前列腺癌超低分次放疗与中度低分次和常规分次放疗的选择性盆腔结节照射:3项前瞻性临床试验的结果

IF 2.7 3区 医学 Q3 ONCOLOGY Clinical and Translational Radiation Oncology Pub Date : 2024-08-16 DOI:10.1016/j.ctro.2024.100843
Rachel M. Glicksman , Andrew Loblaw , Gerard Morton , Danny Vesprini , Ewa Szumacher , Hans T. Chung , William Chu , Stanley K. Liu , Chia-Lin Tseng , Melanie Davidson , Andrea Deabreu , Alexandre Mamedov , Liying Zhang , Patrick Cheung
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引用次数: 0

摘要

背景和目的前列腺癌选择性结节照射(ENI)中超低分次放疗(UHRT)的使用情况,以及与常规分次放疗(CFRT)、前列腺CFRT或中度低分次放疗(MHRT)ENI的比较,需要相关数据。材料与方法在2011-2019年间,对接受CFRT(前列腺78 Gy,39次分割;骨盆46 Gy,23次分割)、MHRT(前列腺68 Gy,25次分割;骨盆48 Gy)或UHRT(前列腺35-40 Gy,5次分割+/-前列腺内病灶50 Gy增强;骨盆25 Gy)治疗的不利的中危或高危前列腺癌患者进行了3项前瞻性临床试验。主要终点包括生化治疗失败(凤凰定义)、急性和晚期毒性反应(CTCAE v3.0/4.0):90名患者(37.5%)接受了CFRT治疗,90名患者(37.5%)接受了MHRT治疗,60名患者(25%)接受了UHRT治疗。中位随访时间为 71.6 个月(IQR 53.6-94.8)。5年后生化治疗失败的累积发生率(95 % CI)为:CFRT 11.7 %(3.5-19.8 %),MHRT 6.5 %(0.8-12.2 %),UHRT 1.8 %(0-5.2 %),不同治疗方法间无显著差异(P = 0.38)。UHRT与CFRT和MHRT相比,急性≥2级泌尿生殖系统毒性明显更严重,但急性≥3级泌尿生殖系统毒性或急性胃肠道毒性并不明显。结论前列腺癌ENI与前列腺癌CFRT/MHRT相比,前列腺癌ENI与前列腺癌UHRT的肿瘤学结果相似,急性≥2级泌尿生殖系统毒性较差,但晚期毒性无差异。采用 UHRT 技术进行 ENI 的 3 期随机试验令人期待。
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Elective pelvic nodal irradiation in the setting of ultrahypofractionated versus moderately hypofractionated and conventionally fractionated radiotherapy for prostate cancer: Outcomes from 3 prospective clinical trials

Background and purpose

Data is needed regarding the use of ultrahypofractionated radiotherapy (UHRT) in the context of prostate cancer elective nodal irradiation (ENI), and how this compares to conventionally fractionated radiotherapy (CFRT) ENI with CFRT or moderately hypofractionated radiotherapy (MHRT) to the prostate.

Materials and methods

Between 2011–2019, 3 prospective clinical trials of unfavourable intermediate or high-risk prostate cancer receiving CFRT (78 Gy in 39 fractions to prostate; 46 Gy in 23 fractions to pelvis), MHRT (68 Gy in 25 fractions to prostate; 48 Gy to pelvis), or UHRT (35–40 Gy in 5 fractions to prostate +/- boost to 50 Gy to intraprostatic lesion; 25 Gy to pelvis) were conducted. Primary endpoints included biochemical failure (Phoenix definition), and acute and late toxicities (CTCAE v3.0/4.0).

Results

Two-hundred-forty patients were enrolled: 90 (37.5 %) had CFRT, 90 (37.5 %) MHRT, and 60 (25 %) UHRT. Median follow-up time was 71.6 months (IQR 53.6–94.8). Cumulative incidence of biochemical failure (95 % CI) at 5-years was 11.7 % (3.5–19.8 %) for CFRT, 6.5 % (0.8–12.2 %) MHRT, and 1.8 % (0–5.2 %) UHRT, which was not significantly different between treatments (p = 0.38). Acute grade ≥ 2 genitourinary toxicity was significantly worse for UHRT versus CFRT and MHRT, but not for acute grade ≥ 3 genitourinary, or acute gastrointestinal toxicities. UHRT was not associated with worse late toxicities.

Conclusion

ENI with UHRT resulted in similar oncologic outcomes to CFRT ENI with prostate CFRT/MHRT, with worse acute grade ≥ 2 GU toxicity but no differences in late toxicity. Randomized phase 3 trials of ENI using UHRT techniques are much anticipated.

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来源期刊
Clinical and Translational Radiation Oncology
Clinical and Translational Radiation Oncology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.30
自引率
3.20%
发文量
114
审稿时长
40 days
期刊最新文献
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