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[前列腺特异性抗原在前列腺腺癌诊断与治疗中的作用]

[The role of prostate-specific antigen in the diagnosis and treatment of prostatic adenocarcinoma].

作者信息

Stamey T A

机构信息

Division of Urology, Stanford University.

出版信息

Urologe A. 1990 Mar;29(2):52-64.

PMID:1691883
Abstract

Serum prostate-specific antigen (PSA) levels were determined in four groups of patients with prostatic carcinoma: 230 untreated patients with adenocarcinoma of the prostate after careful clinical staging; in 102 patients with localized prostatic carcinoma who were treated by radical prostatectomy; in 183 patients after radiation therapy for adenocarcinoma of the prostate; and in 45 antiandrogen-treated patients with documented metastatic disease. Within each treatment modality PSA proved to be a powerful tool in predicting stage and prognosis of each patient. In the untreated group the PSA level was directly proportional to advancing clinical stage and Gleason score. The rate of increase of PSA in clinical stage A and B cancer patients suggested a doubling time of at least 2 years. In the group of patients who underwent radical prostatectomy, PSA correlated extremely well with the tumor volume and had a high predictive value for pelvic lymph node metastasis. No patient with pelvic lymph node metastasis achieved an undetectable PSA level following radical prostatectomy without adjunctive therapy. Both anti-androgen and radiation treatment were followed initially by dramatic falls in serum PSA concentrations, but the majority of patients soon experienced a reversal of this initial response, signifying early failure and again providing new information unavailable from any other source.

摘要

对四组前列腺癌患者测定了血清前列腺特异性抗原(PSA)水平:230例经仔细临床分期的未经治疗的前列腺腺癌患者;102例接受前列腺癌根治术治疗的局限性前列腺癌患者;183例接受前列腺腺癌放射治疗后的患者;以及45例接受抗雄激素治疗且有记录的转移性疾病患者。在每种治疗方式中,PSA被证明是预测每位患者分期和预后的有力工具。在未经治疗的组中,PSA水平与临床分期进展和 Gleason评分直接相关。临床A期和B期癌症患者中PSA的升高速率表明其倍增时间至少为2年。在接受前列腺癌根治术的患者组中,PSA与肿瘤体积高度相关,对盆腔淋巴结转移具有较高的预测价值。没有接受辅助治疗的情况下,没有盆腔淋巴结转移的患者在前列腺癌根治术后PSA水平无法检测到。抗雄激素治疗和放射治疗最初都伴随着血清PSA浓度的急剧下降,但大多数患者很快经历了这种初始反应的逆转,这意味着早期失败,并且再次提供了从任何其他来源都无法获得的新信息。

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