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前列腺癌pT3期三联治疗后的长期随访

Long-term follow-up after triple treatment of prostate cancer stage pT3.

作者信息

Schelin Sonny, Madsen Mikael, Palmqvist Elisabeth, Mäkelä Erik, Klintenberg Claes, Aus Gunnar

机构信息

Section of Urology, Department of Surgery, Kalmar County Hospital, Kalmar, Sweden.

出版信息

Scand J Urol Nephrol. 2009;43(3):186-91. doi: 10.1080/00365590902833887.

Abstract

OBJECTIVE

Radical prostatectomy (RP) has become the most common treatment for localized prostate cancer in Sweden. Outcome is extremely good for pT2 stage with Gleason score 6 or less, but more than every fourth operated patient will have a pT3 stage on full amount specimen histology. According to several reports the risk of biochemical recurrence is quite high, especially in stage pT3, on active surveillance after surgery alone. In 1994 the authors recognized this fact at their clinic and decided to apply a new multimodality treatment concept.

MATERIAL AND METHODS

During 10 years, between 1 January 1995 and 1 January 2005, 98 pT3 patients were treated with a triple treatment: 8 months of neoadjuvant/adjuvant luteinizing hormone-releasing hormone (LH-RH) analogue treatment, RP and immediate adjuvant radiotherapy (RT) 3 months after RP. RT was delivered to 60 Gy in 30 fractions to the prostatic bed to all the patients. The cumulative risk of progression was calculated with the Kaplan-Meier method. The impact of risk factors was evaluated by the Cox proportional hazard model.

RESULTS

Ninety-eight (74 pT3a and 24 pT3b) patients were followed with a mean observation time from operation until October 2007 of 71.6 (median 65.5, range 35-146) months. The mean follow-up time to biochemical failure, death or last measurement of prostate-specific antigen (PSA) was 57.8 (median 57.0, range 3-132) months. Fifteen patients out of 98 had experienced biochemical failure. Only Gleason score had an independent impact on the risk of PSA progression. Complications were mild and temporary and no serious adverse events were registered.

CONCLUSIONS

Patients with locally advanced prostate cancer have a high risk of progression after RP as single therapy. Postoperative RT has been shown to improve the outcome. Neoadjuvant/adjuvant hormonal therapy has been shown to improve the outcome after RT. Bringing this knowledge together offering a multimodality therapy with neoadjuvant/adjuvant hormonal therapy, RP followed by postoperative immediate RT seems to offer a high chance of biochemical-free survival.

摘要

目的

根治性前列腺切除术(RP)已成为瑞典局限性前列腺癌最常见的治疗方法。对于 Gleason 评分 6 分及以下的 pT2 期患者,治疗效果极佳,但在完整标本组织学检查中,每四名接受手术的患者中就有超过一名会出现 pT3 期。根据几份报告,生化复发风险相当高,尤其是在 pT3 期,仅术后进行主动监测时。1994 年,作者在其诊所认识到这一事实,并决定应用一种新的多模式治疗理念。

材料与方法

在 1995 年 1 月 1 日至 2005 年 1 月 1 日的 10 年间,98 例 pT3 期患者接受了三联治疗:8 个月的新辅助/辅助促性腺激素释放激素(LH-RH)类似物治疗、RP 以及 RP 后 3 个月立即进行辅助放疗(RT)。所有患者的前列腺床均接受 30 次分割、总剂量 60 Gy 的 RT。采用 Kaplan-Meier 方法计算累积进展风险。通过 Cox 比例风险模型评估风险因素的影响。

结果

98 例(74 例 pT3a 和 24 例 pT3b)患者接受随访,从手术到 2007 年 10 月的平均观察时间为 71.6(中位数 65.5,范围 35 - 146)个月。至生化失败、死亡或最后一次前列腺特异性抗原(PSA)测量的平均随访时间为 57.8(中位数 57.0,范围 3 - 132)个月。98 例患者中有 15 例经历了生化失败。只有 Gleason 评分对 PSA 进展风险有独立影响。并发症轻微且为暂时性,未记录到严重不良事件。

结论

局部晚期前列腺癌患者接受单一 RP 治疗后进展风险较高。术后放疗已被证明可改善治疗效果。新辅助/辅助激素治疗已被证明可改善放疗后的治疗效果。综合这些知识,提供一种新辅助/辅助激素治疗、RP 后立即进行术后放疗的多模式治疗似乎提供了高无生化复发生存机会。

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