Monitoring of total and free prostate-specific antigen, neuroendocrine markers and testosterone in patients with localised-prostate cancer treated by brachytherapy or conformal radiotherapy

被引:1
|
作者
Hersant, A. -M. [1 ]
Galinat, H. [1 ]
Breton-Callu, C. [2 ]
Mortazavi, N. [1 ]
Floiras, J. -L. [2 ]
Pichon, M. -F. [1 ]
机构
[1] Ctr Rene Huguenin Lutte Contre Canc, Lab Oncobiol, F-92210 St Cloud, France
[2] Ctr Rene Huguenin Lutte Contre Canc, Serv Radiotherapie, F-92210 St Cloud, France
来源
IMMUNO-ANALYSE & BIOLOGIE SPECIALISEE | 2008年 / 23卷 / 06期
关键词
Total and free PSA; Chromogranin A; NSE; Prostate cancer; Radiotherapy;
D O I
10.1016/j.immbio.2008.07.014
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Localised prostate-cancer patients treated by brachytherapy (CT, n= 57) or conformal external beam radiotherapy (RTE, n=47) were followed before, during and after radiotherapy, with serial assays of total PSA (tPSA), free PSA (fPSA), chromogranin A (CgA), neuron-specific enolase (NSE) and testosterone. During follow-up (median: 5.3 years), five biological. failures, 10 local recurrences and five metastases were recorded. Overall, tPSA and fPSA concentrations were correlated (n=740), together with nadir tPSA and fPSA concentrations and times to nadir (n=104), all with p<0.0001. In patients without neoadjuvant-hormone therapy (n=75), tPSA half-life was 97 days (range: eight to 360 days) for CT patients and 113 days (range: 29 to 358 days) for RTE patients (nonsignificant difference). Neoadjuvant treatment resulted in a shortened tPSA half-life and a lower tPSA nadir reached in a shorter time. Serum CgA was more elevated in Gleason >= 6 tumours than in the opposite group (p=0.012). (C) 2008 Elsevier Masson SAS. Tous droits reserves.
引用
收藏
页码:379 / 385
页数:7
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