介入场 SBRT 治疗结节性少复发前列腺癌的安全性和早期疗效。

IF 3.5 3区 医学 Q2 ONCOLOGY Frontiers in Oncology Pub Date : 2024-10-17 eCollection Date: 2024-01-01 DOI:10.3389/fonc.2024.1434504
Min Ji Koh, Padraig Pilkington, Min Jung Koh, Mary-Kate Lawlor, Michael Creswell, Timothy O'Connor, Alan Zwart, Malika Danner, Deepak Kumar, Simeng Suy, Michael Carrasquilla, Sean P Collins
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引用次数: 0

摘要

目的:局部前列腺癌治疗后,一部分男性会在腹盆腔结节处复发。对于放射治疗(RT)而言,最佳治疗量、分次计划和剂量仍是未解之谜。我们报告了采用介入野立体定向体放射治疗(SBRT)(IF-SBRT)治疗结节性少复发(NOR)前列腺癌患者的早期疗效:2018年1月至2023年10月期间,在乔治敦接受74个疗程IF-SBRT治疗的67名NOR前列腺癌患者符合分析条件,他们的中位年龄为75岁。NOR被定义为可在IF内安全治疗的任何疾病体积。所有患者均接受了五分频 IF-SBRT 治疗(27.5-35 Gy)。IF 治疗范围被定义为包含严重疾病的结节盆地以及紧邻的盆地。疾病进展的定义是前列腺特异性抗原(PSA)高于治疗前基线或开始第二次治疗。采用 Kaplan-Meier 法计算局部控制率和无进展生存期:前列腺特异性膜抗原(PSMA)(38%)、氟哌啶醇(50%)或核磁共振/CT(12%)检测出前列腺癌术前NOR。中位随访时间为 50 个月(1-262 个月)。痊愈前 PSA 中位数为 6.5 纳克/毫升(0.1-335)。受累结节的中位数为3个(1-16个)。1年和2年的局部控制率分别为98%和93%。1年和2年无进展生存率分别为78%和50%。20%的疗程出现急性2级胃肠道(GI)毒性:腹泻(9%)和/或恶心(14%)。两名患者(3%)出现了晚期2级恶心症状。单变量分析显示,激素敏感性(p = 0.03)、受累结节数量增加(p = 0.008)和腹腔治疗(p = 0.03)等疾病体积指标与胃肠道毒性显著相关:结论:随着 PSMA 药物的广泛应用,NORs 可能会增加。在这一人群中,局部治疗和全身治疗的最佳组合尚不清楚。IF-SBRT具有良好的毒性,是老年患者安全、方便的局部治疗选择。与患者和治疗相关的因素,如大量受累结节和/或腹腔治疗,可能与消化道毒性风险增加有关。
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Safety and early efficacy of involved-field SBRT for nodal oligo-recurrent prostate cancer.

Purpose: Following treatment for localized prostate cancer, a subset of men will develop recurrent disease in the abdominopelvic nodes. For radiation therapy (RT), the optimal treatment volume, fractionation schedule, and dose remain unanswered questions. We report early outcomes for patients treated with involved-field stereotactic body radiation therapy (SBRT) (IF-SBRT) for nodal oligo-recurrent (NOR) prostate cancer.

Methods: Between January 2018 and October 2023, 67 patients with a median age of 75 with NOR prostate cancer treated with 74 courses of IF-SBRT at Georgetown were eligible for this analysis. NOR was defined as any volume of disease that could be safely treated within an IF. All patients were treated with five-fraction IF-SBRT (27.5-35 Gy). The IF treatment volume was defined as the nodal basin containing the gross disease as well as the immediately adjacent basins. Disease progression was defined as a prostate-specific antigen (PSA) rise above the pretreatment baseline or initiation of a second treatment. Local control and progression-free survival were calculated using the Kaplan-Meier method.

Results: Detection of pre-SBRT NOR was ascertained by prostate-specific membrane antigen (PSMA) (38%), fluciclovine (50%), or MRI/CT (12%). Median follow-up was 50 months (1-262). The median pre-salvage PSA was 6.5 ng/mL (range, 0.1-335). The median number of involved nodes was 3 (range, 1-16). The local control at 1 and 2 years was 98% and 93%, respectively. The 1- and 2-year progression-free survival was 78% and 50%, respectively. Twenty percent of treatment courses were followed by acute Grade 2 gastrointestinal (GI) toxicity: diarrhea (9%) and/or nausea (14%). Two patients (3%) experienced late Grade 2 nausea. On univariate analysis, measures of disease volume such as hormone sensitivity (p = 0.03), increasing involved node number (p = 0.008), and abdominal treatment (p = 0.03) were significantly associated with GI toxicity.

Conclusions: With the widespread adoption of PSMA agents, NORs are likely to increase. The optimal combination of local and systemic therapy in this population is unknown. With a favorable toxicity profile, IF-SBRT represents a safe and convenient local therapy treatment option for an elderly patient population. Patient- and treatment-related factors such as a large number of involved nodes and/or abdominal treatment may be associated with an increased risk of GI toxicity.

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来源期刊
Frontiers in Oncology
Frontiers in Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
6.20
自引率
10.60%
发文量
6641
审稿时长
14 weeks
期刊介绍: Cancer Imaging and Diagnosis is dedicated to the publication of results from clinical and research studies applied to cancer diagnosis and treatment. The section aims to publish studies from the entire field of cancer imaging: results from routine use of clinical imaging in both radiology and nuclear medicine, results from clinical trials, experimental molecular imaging in humans and small animals, research on new contrast agents in CT, MRI, ultrasound, publication of new technical applications and processing algorithms to improve the standardization of quantitative imaging and image guided interventions for the diagnosis and treatment of cancer.
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