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游离/总前列腺特异性抗原在前列腺癌早期诊断中的价值(105例患者的研究)

[Value of free/total prostate specific antigen in the early diagnosis of prostate cancer (study of 105 patients)].

作者信息

de la Taille A, Houlgatte A, Houdelette P, Berlizot P, Ramirez J, Ricordel I

机构信息

Clinique d'Urologie, Hôpital d'Instruction des Armées du Val de Grâce, Paris, France.

出版信息

Prog Urol. 1997 Apr;7(2):240-5.

PMID:9264766
Abstract

INTRODUCTION

Prostate Specific Antigen (PSA) exists in the serum in several molecular forms which can be measured by immunoradiodetectable assays: free PSA and total PSA (which represent the sum of the free PSA and complexed PSA to alpha 1 antichymotrypsin). Recently, the proportion of free to total PSA could enhance the ability to distinguish benign histologic conditions from cancer.

MATERIAL AND METHODS

Serum samples of 105 patients (31 histologically confirmed prostate cancers and 74 histologically confirmed untreated benign prostatic diseases) were included in this study. The total and free PSA levels were determined using the PSA immunoradioassay of Tandem-R PSA and Tandem - R free PSA.

RESULTS

When all subjects were included, both total PSA and the proportion of free to total PSA significantly differentiated between patients with prostate cancer and patients with benign histologic conditions (p < 0.01 and p < 0.005). However, in men with total PSA values between 4.0 to 10.0 ng/ml, the proportion of free to total PSA significantly differentiated between the patients with benign and malignant histological conditions (p < 0.04). The most interesting was the ability of the proportion of free to total PSA to distinguish patients with total PSA value between 4.0 and 10.0 ng/ml and normal digital examination (p < 0.001). With these values of PSA-T, a free PSA cutoff of 0.23 detected at least 90.4% of cancers and would eliminate 19.4% of negative biopsies.

CONCLUSION

Measurement of the free to total PSA level improves specificity of prostate cancer screening in selected men with elevated total serum PSA levels between 4.0 to 10.0 ng/ml and normal digital examination, and can reduce unnecessary prostate biopsies with minimal effects on the cancer detection rate.

摘要

引言

前列腺特异性抗原(PSA)以多种分子形式存在于血清中,可通过免疫放射检测法进行测量:游离PSA和总PSA(总PSA代表游离PSA与结合至α1抗糜蛋白酶的复合PSA之和)。最近,游离PSA与总PSA的比例能够增强区分良性组织学状况与癌症的能力。

材料与方法

本研究纳入了105例患者的血清样本(31例经组织学确诊的前列腺癌患者和74例经组织学确诊的未经治疗的良性前列腺疾病患者)。使用串联-R PSA和串联-R游离PSA的PSA免疫放射测定法测定总PSA和游离PSA水平。

结果

当纳入所有受试者时,总PSA以及游离PSA与总PSA的比例在前列腺癌患者和良性组织学状况患者之间均有显著差异(p<0.01和p<0.005)。然而,在总PSA值为4.0至10.0 ng/ml的男性中,游离PSA与总PSA的比例在良性和恶性组织学状况患者之间有显著差异(p<0.04)。最有意思的是游离PSA与总PSA的比例能够区分总PSA值在4.0至10.0 ng/ml且直肠指检正常的患者(p<0.001)。对于这些PSA-T值,游离PSA临界值为0.23时可检测出至少90.4%的癌症,并可减少19.4%的阴性活检。

结论

测量游离PSA与总PSA水平可提高对总血清PSA水平在4.0至10.0 ng/ml且直肠指检正常的特定男性进行前列腺癌筛查的特异性,并可减少不必要的前列腺活检,同时对癌症检出率的影响最小。

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