Detection of prostate cancer
Detection of prostate cancer
复制标题
前列腺癌的检测
DOI:
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发表时间:
1995
影响因子:
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通讯作者:
Fritz H Schroder
中科院分区:
文献类型:
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作者:
Fritz H Schroder
Screening the whole population has not yet been shown to be worth while
In August 1994 the United States Food and Drug Administration approved a blood test for use in detecting cancer of the prostate. The Hybritech Tandem assays for prostate specific antigen were recommended for use in combination with digital rectal examination. The decision was based on data from detection studies—but mainly on a recent study of 6630 men carried out in six different centres by Catalona et al.1 Clearly prostate cancer can be detected earlier and at a higher rate when this combination of tests is used. The study group concluded that “the majority of prostate cancers have spread beyond the gland when first diagnosed using the conventional detection method, digital rectal examination. With no curative therapy for advanced prostate cancer available currently or in the foreseeable future, the most promising alternative for improving the prognosis of patients is to enhance early detection.” The report went on to claim that the test improved the detection of prostate cancer confined to the gland by as much as 78% over conventional rectal examination. The proportion of cancers confined to the prostate in the 114 men who underwent surgical treatment by radical prostatectomy was 71%—an important improvement over earlier studies such as that by Van den Ouden et …