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基于人群的前列腺癌筛查中前列腺特异性抗原(PSA)升高至4.0纳克/毫升以上的累积概率。

Cumulative probability of PSA increase above 4.0 NG/ML in population-based screening for prostate cancer.

作者信息

Ito Kazuto, Yamamoto Takumi, Ohi Masaru, Takechi Hiroyuki, Kurokawa Kohei, Suzuki Kazuhiro, Yamanaka Hidetoshi

机构信息

Department of Urology, Gunma University School of Medicine, Showa-machi, Maebashi, Gunma, Japan.

出版信息

Int J Cancer. 2004 Apr 10;109(3):455-60. doi: 10.1002/ijc.11711.

Abstract

Routine screening for prostate cancer remains controversial. However, it is very important to show how the optimal rescreening interval should be set for men who want to be screened after informed consent. To solve this issue, the risk of prostate-specific antigen (PSA) increase above 4.0 ng/ml relative to baseline PSA levels and age was investigated. Between 1988 and 2000, 7,757 subjects screened twice or more and also with baseline PSA levels of 4.0 ng/ml or lower were enrolled in our study. All serum PSA levels were measured by E-test Tosoh II PA assay at one center. Interval PSA levels for men undergoing screening with a greater than 1 year interval were calculated on the assumption that PSA levels changed over time in a simple exponential fashion. Then, the cumulative rate of freedom from PSA increase above 4.0 ng/ml was estimated using the Kaplan-Meier technique stratified by baseline PSA ranges of 0.0 to 1.0, 1.1 to 2.0, 2.1 to 3.0 and 3.1 to 4.0 ng/ml and every 10 years of age ranges. Of the 7,757 subjects, 559 (7.2%) were expected to have had PSA levels increase above 4.0 ng/ml within 5 years after the baseline PSA measurements. The cumulative rate of freedom from the PSA increase above 4.0 ng/ml at 5 years was 98.7%, 92.9%, 70.3% and 38.5% in cases of baseline PSA levels of 1.0 ng/ml or lower, 1.1 to 2.0 ng/ml, 2.1 to 3.0 ng/ml and 3.1 to 4.0 ng/ml, respectively. The cumulative rates of freedom from the PSA increase were significantly decreased with the baseline PSA ranges being higher regardless of age range. Re-screening interval should be set stratified by baseline PSA levels, regardless of age and race. Rescreening interval should be set at 1, 1 to 2 and 3 to 5 years for men with baseline PSA ranges of 2.1 to 4.0 ng/ml, 1.1 to 2.0 ng/ml and 0.0 to 1.0 ng/ml, respectively, in individual-based screening. In mass screening system using PSA alone, rescreening interval should be set in the same manner as in individual-based screening, except for men with baseline PSA levels of 1.1 to 2.0 ng/ml, which should be set at 1 year to avoid developing incurable prostate cancer.

摘要

前列腺癌的常规筛查仍存在争议。然而,对于那些在获得知情同意后希望接受筛查的男性,说明应如何设定最佳复查间隔非常重要。为解决这一问题,研究了前列腺特异性抗原(PSA)相对于基线PSA水平升高至4.0 ng/ml以上的风险与年龄的关系。1988年至2000年期间,我们纳入了7757名接受过两次或更多次筛查且基线PSA水平为4.0 ng/ml或更低的受试者。所有血清PSA水平均在一个中心通过E-test Tosoh II PA检测法进行测量。对于筛查间隔大于1年的男性,假设PSA水平随时间呈简单指数方式变化来计算间隔期PSA水平。然后,使用Kaplan-Meier技术,按基线PSA范围0.0至1.0、1.1至2.0、2.1至3.0和3.1至4.0 ng/ml以及每10岁年龄范围进行分层,估计PSA升高至4.0 ng/ml以上的累积无进展率。在7757名受试者中,预计有559名(7.2%)在基线PSA测量后的5年内PSA水平升高至4.0 ng/ml以上。在基线PSA水平为1.0 ng/ml或更低、1.1至2.0 ng/ml、2.1至3.0 ng/ml和3.1至4.0 ng/ml的情况下,5年时PSA升高至4.0 ng/ml以上的累积无进展率分别为98.7%、92.9%、70.3%和38.5%。无论年龄范围如何,随着基线PSA范围升高,PSA升高的累积无进展率均显著降低。复查间隔应根据基线PSA水平进行分层设定,而不考虑年龄和种族。在基于个体的筛查中,对于基线PSA范围为2.1至4.0 ng/ml、1.1至2.0 ng/ml和0.0至1.0 ng/ml的男性,复查间隔应分别设定为1年、1至2年和3至5年。在仅使用PSA的大规模筛查系统中,复查间隔应与基于个体的筛查方式相同,但对于基线PSA水平为1.1至2.0 ng/ml的男性,应设定为1年,以避免发展为无法治愈的前列腺癌。

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