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根治性放疗联合长期雄激素剥夺治疗局部进展期前列腺癌患者行全盆腔放疗的效果。

Effect of whole pelvic radiotherapy for patients with locally advanced prostate cancer treated with radiotherapy and long-term androgen deprivation therapy.

机构信息

Department of Radiotherapy, Policlinico Universitario A. Gemelli, Catholic University, Rome, Italy.

出版信息

Int J Radiat Oncol Biol Phys. 2011 Dec 1;81(5):e721-6. doi: 10.1016/j.ijrobp.2010.12.003. Epub 2011 Jan 27.

Abstract

PURPOSE

To evaluate the effect of whole pelvic radiotherapy (WPRT) in prostate cancer patients treated with RT and long-term (>1 year) androgen deprivation therapy (ADT).

METHODS AND MATERIALS

Prostate cancer patients with high-risk features (Stage T3-T4 and/or Gleason score≥7 and/or prostate-specific antigen level≥20 ng/mL) who had undergone RT and long-term ADT were included in the present analysis. Patients with bowel inflammatory disease, colon diverticula, and colon diverticulitis were excluded from WPRT and treated with prostate-only radiotherapy (PORT). Patients were grouped according to nodal risk involvement as assessed by the Roach formula using different cutoff levels (15%, 20%, 25%, and 30%). Biochemical disease-free survival (bDFS) was analyzed in each group according to the RT type (WPRT or PORT).

RESULTS

A total of 358 patients treated between 1994 and 2007 were included in the analysis (46.9% with WPRT and 53.1% with PORT). The median duration of ADT was 24 months (range, 12-38). With a median follow-up of 52 months (range, 20-150), the overall 4-year bDFS rate was 90.5%. The 4-year bDFS rate was similar between the patients who had undergone WPRT or PORT (90.4% vs. 90.5%; p=NS). However, in the group of patients with the greatest nodal risk (>30%), a significant bDFS improvement was recorded for the patients who had undergone WPRT (p=.03). No differences were seen in acute toxicity among the patients treated with WPRT or PORT. The late gastrointestinal toxicity was similar in patients treated with PORT or WPRT (p=NS).

CONCLUSIONS

Our analysis has supported the use of WPRT in association with long-term ADT for patients with high-risk nodal involvement (>30%), although a definitive recommendation should be confirmed by a randomized trial.

摘要

目的

评估接受放疗(RT)和长期(>1 年)雄激素剥夺治疗(ADT)的前列腺癌患者进行全盆腔放疗(WPRT)的效果。

方法和材料

本分析纳入了高风险特征(T3-T4 期和/或 Gleason 评分≥7 和/或前列腺特异性抗原水平≥20ng/ml)接受 RT 和长期 ADT 的前列腺癌患者。患有肠道炎性疾病、结肠憩室和结肠炎的患者被排除在 WPRT 之外,仅接受前列腺放疗(PORT)。根据 Roach 公式评估的淋巴结风险受累情况,将患者分为不同的截定点(15%、20%、25%和 30%)。根据 RT 类型(WPRT 或 PORT),分析每组的生化无病生存(bDFS)。

结果

共纳入 1994 年至 2007 年间治疗的 358 例患者(46.9%接受 WPRT,53.1%接受 PORT)。ADT 的中位持续时间为 24 个月(范围 12-38)。中位随访 52 个月(范围 20-150),总体 4 年 bDFS 率为 90.5%。接受 WPRT 或 PORT 的患者 4 年 bDFS 率相似(90.4%与 90.5%;p=NS)。然而,在淋巴结风险最高的患者组(>30%),接受 WPRT 的患者 bDFS 显著改善(p=.03)。接受 WPRT 或 PORT 治疗的患者之间急性毒性无差异。PORT 或 WPRT 治疗的患者晚期胃肠道毒性相似(p=NS)。

结论

我们的分析支持将 WPRT 与长期 ADT 联合用于高淋巴结风险(>30%)患者,尽管需要随机试验来证实这一明确建议。

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