Summary of findings 3. Aromatase inhibitors versus tamoxifen (indirect comparison)a.
Aromatase inhibitors compared with tamoxifen for primary breast cancer prevention (based on network meta‐analysis findings) | ||||||
Patient or population: women with above‐average risk of developing breast cancer Settings: prevention Intervention: aromatase inhibitors Comparison: tamoxifen | ||||||
Outcomes | Illustrative comparative risks* (95% CI) | Relative effect (95% CI) | No of participants (studies) | Certainty of the evidence (GRADE) | Comments | |
Assumed risk | Corresponding risk | |||||
Tamoxifen | Aromatase inhibitors | |||||
Overall breast cancer incidence Follow‐up: 3–16 years |
49 per 1000 | 33 per 1000 ** (23 to 48) |
RR 0.67 (0.46 to 0.98) |
31,256 (5 RCTs) | ⊕⊕⊝⊝ Lowb | — |
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). ** Number needed to treat: 62 CI: confidence interval; RCTs: randomized controlled trial; RR: risk ratio. | ||||||
GRADE Working Group grades of evidence High certainty: further research is very unlikely to change our confidence in the estimate of effect. Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low certainty: we are very uncertain about the estimate. |
aThe findings are from indirect comparison (network meta‐analysis) of two RCTs comparing aromatase inhibitors with placebo and three RCTs comparing tamoxifen with placebo. bDowngraded two levels for partial lack of transitivity and inconsistency.