Hormono-radiotherapy in prostatic carcinoma:: Prognostic factors and implications for combined modality treatment

被引:1
|
作者
Cellini, N
Luzi, S
Morganti, AG [1 ]
Mantini, G
Valentini, V
Racioppi, M
Leone, M
Mattiucci, GC
Di Gesù, C
Giustacchini, M
Destito, A
Smaniotto, D
Alcini, E
机构
[1] Univ Cattolica Sacro Cuore, Policlin A Gemelli, Ist Radiol,Cattedra Radioterapia, Unita Operativa Radioterapia, I-86100 Campobasso, Italy
[2] Univ Cattolica Sacro Cuore, Policlin A Gemelli, Ist Clin Chirurg, Cattedra Urol, I-86100 Campobasso, Italy
关键词
combined therapy; hormonotherapy; prognostic factors; prostate carcinoma; radiotherapy;
D O I
10.1177/030089160208800612
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to evaluate the prognostic role of several clinical variables in a patient population undergoing neoadjuvant hormonotherapy (NHT) with external beam radiotherapy (ERT) to identify subsets of patients with an unfavorable prognosis who require intensified therapy. Eighty-four patients (mean age, 68.2 +/- 6.1 years; range, 52-81 years) underwent ERT (45 Gy to pelvic volume; 65 Gy mean dose to prostate volume) and NHT (oral flutamide: 250 mg three times daily for 30 days; LH-RH analogue: one vial every 28. days starting two months before radiotherapy and for its entire duration). The distribution according to clinical stage was T2: 46.4%, T3: 50.0%, T4: 3.6%. The distribution according to the Gleason score was grade 2-4: 17.9%; grade 5-7: 53.6%; grade 8-10: 28.5%. The distribution according to pretreatment PSA levels (in ng/mL) was 0-4:5.9%; 4-10:26.2%; 10-20:16.7%; greater than or equal to20: 51.2%. With a median follow-up of 36 months, 3.6% of patients died; hernatogenous metastases and local disease progression were found in 16.7% and 6% of patients, respectively. Overall, the incidence of disease progression was 17.9%. 32.9% of patients showed biochemical failure during follow-up. Overall, metastasis-free, local progression-free and biochemical failure-free actuarial survival at five years was 89.2%, 66.5%, 85.0% and 41.9%, respectively. At univariate analysis (log-rank) clinical stage (cT) was shown to be significantly correlated with the incidence of metastasis (P = 0.0004), local progression (P <0.0001) and disease-free survival (P = 0.0005). At multivariate analysis (Cox) the correlations between clinical stage and metastasis (P = 0.0175), local progression (P = 0.0200) and disease-free survival (P = 0.0175) were confirmed. Gleason score and pretreatment PSA levels did not show any significant correlation with these endpoints. These results confirm the indications of the recent literature, which, in prostate carcinoma at higher clinical stages, suggest the use of prolonged hormonal therapy after radiotherapy.
引用
收藏
页码:495 / 499
页数:5
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