Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Clin Cancer Res. 2010 Sep 1;16(17):4374-81. doi: 10.1158/1078-0432.CCR-10-1328. Epub 2010 Aug 24.
The relationship between prostate-specific antigen (PSA) level and prostate cancer risk remains subject to fundamental disagreements. We hypothesized that the risk of prostate cancer on biopsy for a given PSA level is affected by identifiable characteristics of the cohort under study.
We used data from five European and three U.S. cohorts of men undergoing biopsy for prostate cancer; six were population-based studies and two were clinical cohorts. The association between PSA and prostate cancer was calculated separately for each cohort using locally weighted scatterplot smoothing.
The final data set included 25,772 biopsies and 8,503 cancers. There were gross disparities between cohorts with respect to both the prostate cancer risk at a given PSA level and the shape of the risk curve. These disparities were associated with identifiable differences between cohorts: for a given PSA level, a greater number of biopsy cores increased the risk of cancer (odds ratio for >6- versus 6-core biopsy, 1.35; 95% confidence interval, 1.18-1.54; P < 0.0005); recent screening led to a smaller increase in risk per unit change in PSA (P = 0.001 for interaction term) and U.S. cohorts had higher risk than the European cohorts (2.14; 95% confidence interval, 1.99-2.30; P < 0.0005).
Our results suggest that the relationship between PSA and risk of a positive prostate biopsy varies, both in terms of the probability of prostate cancer at a given PSA value and the shape of the risk curve. This poses challenges to the use of PSA-driven algorithms to determine whether biopsy is indicated.
前列腺特异性抗原(PSA)水平与前列腺癌风险之间的关系仍存在根本分歧。我们假设,给定 PSA 水平下前列腺癌的活检风险受研究队列的可识别特征的影响。
我们使用了五个欧洲和三个美国的前列腺癌活检队列的数据;其中六个是基于人群的研究,两个是临床队列。使用局部加权散点平滑法分别计算每个队列中 PSA 与前列腺癌之间的关联。
最终数据集包括 25772 次活检和 8503 例癌症。在给定 PSA 水平下的前列腺癌风险以及风险曲线的形状方面,各队列之间存在明显差异。这些差异与队列之间可识别的差异有关:对于给定的 PSA 水平,更多的活检芯增加了癌症的风险(6 芯与 >6 芯活检的比值比为 1.35;95%置信区间,1.18-1.54;P<0.0005);最近的筛查导致 PSA 每单位变化的风险增加幅度减小(交互项 P=0.001),并且美国队列的风险高于欧洲队列(2.14;95%置信区间,1.99-2.30;P<0.0005)。
我们的结果表明,PSA 与前列腺活检阳性风险之间的关系存在差异,无论是在给定 PSA 值时前列腺癌的概率方面,还是在风险曲线的形状方面。这给基于 PSA 的算法确定是否进行活检带来了挑战。