首页> 外文期刊>Ultrasound quarterly. >Should prostate-specific antigen or prostate-specific antigen density be used as the determining factor when deciding which prostates should undergo biopsy during prostate ultrasound.
【24h】

Should prostate-specific antigen or prostate-specific antigen density be used as the determining factor when deciding which prostates should undergo biopsy during prostate ultrasound.

机译:在确定哪些前列腺应该在前列腺超声检查期间进行活检时,应使用前列腺特异性抗原或前列腺特异性抗原密度作为决定因素。

获取原文
获取原文并翻译 | 示例
       

摘要

Prostate ultrasound has been accepted as the appropriate tool for prostate biopsy guidance to determine the presence of prostate cancer if the prostate-specific antigen (PSA) level is not normal. Prostate-specific antigen density (PSAD) has been used to determine if an increased PSA level may be because of benign enlargement of the gland or possible presence of cancer. The specific "cutoff" for PSA and PSAD to delineate which patients are at highest risk has been controversial. We attempted to assess which PSA level or PSAD level should be used. A retrospective analysis of 600 consecutive men, referred for prostate ultrasound and possible biopsy because of an abnormal DRE result or increased PSA level was undertaken. All had prostate volume determined by biplanar endorectal ultrasound. One hundred sixty-six men had cancer confirmed by biopsy. This latter group was further analyzed and was divided into PSA <4.0, PSA 4 to 10, or PSA >10.0 ng/ml. Groups were divided according to those with PSAD <0.10, <0.12, and <0.15 ng/ml. Correlation with Gleason grade of the tumor was made. Of the 166 men with cancer, 15 had PSA levels <4 ng/ml (all palpable), and 81 had PSA levels between 4.0 and 10.0 ng/ml (48 were not palpable by digital rectal examination [DRE]). There were 38 (22.8%) of 166 men with cancer who had a PSAD <0.15. Using the Gleason scoring system, 30 of 38 men had mid-grade or high-grade cancers. Twenty-one (12.6%) of 166 men with cancer had a PSAD <0.12. Of these, 17 of 21 men had mid-grade or high-grade cancers. Fifteen (9.0%) of 166 men with cancer had a PSAD <0.10. Of these, 13 of 15 had mid-grade or high-grade cancer. If the PSA level is more than 4.0 ng/ml, even if no palpable lesion is discerned by DRE, suspicion for the presence of cancer should be raised. The use of PSAD threshold of 0.15 is not inclusive enough to identify clinically important cancer, and it should not be used. Our data demonstrate that 7.9% of men with cancer had a PSAD <0.15 and mid-grade or high-grade, i.e., clinically important, cancer. Although more negative biopsy results will be obtained, we recommend the use of a lower PSAD cutoff with PSA levels more than 4 ng/ml and a PSAD higher than 0.10 should undergo a prostate biopsy to detect clinically important cancer.
机译:如果前列腺特异性抗原(PSA)水平不正常,则前列腺超声已被认为是指导前列腺穿刺活检以确定前列腺癌存在的合适工具。前列腺特异性抗原密度(PSAD)已用于确定PSA水平升高是否是由于腺体良性增大或可能存在的癌症所致。具体的“截止”为PSA和PSAD划定哪些患者最危险一直存在争议。我们试图评估应该使用哪个PSA级别或PSAD级别。回顾性分析了600名连续男性,由于异常DRE结果或PSA水平升高而进行了前列腺超声检查和可能的活检。所有患者的前列腺体积均通过双平面直肠内超声确定。 166名男性经活检证实患有癌症。后一组进一步分析,分为PSA <4.0,PSA 4至10或PSA> 10.0 ng / ml。根据PSAD <0.10,<0.12和<0.15 ng / ml的组进行分组。建立了与肿瘤的格里森分级的相关性。在166名癌症男性中,有15名PSA水平<4 ng / ml(全部可触知),有81名PSA水平在4.0至10.0 ng / ml之间(数字直肠检查[DR​​E]无法测出48位)。 166名癌症男性中有38名(22.8%)的PSAD <0.15。使用格里森评分系统,在38名男性中,有30名患有中度或高级癌症。 166名癌症患者中有21名(12.6%)的PSAD <0.12。其中,在21名男性中,有17名患有中度或高级癌症。 166名癌症患者中有15名(9.0%)的PSAD <0.10。在这些患者中,有15个中的13个患有中度或高级癌症。如果PSA水平超过4.0 ng / ml,即使DRE不能识别出明显的病变,也应提高对癌症存在的怀疑。 PSAD阈值0.15的使用不足以识别临床上重要的癌症,因此不应使用。我们的数据表明,有7.9%的癌症患者的PSAD <0.15,且属于中级或高级,即临床上重要的癌症。尽管将获得更多的阴性活检结果,但我们建议使用PSA浓度大于4 ng / ml的较低PSAD截止值和大于0.10的PSAD进行前列腺活检以检测具有临床意义的癌症。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号