Homma Yukio, Akaza Hideyuki, Okada Kiyoki, Yokoyama Masao, Moriyama Nobuo, Usami Michiyuki, Hirao Yoshihiko, Tsushima Tomoyasu, Sakamoto Atsuhiko, Ohashi Yasuo, Aso Yoshio
Department of Urology, University of Tokyo, Tokyo, Japan.
Int J Urol. 2004 May;11(5):295-303. doi: 10.1111/j.1442-2042.2004.00795.x.
The effects of preoperative androgen deprivation on the outcomes of prostate cancer patients who received radical prostatectomy and subsequent adjuvant endocrine therapy have not yet been fully evaluated.
Patients with stage A(2), B or C prostate cancers were randomized to one of two groups: group I (n = 90), who received androgen deprivation (leuprolide and chlormadinone acetate) for 3 months followed by radical prostatectomy and subsequent adjuvant endocrine therapy (leuprolide alone), and group II (n = 86), who underwent the surgery followed by 3-month androgen deprivation (leuprolide and chlormadinone acetate) and subsequent adjuvant endocrine therapy (leuprolide alone). The effects of preoperative androgen deprivation on survival, clinical relapse (serum prostate specific antigen, PSA, above the normal level, local recurrence, or distant metastases), and PSA relapse (PSA above the detectable level) were evaluated at 5 years or later after treatment.
There were no significant differences in overall, cause-specific, clinical relapse-free, or PSA relapse-free survival rates between the two groups. In a subanalysis, no prostate cancer deaths or clinical relapses were noted in 29 patients with organ-confined disease (OCD: negativity of capsular invasion, seminal vesicle invasion, surgical margins or nodal involvement). The odds ratio for OCD depending on group assignment was 2.44 (95% confidence interval, CI 1.04-5.72), for group I, demonstrating a higher probability of having OCD. This ratio was increased to 4.00 (95% CI 1.06-15.16) if the analysis was conducted in a subpopulation with prostate specific antigen levels less than 35.6 ng/mL and with clinical stage B or C cancers.
Preoperative androgen deprivation has no demonstrable benefit in 5-year outcomes for patients undergoing radical prostatectomy and adjuvant endocrine therapy. However, it did increase the probability of OCD, which was associated with no clinical relapse during the follow-up. A longer observation is needed to clarify the exact extent of the benefits in terms of survival.
术前雄激素剥夺对接受根治性前列腺切除术及后续辅助内分泌治疗的前列腺癌患者预后的影响尚未得到充分评估。
A(2)期、B期或C期前列腺癌患者被随机分为两组:第一组(n = 90),接受3个月的雄激素剥夺治疗(亮丙瑞林和醋酸氯地孕酮),随后进行根治性前列腺切除术及后续辅助内分泌治疗(仅用亮丙瑞林);第二组(n = 86),先进行手术,随后进行3个月的雄激素剥夺治疗(亮丙瑞林和醋酸氯地孕酮)及后续辅助内分泌治疗(仅用亮丙瑞林)。在治疗后5年或更晚时评估术前雄激素剥夺对生存、临床复发(血清前列腺特异性抗原,PSA,高于正常水平、局部复发或远处转移)和PSA复发(PSA高于可检测水平)的影响。
两组在总生存率、病因特异性生存率、无临床复发生存率或无PSA复发生存率方面无显著差异。在一项亚分析中,29例器官局限性疾病(OCD:包膜侵犯、精囊侵犯、手术切缘或淋巴结受累均为阴性)患者未出现前列腺癌死亡或临床复发。根据分组,第一组OCD的优势比为2.44(95%置信区间,CI 1.04 - 5.72),表明患OCD的可能性更高。如果在前列腺特异性抗原水平低于35.6 ng/mL且临床分期为B期或C期癌症的亚组中进行分析,该比值增至4.00(95%CI 1.06 - 15.16)。
术前雄激素剥夺对接受根治性前列腺切除术和辅助内分泌治疗的患者5年预后无明显益处。然而,它确实增加了OCD的可能性,而OCD与随访期间无临床复发相关。需要更长时间的观察来明确在生存获益方面的确切程度。