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具有成本效益的前列腺癌检测。减少低收益活检。美国癌症协会国家前列腺癌检测项目的研究人员。

Cost-effective prostate cancer detection. Reduction of low-yield biopsies. Investigators of the American Cancer Society National Prostate Cancer Detection Project.

作者信息

Littrup P J, Kane R A, Mettlin C J, Murphy G P, Lee F, Toi A, Badalament R, Babaian R

机构信息

Wayne State University, School of Medicine, Harper Hospital, Detroit, Michigan.

出版信息

Cancer. 1994 Dec 15;74(12):3146-58. doi: 10.1002/1097-0142(19941215)74:12<3146::aid-cncr2820741214>3.0.co;2-z.

DOI:10.1002/1097-0142(19941215)74:12<3146::aid-cncr2820741214>3.0.co;2-z
PMID:7526969
Abstract

BACKGROUND

In hopes of limiting low-yield prostate biopsies, results of digital rectal examination (DRE), transrectal ultrasound (TRUS), prostate specific antigen (PSA) and age-related PSA values, gland-volume-adjusted PSA levels, and longitudinal PSA changes were analyzed to identify their cost-effectiveness as prognostic indicators in screening, biopsy, and follow-up of patients with prostate cancer.

METHODS

Twenty-nine hundred men with complete data sets from an initial cohort of 2999 men with an annual follow-up for up to 5 years were examined. Intrapatient PSA and gland-volume variability, optimal PSA operating points (o.p.), and test performance scores were determined for each parameter. Decision analysis was then applied retrospectively to each parameter to determine the cancer detection yield, biopsy requirements, and costs for commonly used detection strategies.

RESULTS

For the initial screening decision, the optimal PSA o.p. was 3.0 ng/ml but increased to 5.0 ng/ml in combination with DRE, whereas age-related PSA performed no better than did PSA. The mean intrapatient variability in TRUS gland volume (+5.5 cc) relative to mean volume (34 cc) was 16%, which was less than the 28% (0.64/2.3 ng/ml) relative variability for PSA. For biopsy decisions, using PSA density (PSAD) with a level of 0.12 ng/ml/cc there was no significant difference in accuracy compared with the systematic biopsy of all patients with elevated PSA or age-related PSA levels. Rather than perform systematic biopsy on all patients with PSA levels greater than 4 ng/ml, decision analysis showed that a 16-55% reduction in biopsies could be achieved with a respective cancer loss of 4-25% by limiting biopsy to patients with an increased PSAD level and/or abnormal results of DRE. Using age-related PSA criteria in combination with DRE reduced biopsies by 12% but resulted in minimal cost reductions. The greatest biopsy reduction relative to cancer yield and lowest cost per cancer detected occurred with PSAD-driven biopsy strategies. During follow-up, longitudinal changes in absolute PSA and PSAD levels were significantly better (P < 0.05) than the percentage change in PSA levels per year.

CONCLUSIONS

Cost-effective prostate cancer detection with PSA as a parameter is better achieved if screening and biopsy decisions are not linked intimately. A tailored-biopsy approach for patients with disproportionately elevated PSA levels of suspicious DRE results in the greatest biopsy reduction by selecting lower risk groups for more conservative follow-up.

摘要

背景

为了减少低收益的前列腺活检,对直肠指检(DRE)、经直肠超声(TRUS)、前列腺特异性抗原(PSA)以及年龄相关的PSA值、腺体体积校正后的PSA水平和PSA的纵向变化结果进行分析,以确定它们在前列腺癌患者筛查、活检和随访中作为预后指标的成本效益。

方法

对来自最初2999名男性队列中的2900名有完整数据集且进行了长达5年年度随访的男性进行检查。确定每个参数的患者内PSA和腺体体积变异性、最佳PSA操作点(o.p.)以及检测性能得分。然后对每个参数进行回顾性决策分析,以确定常用检测策略的癌症检测率、活检需求和成本。

结果

对于初始筛查决策,最佳PSA操作点为3.0 ng/ml,但与DRE联合时增至5.0 ng/ml,而年龄相关的PSA并不比PSA表现更好。TRUS腺体体积的患者内平均变异性(+5.5 cc)相对于平均体积(34 cc)为16%,低于PSA的相对变异性28%(0.64/2.3 ng/ml)。对于活检决策,使用PSA密度(PSAD)水平为0.12 ng/ml/cc时,与对所有PSA或年龄相关PSA水平升高的患者进行系统活检相比,准确性无显著差异。决策分析表明,与对所有PSA水平大于4 ng/ml的患者进行系统活检相比,通过将活检限于PSAD水平升高和/或DRE结果异常的患者,活检可减少16 - 55%,相应的癌症漏诊率为4 - 25%。使用年龄相关的PSA标准联合DRE可使活检减少12%,但成本降低极少。相对于癌症检出率,活检减少最多且每检测到一例癌症成本最低的情况发生在PSAD驱动的活检策略中。在随访期间,绝对PSA和PSAD水平的纵向变化显著优于每年PSA水平的百分比变化(P < 0.05)。

结论

如果筛查和活检决策不紧密关联,以PSA为参数进行具有成本效益的前列腺癌检测效果更佳。对于PSA水平不成比例升高或DRE结果可疑的患者,采用量身定制的活检方法,通过选择低风险组进行更保守的随访,可使活检减少最多。

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