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首页> 外文期刊>Journal of Clinical Oncology >Effect of changing breast cancer incidence rates on the calibration of the Gail model.
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Effect of changing breast cancer incidence rates on the calibration of the Gail model.

机译:乳腺癌发病率变化对盖尔模型校准的影响。

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PURPOSE: The Gail model combines relative risks (RRs) for five breast cancer risk factors with age-specific breast cancer incidence rates and competing mortality rates from the Surveillance, Epidemiology, and End Results (SEER) program from 1983 to 1987 to predict risk of invasive breast cancer over a given time period. Motivated by changes in breast cancer incidence during the 1990s, we evaluated the model's calibration in two recent cohorts. METHODS: We included white, postmenopausal women from the National Institutes of Health (NIH) -AARP Diet and Health Study (NIH-AARP, 1995 to 2003), and the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial (PLCO, 1993 to 2006). Calibration was assessed by comparing the number of breast cancers expected from the Gail model with that observed. We then evaluated calibration by using an updated model that combined Gail model RRs with 1995 to 2003 SEER invasive breast cancer incidence rates. RESULTS: Overall, the Gail model significantly underpredicted the number of invasive breast cancers in NIH-AARP, with an expected-to-observed ratio of 0.87 (95% CI, 0.85 to 0.89), and in PLCO, with an expected-to-observed ratio of 0.86 (95% CI, 0.82 to 0.90). The updated model was well-calibrated overall, with an expected-to-observed ratio of 1.03 (95% CI, 1.00 to 1.05) in NIH-AARP and an expected-to-observed ratio of 1.01 (95% CI: 0.97 to 1.06) in PLCO. Of women age 50 to 55 years at baseline, 13% to 14% had a projected Gail model 5-year risk lower than the recommended threshold of 1.66% for use of tamoxifen or raloxifene but >or= 1.66% when using the updated model. The Gail model was well calibrated in PLCO when the prediction period was restricted to 2003 to 2006. CONCLUSION: This study highlights that model calibration is important to ensure the usefulness of risk prediction models for clinical decision making.
机译:目的:盖尔模型将五个乳腺癌风险因素的相对风险(RR)与特定年龄的乳腺癌发病率和1983年至1987年的监测,流行病学和最终结果(SEER)计划中的竞争性死亡率相结合,以预测罹患乳腺癌的风险。在给定时间段内的浸润性乳腺癌。受1990年代乳腺癌发病率变化的影响,我们在最近的两个队列中评估了该模型的校准。方法:我们纳入了来自美国国立卫生研究院(NIH)-AARP饮食与健康研究(NIH-AARP,1995年至2003年)和前列腺癌,肺癌,结直肠癌和卵巢癌的筛查试验(PLCO,1993年至2007年2006)。通过将盖尔模型中预期的乳腺癌数量与观察到的乳腺癌数量进行比较来评估校准。然后,我们通过使用结合了Gail模型RR和1995年至2003年SEER浸润性乳腺癌发病率的更新模型来评估校准。结果:总体而言,盖尔模型严重低估了NIH-AARP中浸润性乳腺癌的数量,预期与观察的比率为0.87(95%CI,0.85至0.89),而在PLCO中,预期与观察的比率为观察到的比率为0.86(95%CI,0.82至0.90)。更新后的模型在总体上进行了很好的校准,NIH-AARP中的预期与观察比率为1.03(95%CI:1.00至1.05),预期与观察比率为1.01(95%CI:0.97至1.06) )。在基线时年龄为50至55岁的女性中,有13%至14%的Gail模型预计5年风险低于他莫昔芬或雷洛昔芬的推荐阈值1.66%,但使用更新模型时≥1.66%。当预测期限于2003年至2006年时,Gail模型在PLCO中得到了很好的校准。结论:本研究强调模型校准对于确保风险预测模型对临床决策的有效性至关重要。

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