Mulders T M, Bruning P F, Bonfrer J M
Department of Clinical Oncology, The Netherlands Cancer Institute Antoni van Leeuwenhoekhuis, Amsterdam.
Eur J Surg Oncol. 1990 Feb;16(1):37-41.
Noninvasive methods for the diagnosis of prostatic cancer, its staging and evaluation of response to therapy are often not sufficiently sensitive or specific. Prostate-specific antigen (PSA) was identified in 1979 and has been evaluated since then as a marker, both at the serum and the tissue level. A review is presented in this article. PSA is an organ-specific glycoprotein presented in most prostatic carcinomas, but also in normal prostatic tissue and in benign prostatic hypertrophy (BPH). The monitoring of serum PSA concentrations by serial measurement can be used for the detection of residual or recurrent tumor after primary treatment and for the evaluation of response to systemic treatment of advanced disease. At the tissue level immunohistochemical detection of PSA may help to identify metastatic tumor of unknown origin. PSA serum assays have not been sufficiently sensitive and specific for staging of the primary tumor or for screening purposes. PSA is an equally specific, but more sensitive marker of prostatic carcinoma compared to prostatic acid phosphatase.
用于前列腺癌诊断、分期及评估治疗反应的非侵入性方法通常不够敏感或特异。前列腺特异性抗原(PSA)于1979年被发现,自那时起就作为一种标志物在血清和组织水平进行评估。本文对此进行综述。PSA是一种器官特异性糖蛋白,存在于大多数前列腺癌中,但也存在于正常前列腺组织和良性前列腺增生(BPH)中。通过连续测量监测血清PSA浓度可用于检测初次治疗后残留或复发的肿瘤,以及评估晚期疾病全身治疗的反应。在组织水平,PSA的免疫组化检测可能有助于识别来源不明的转移性肿瘤。PSA血清检测对于原发性肿瘤分期或筛查目的而言,敏感性和特异性均不足。与前列腺酸性磷酸酶相比,PSA是一种同样特异但更敏感的前列腺癌标志物。