of colorectal adenomas, which could lead to the subsequent prevention of cancer. Yet the trials used only a large single dose and were of small sizes, and thus, knowledge of the dose-response relationship and influence on high-risk adenomas is limited. To address these issues, we conducted linear and nonlinear dose-response meta-analyses primarily based on prospective observational studies published up to July 2014 identified from PubMed and Embase. Summary relative risks (RRs) and 95% confidence intervals (CIs) were calculated for total and supplemental calcium intake, respectively, using a random-effects model. For total calcium intake, summary RR for each 300 mg/day increase was 0.95 (95% CI 5 0.92-0.98; I 2 5 45%; eight studies with 11,005 cases;range of intake 5 333-2,229 mg/day). Evidence of nonlinearity was indicated: approximately, compared to 550 mg/day of total calcium intake, the summary RR was 0.92 (95% CI 5 0.89-0.94) at 1,000 mg/day and 0.87 (95% CI 5 0.84-0.90) at 1,450 mg/day (p nonlinearity < 0.01). Associations were stronger for high-risk adenomas (1 cm in diameter, (tubulo)villous histology, dysplasia, or multiplicity): approximately, compared to 550 mg/day of total calcium intake, the summary RR was 0.77 (95% CI 5 0.74-0.81) at 1,000 mg/day and reduced to 0.69 (95% CI 5 0.66-0.73) at 1,450 mg/da (p nonlinearity < 0.01). For supplemental calcium intake, summary RR of total adenoma risk for each 300 mg/day increase was 0.96 (95% CI 5 0.93-0.99; I 2 5 0%; three studies with 4,548 cases; range of supplementation 5 0-1,366 mg/day). In conclusion, calcium intake may continue to decrease the risk of adenomas, particularly high-risk adenomas, over a wide range of calcium intake.