Suppr超能文献

ASCENDE-RT 研究后:基于人群的分析,对于高危和不利的中危前列腺癌,联合外照射放疗和低剂量率近距离放疗的生化和生存结果。

After ASCENDE-RT: Biochemical and survival outcomes following combined external beam radiotherapy and low-dose-rate brachytherapy for high-risk and unfavourable intermediate-risk prostate cancer, a population-based analysis.

机构信息

Department of Radiation Oncology, British Columbia Cancer Agency Vancouver Centre, Vancouver, British Columbia, Canada; Department of Surgery, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Department of Radiation Oncology, British Columbia Cancer Agency Vancouver Centre, Vancouver, British Columbia, Canada; Department of Medical Physics, British Columbia Cancer Agency Vancouver Centre, Vancouver, British Columbia, Canada.

出版信息

Brachytherapy. 2022 Sep-Oct;21(5):605-616. doi: 10.1016/j.brachy.2022.05.002. Epub 2022 Jun 18.

Abstract

PURPOSE

To evaluate the outcomes of unfavorable intermediate-risk (UIR) and high-risk (HR) prostate cancer patients treated with combined external beam radiation therapy (EBRT) and low-dose-rate prostate brachytherapy (LDR-PB).

METHODS AND MATERIALS

A population-based cohort of 568 prostate cancer patients treated with combined EBRT and LDR-PB from 2010 to 2016 was analyzed. All patients received EBRT followed by LDR-PB boost. Outcomes were compared with the results for the brachytherapy arm of the ASCENDE-RT trial.

RESULTS

The median followup was 4.5 years. Sixty-nine percent (N = 391) had HR disease. Ninety-four percent of the HR and 57% of UIR were treated with androgen deprivation therapy (ADT) with a median duration of 12 months. The 5-year K-M biochemical progression-free survival (b-PFS), metastasis-free survival (MFS), and overall survival (OS) were 84 ± 2%, 90 ± 2%, and 88 ± 2%, similar to 89 ± 5%, 94 ± 4%, and 92 ± 4% for the ASCENDE-RT LDR-PB arm. The likelihood of achieving a PSA ≤0.2 ng/mL at 4 years was 88%, similar to 86% in the ASCENDE-RT LDR-PB arm. Thirty-three men (5.8%) would have been ineligible for ASCENDE-RT due to high-risk features. The 5-year K-M b-PFS, MFS and OS estimates were 86 ± 2%, 92 ± 1% and 89 ± 2% for the ASCENDE-RT eligible versus 56 ± 10% (p < 0.001), 73 ± 8% (p < 0.001), and 77 ± 9% (p = 0.098) for the ineligible patients.

CONCLUSIONS

In this population-based cohort, combining LDR-PB with pelvic EBRT (+/- ADT) achieves very favorable b-PFS that compares to the LDR-PB arm of the ASCENDE-RT, supporting the generalizability of those results. Men ineligible for ASCENDE-RT, based on prognostic features, have a much higher risk of biochemical recurrence and metastatic relapse.

摘要

目的

评估联合外部束放射治疗(EBRT)和低剂量率前列腺近距离放射治疗(LDR-PB)治疗的不利中危(UIR)和高危(HR)前列腺癌患者的治疗结果。

方法和材料

对 2010 年至 2016 年期间接受联合 EBRT 和 LDR-PB 治疗的 568 例前列腺癌患者进行了一项基于人群的队列研究。所有患者均接受 EBRT 后行 LDR-PB 加量。将结果与 ASCENDE-RT 试验中近距离放射治疗组的结果进行比较。

结果

中位随访时间为 4.5 年。69%(N=391)患者患有 HR 疾病。94%的 HR 和 57%的 UIR 患者接受了中位持续时间为 12 个月的雄激素剥夺治疗(ADT)。5 年 K-M 生化无进展生存(b-PFS)、无转移生存(MFS)和总生存(OS)分别为 84±2%、90±2%和 88±2%,与 ASCENDE-RT LDR-PB 组的 89±5%、94±4%和 92±4%相似。4 年内 PSA≤0.2ng/mL 的可能性为 88%,与 ASCENDE-RT LDR-PB 组的 86%相似。由于高危特征,33 名男性(5.8%)不符合 ASCENDE-RT 的入组条件。符合 ASCENDE-RT 标准的患者 5 年 K-M b-PFS、MFS 和 OS 估计值分别为 86±2%、92±1%和 89±2%,而不符合 ASCENDE-RT 标准的患者分别为 56±10%(p<0.001)、73±8%(p<0.001)和 77±9%(p=0.098)。

结论

在本基于人群的队列中,LDR-PB 联合盆腔 EBRT(+/-ADT)可获得非常有利的生化无进展生存,与 ASCENDE-RT 的 LDR-PB 组相当,支持这些结果的普遍性。根据预后特征,不符合 ASCENDE-RT 标准的患者生化复发和转移复发的风险要高得多。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验