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临床局限性前列腺癌根治性前列腺切除术前新辅助雄激素剥夺治疗的最佳持续时间。

Optimal duration of neoadjuvant androgen withdrawal therapy before radical prostatectomy in clinically confined prostate cancer.

作者信息

Gleave M E, Goldenberg S L, Jones E C, Bruchovsky N, Kinahan J, Sullivan L D

机构信息

Division of Urology, University of British Columbia, Vancouver Hospital, Canada.

出版信息

Semin Urol Oncol. 1996 May;14(2 Suppl 2):39-45; discussion 46-7.

PMID:8725890
Abstract

Experimental studies have shown that neoadjuvant androgen therapy dramatically reduces the rate of local recurrence after tumor excision. In the clinical setting, a 3-month course of neoadjuvant therapy before radical prostatectomy has been shown to significantly reduce positive margin rates, but follow-up is too short to assess the impact of such therapy on biochemical and clinical recurrence rates. A phase II study using an ultrasensitive assay showed that 8 months of neoadjuvant therapy were required before prostate-specific antigen (PSA) levels to reach their nadir in 84% of study participants. The positive margin rate in this study was substantially lower than those reported in the literature. Importantly, restaging of specimens after prostatic acid phosphatase (PAP) immunostaining did not upstage or increase positive margin rates. In addition, prolonged neoadjuvant therapy did not appear to result in progression of androgen-independent clones. A randomized phase III trial has been initiated to determine whether an 8-month course of neoadjuvant hormonal therapy is superior to a 3-month course in reducing positive margin rates and biochemical recurrences in patients with clinically confined prostate cancer.

摘要

实验研究表明,新辅助雄激素治疗可显著降低肿瘤切除术后的局部复发率。在临床实践中,根治性前列腺切除术前行3个月的新辅助治疗已被证明可显著降低切缘阳性率,但随访时间过短,无法评估此类治疗对生化复发率和临床复发率的影响。一项使用超敏检测方法的II期研究表明,84%的研究参与者需要接受8个月的新辅助治疗,前列腺特异性抗原(PSA)水平才能降至最低点。该研究中的切缘阳性率显著低于文献报道。重要的是,前列腺酸性磷酸酶(PAP)免疫染色后标本的重新分期并未使分期升高或增加切缘阳性率。此外,延长新辅助治疗似乎不会导致雄激素非依赖性克隆进展。一项随机III期试验已启动,以确定8个月疗程的新辅助激素治疗在降低临床局限性前列腺癌患者的切缘阳性率和生化复发方面是否优于3个月疗程。

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