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加拿大国家乳房筛查研究中浸润性乳腺癌进展的参数估计。

Parameter estimates for invasive breast cancer progression in the Canadian National Breast Screening Study.

机构信息

Department of Mechanical and Industrial Engineering, Ryerson University, Toronto, ON M5B 2K3, Canada.

出版信息

Br J Cancer. 2013 Feb 19;108(3):542-8. doi: 10.1038/bjc.2012.596. Epub 2013 Jan 15.

Abstract

BACKGROUND

The aim of screening is to detect a cancer in the preclinical state. However, a false-positive or a false-negative test result is a real possibility.

METHODS

We describe invasive breast cancer progression in the Canadian National Breast Screening Study and construct progression models with and without covariates. The effect of risk factors on transition intensities and false-negative probability is investigated. We estimate the transition rates, the sojourn time and sensitivity of diagnostic tests for women aged 40-49 and 50-59.

RESULTS

Although younger women have a slower transition rate from healthy state to preclinical, their screen-detected tumour becomes evident sooner. Women aged 50-59 have a higher mortality rate compared with younger women. The mean sojourn times for women aged 40-49 and 50-59 are 2.5 years (95% CI: 1.7, 3.8) and 3.0 years (95% CI: 2.1, 4.3), respectively. Sensitivity of diagnostic procedures for older women is estimated to be 0.75 (95% CI: 0.55, 0.88), while women aged 40-49 have a lower sensitivity (0.61, 95% CI: 0.42, 0.77). Age is the only factor that affects the false-negative probability. For women aged 40-49, 'age at entry', 'history of breast disease' and 'families with breast cancer' are found to be significant for some of the transition rates. For the age-group 50-59, 'age at entry', 'history of breast disease', 'menstruation length' and 'number of live births' are found to affect the transition rates.

CONCLUSION

Modelling and estimating the parameters of cancer progression are essential steps towards evaluating the effectiveness of screening policies. The parameters include the transition rates, the preclinical sojourn time, the sensitivity, and the effect of different risk factors on cancer progression.

摘要

背景

筛查的目的是在临床前期检测癌症。然而,假阳性或假阴性的检测结果是真实存在的可能性。

方法

我们描述了加拿大国家乳房筛查研究中的浸润性乳腺癌进展,并构建了有和没有协变量的进展模型。研究了风险因素对转移强度和假阴性概率的影响。我们估计了 40-49 岁和 50-59 岁女性的转移率、逗留时间和诊断测试的敏感性。

结果

尽管年轻女性从健康状态向临床前期的转移率较慢,但她们的筛查检测到的肿瘤更早出现。50-59 岁女性的死亡率高于年轻女性。40-49 岁和 50-59 岁女性的平均逗留时间分别为 2.5 年(95%CI:1.7,3.8)和 3.0 年(95%CI:2.1,4.3)。估计老年女性诊断程序的敏感性为 0.75(95%CI:0.55,0.88),而 40-49 岁女性的敏感性较低(0.61,95%CI:0.42,0.77)。年龄是唯一影响假阴性概率的因素。对于 40-49 岁的女性,“进入年龄”、“乳房疾病史”和“乳腺癌家族史”被发现对某些转移率有重要影响。对于 50-59 岁的女性,“进入年龄”、“乳房疾病史”、“月经周期长度”和“活产数”被发现影响转移率。

结论

对癌症进展的参数进行建模和估计是评估筛查政策有效性的重要步骤。这些参数包括转移率、临床前期逗留时间、敏感性以及不同风险因素对癌症进展的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1877/3593551/53a6178043ed/bjc2012596f1.jpg

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