使用非适应性磁共振引导放疗的前列腺 SBRT 临床疗效。

IF 2.5 4区 医学 Q3 ONCOLOGY
Maria L Sandoval, Anupam Rishi, Kujtim Latifi, G Daniel Grass, Javier Torres-Roca, Stephen A Rosenberg, Kosj Yamoah, Peter A S Johnstone
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引用次数: 0

摘要

目的:立体定向体放射治疗(SBRT)被广泛应用于前列腺癌的局部治疗,采用磁共振引导放疗的优点是边缘更紧密,能更好地保护危险器官。在此,我们对本机构使用非适应性磁共振引导 SBRT(MRgSBRT)治疗局部前列腺癌的疗效和所需时间进行了评估:从 2019 年 9 月至 2021 年 11 月,我们对连续接受前列腺 MRgSBRT 治疗的 80 例患者进行了回顾性审查。患者包括低危(LR)(5%)、中危(FIR)(40%)、中危(UIR)(49%)和高危(HR)(6%)。32%的患者采用了短期雄激素剥夺疗法。靶区包括前列腺和精囊近端,边缘各向同性为3毫米。治疗剂量为36.25 Gy,每隔一天治疗5次,同时保留尿道。18%的患者使用了水凝胶垫片。直列加速器上的时间记录为光束照射时间(BOT)加上总治疗时间(TTT),包括门控时间。分析结果包括PSA反应、由美国泌尿协会(AUA)问卷评分的患者报告结果以及CTCAE v5规定的毒性。 采用一般线性回归模型分析影响纵向随访中PSA和AUA的因素,采用卡方检验评估影响毒性的因素:中位随访时间为19.3个月(3.8 - 36.6)。中位 BOT 为 4.6 分钟(2.6 - 7.2),中位 TTT 为 11 分钟(7.6 - 15.8)。治疗前与治疗后的中位 PSA 分别为 6.36(2.20 - 19.6)vs 0.85(0.19 - 3.6)(P < 0.001)。按风险类别对患者进行分层后,PSA下降幅度有明显差异,LR/FIR组与UIF/HR组更有利(P = 0.019)。4例(5%)患者出现生化失败(BCF),中位生化失败时间为20.4个月(7.9 - 34.5)。中位无生化失败生存期(BCFFS)未达标,2年和4年的BCFFS分别为97.1%和72.1%。LR/FIR患者的2年和4年无生化失败生存率为100%,而UIF/HR患者的2年和4年无生化失败生存率分别为95%和41%(P = 0.05)。治疗前的平均 AUA 为 7.3(1 - 25),首次随访时为 11.3(1 - 26);但随着时间的推移,AUA 恢复到基线水平。尿道 Dmax ≥35 Gy 的患者在所有随访中的 AUA 评分均呈下降趋势(P = 0.07)。41名(51%)患者在1个月的随访中报告了1-2级泌尿生殖系统毒性。1名患者出现了3级毒性(直肠炎)。使用水凝胶垫片后,任何级别的直肠毒性均未减少(3 vs 6,P = 0.2)。未观察到≥4级毒性:结论:MRgSBRT具有适应治疗的潜力,但这是以增加资源利用率为代价的。我们在前列腺非适应性 MRgSBRT 方面的经验表明,该疗法治疗时间短、疗效好、PSA 控制良好且毒性低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Outcomes of Prostate SBRT Using Non-adaptive MR-Guided Radiotherapy.

Objectives: Stereotactic body radiotherapy (SBRT) is widely used for localized prostate cancer and implementation of MR-guided radiotherapy has the advantage of tighter margins and improved sparing of organs at risk. Here we evaluate outcomes and time required to treat using non-adaptive MR-guided SBRT (MRgSBRT) for localized prostate cancer at our institution.

Methods: From 9/2019 to 11/2021 we conducted a retrospective review of 80 consecutive patients who were treated with MRgSBRT to the prostate. Patients included low (LR) (5%), favorable intermediate (FIR) (40%), unfavorable intermediate (UIR) (49%), and high risk (HR) (6%). Short-term androgen deprivation therapy was used in 32% of patients. Target volumes included prostate gland and proximal seminal vesicles with an isotropic 3 mm margin. Treatment was prescribed to 36.25 Gy in 5 fractions every other day with urethral sparing. Hydrogel spacer was used in 18% of patients. Time on the linac was recorded as beam on time (BOT) plus total treatment time (TTT) including gating. Analyzed outcomes included PSA response and patient reported outcomes scored by the American Urological Association (AUA) questionnaire and toxicity per CTCAE v5. General linear regression model was used to analyze factors affecting PSA and AUA in longitudinal follow up, and chi-square test was used to assess factors affecting toxicity.

Results: Median follow up was 19.3 months (3.8 - 36.6). Median BOT was 4.6 min (2.6 - 7.2) with a median TTT of 11 min (7.6 - 15.8). Pre-treatment vs post-RT median PSA was 6.36 (2.20 - 19.6) vs 0.85 (0.19 - 3.6), respectively (P < 0.001). PSA decrease differed significantly when patients were stratified by risk category, favoring LR/FIR vs UIF/HR group (P = 0.019). Four (5%) patients experienced a biochemical failure (BCF), with a median time to BCF of 20.4 months (7.9 - 34.5). Median biochemical failure free survival (BCFFS) was not reached, with 2-yr and 4-yr BCFFS of 97.1% and 72.1%, respectively. Patients with LR/FIR disease had 100% 2-yr and 4-yr BCFFS, whereas patients with UIF/HR had 95% and 41% 2-yr and 4-yr BCFFS (P = 0.05). Mean pre-treatment AUA was 7.3 (1 - 25) vs 11.3 (1 - 26) at first follow-up; however, AUA normalized to baseline over time. Urethral Dmax ≥35 Gy trended to lower AUA score at all follow-ups (P = 0.07). Forty-one (51%) patients reported grade 1-2 genitourinary toxicities at the 1 month follow up. Grade 3 toxicity (proctitis) was noted in 1 patient. There was no decrease in any grade rectal toxicity with use of hydrogel spacer (3 vs 6, P = 0.2). No grade ≥4 toxicities was observed.

Conclusions: MRgSBRT has the potential for treatment adaptation but this comes at the cost of increased resource utilization. Our experience with non-adaptive MRgSBRT of the prostate highlights its short treatment times as well as efficacy with good PSA control and low toxicity profile.

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来源期刊
Cancer Control
Cancer Control ONCOLOGY-
CiteScore
3.80
自引率
0.00%
发文量
148
审稿时长
>12 weeks
期刊介绍: Cancer Control is a JCR-ranked, peer-reviewed open access journal whose mission is to advance the prevention, detection, diagnosis, treatment, and palliative care of cancer by enabling researchers, doctors, policymakers, and other healthcare professionals to freely share research along the cancer control continuum. Our vision is a world where gold-standard cancer care is the norm, not the exception.
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