Program in Biostatistics, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Department of Biostatistics, University of Washington, Seattle, Washington.
Cancer. 2018 Apr 15;124(8):1752-1759. doi: 10.1002/cncr.31253. Epub 2018 Jan 25.
Racial disparities in prostate cancer survival (PCS) narrowed during the prostate-specific antigen (PSA) era, suggesting that screening may induce more equitable outcomes. However, the effects of lead time and overdiagnosis can inflate survival even without real screening benefit.
A simulation model of PCS in the early PSA era (1991-2000) was created. The modeled survival started with baseline survival in the pre-PSA era (1975-1990) and added lead times and overdiagnosis using estimates from published studies. The authors quantified 1) discrepancies between modeled and observed PCS in the PSA era and 2) residual period effects on PCS given specified values for screening benefit.
Lead time and overdiagnosis explained more of the improvement in PCS for older ages at diagnosis (46% [95% confidence interval (CI), 44%-50%] for blacks and 51% [95% CI, 50%-52%] for all races ages 50-54 years vs 98% [95% CI, 97%-99%] for blacks and 100% for all races ages 75-79 years). They also explained more of the narrowing in PCS disparities for older ages (33% [95% CI, 31%-43%] for men ages 50-54 years vs 74% [95% CI, 71%-81%] for men ages 75-79 years). The period effects amounted to reductions of 27% to 40% among blacks and 26% to 38% among all races in the risk of prostate cancer death, depending on the screening benefit.
Real improvements in survival disparities in the PSA era are smaller than those observed and reflect similar reductions in the risk of prostate cancer death among blacks and all races. Understanding screening artifacts is necessary for valid interpretation of observed survival trends. Cancer 2018;124:1752-9. © 2018 American Cancer Society.
在前列腺特异性抗原(PSA)时代,前列腺癌生存(PCS)的种族差异缩小,这表明筛查可能带来更公平的结果。然而,领先时间和过度诊断的影响即使没有真正的筛查益处,也会使生存数据膨胀。
建立了 PSA 早期时代(1991-2000 年)PCS 的模拟模型。建模生存从 PSA 时代之前(1975-1990 年)的基线生存开始,并使用已发表研究的估计值添加领先时间和过度诊断。作者量化了 1)PSA 时代模型化和观察到的 PCS 之间的差异,以及 2)在指定筛查益处值的情况下对 PCS 的剩余时期影响。
领先时间和过度诊断解释了更多的 PCS 改善,这些改善发生在诊断时年龄较大的人群中(46%[95%置信区间(CI),44%-50%]为黑人,51%[95%CI,50%-52%]为所有种族 50-54 岁年龄组,而 98%[95%CI,97%-99%]为黑人,所有种族 75-79 岁年龄组 100%)。它们还解释了更大的 PCS 种族差异缩小(33%[95%CI,31%-43%]为 50-54 岁年龄组男性,74%[95%CI,71%-81%]为 75-79 岁年龄组男性)。取决于筛查益处,黑人的前列腺癌死亡风险降低了 27%至 40%,所有种族的风险降低了 26%至 38%。
PSA 时代生存差异的真实改善小于观察到的改善,反映了黑人与所有种族之间前列腺癌死亡风险的相似降低。了解筛查伪影对于正确解释观察到的生存趋势是必要的。癌症 2018;124:1752-9. © 2018 美国癌症协会。