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前列腺癌质子调强放疗的 II 期临床研究。

A phase II study of hypofractionated proton therapy for prostate cancer.

机构信息

Research Institute and Hospital, National Cancer Center, Goyang, Korea.

出版信息

Acta Oncol. 2013 Apr;52(3):477-85. doi: 10.3109/0284186X.2013.764011. Epub 2013 Feb 11.

Abstract

BACKGROUND

Hypofractionated radiotherapy potentially offers therapeutic gain for prostate cancer. We investigated the feasibility of hypofractionated proton therapy (PT).

MATERIAL AND METHODS

Eighty-two patients with biopsy-proven T1-3N0M0 prostate adenocarcinoma and no history of androgen deprivation therapy were randomly assigned to five different dose schedules: Arm 1, 60 CGE (cobalt gray equivalent = proton dose in Gy × 1.1)/20 fractions/5 weeks; Arm 2, 54 CGE/15 fractions/5 weeks; Arm 3, 47 CGE/10 fractions/5 weeks; Arm 4, 35 CGE/5 fractions/2.5 weeks; or Arm 5, 35 CGE/5 fractions/5 weeks.

RESULTS

The median follow-up duration was 42 months (11-52 months). The acute GI and GU grade ≥ 2 toxicity rates were 0 and 5%, respectively. The late GI and GU grade ≥ 2 toxicity rates were 16% and 7%, respectively. The best arm for acute GU toxicity was Arm 3, while that for late GI toxicity was Arm 2 in which none had grade ≥ 2 toxicity. The four-year American Society for Therapeutic Radiology and Oncology and Nadir + 2ng/ml BCF free survival (BCFFS) rates were 85% and 86%, respectively.

CONCLUSIONS

Hypofractionated PT for patients with prostate adenocarcinoma as used in this study is feasible with an acceptable toxicity profile. As the BCFFS rates do not seem to be inferior to those produced using conventional fractionation, the application of hypofractionated PT may save patients time and money.

摘要

背景

适形分割放射治疗可能为前列腺癌带来治疗增益。我们研究了适形分割质子治疗(PT)的可行性。

材料与方法

82 例经活检证实的 T1-3N0M0 前列腺腺癌患者,且无雄激素剥夺治疗史,随机分为 5 种不同剂量方案:A 组 1,60 CGE(钴灰色等效物=质子剂量×Gy×1.1)/20 个分次/5 周;A 组 2,54 CGE/15 个分次/5 周;A 组 3,47 CGE/10 个分次/5 周;A 组 4,35 CGE/5 个分次/2.5 周;或 A 组 5,35 CGE/5 个分次/5 周。

结果

中位随访时间为 42 个月(11-52 个月)。急性 GI 和 GU 毒性≥2 级的发生率分别为 0 和 5%。晚期 GI 和 GU 毒性≥2 级的发生率分别为 16%和 7%。急性 GU 毒性最佳的是 A 组 3,晚期 GI 毒性最佳的是 A 组 2,两组均无 2 级以上毒性。4 年美国肿瘤放射治疗学会和 nadir+2ng/ml BCF 无复发生存率(BCFFS)分别为 85%和 86%。

结论

本研究中使用的前列腺腺癌适形分割 PT 是可行的,且毒性可接受。由于 BCFFS 率似乎不低于常规分割的结果,因此应用适形分割 PT 可能会为患者节省时间和金钱。

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