Stereotactic ablative radiotherapy extends time to subsequent systemic therapy in pediatric cancer patients with recurrent or metastatic disease

IF 2
EJC paediatric oncology Pub Date : 2026-06-01 Epub Date: 2026-05-26 DOI:10.1016/j.ejcped.2026.100526
Sean P. Hassan , Nisha Shariff , Xuan Li , Yuan Zhong , Alejandro Shiri Moreno , Dana M. Keilty , David C. Hodgson , Paul C. Nathan , Furqan Shaikh , Anita Villani , David Malkin , Avram Denburg , Kriti Kumar , Derek S. Tsang
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引用次数: 0

Abstract

Background and Aims

Stereotactic ablative radiotherapy (SAbR) has been used in the adult population for decades, providing local control (LC) and, in some cases, overall survival (OS) advantage. It can also extend the time to subsequent systemic therapy, reducing side effect burden and improving quality of life. This retrospective study aimed to evaluate the effectiveness of SAbR in prolonging time to subsequent systemic therapy in children.

Methods

We performed a single-institution retrospective analysis of children who underwent extracranial SAbR over 2 – 5 fractions (dose per fraction > 5 Gray [Gy]) for recurrent or progressive cancer between 2009 and 2024. The primary endpoint was time from SAbR to next use of systemic therapy. Secondary endpoints included LC and OS, as well as the impact of biological effective dose (BED) and equivalent dose in 2-Gy fractions (EQD2) thereon.

Results

Thirty-five pediatric patients with cancer had 97 lesions that received at least one course of SAbR meeting minimum dose criteria (BED10 ≥30 Gy). The cumulative incidence of any systemic therapy change at 12 months was 0.58 (95% CI 0.47–0.68). The cumulative incidence of IV systemic therapy change at 12 months was 0.36 (95% CI 0.26–0.47), with a median time to IV systemic therapy change of 11.9 months. Risk of local progression was associated with non-sarcoma histology compared with soft tissue sarcoma (Hazard Ratio [HR] 4.19; 95% Confidence Interval [CI] 1.25–14.06; p = 0.021). Median OS from first SAbR was 12.8 months (95% CI 7.82–26.20). There was no statistically significant association of LC with BED or EQD2.

Conclusions

In this single-institution case series, SAbR was associated with a delay to subsequent IV systemic therapy change in pediatric cancer patients and may serve as a means to manage disease progression while minimizing burden of therapy. Prospective studies are needed to confirm these findings.
立体定向消融放疗延长了儿童癌症复发或转移患者后续全身治疗的时间
背景和目的立体定向消融放疗(SAbR)已经在成人人群中使用了几十年,提供局部控制(LC),在某些情况下,提供总生存(OS)优势。它还可以延长后续全身治疗的时间,减轻副作用负担,提高生活质量。本回顾性研究旨在评估SAbR在延长儿童后续全身治疗时间方面的有效性。方法:我们对2009年至2024年间因复发或进展性癌症接受颅外SAbR治疗的儿童进行了单机构回顾性分析(剂量/分数>; 5 Gray [Gy])。主要终点是从SAbR到下一次全身治疗的时间。次要终点包括LC和OS,以及生物有效剂量(BED)和2 gy组分等效剂量(EQD2)对其的影响。结果35例儿童癌症患者有97个病灶接受了至少一个疗程的SAbR治疗,符合最低剂量标准(BED10 ≥30 Gy)。12个月时任何系统性治疗改变的累积发生率为0.58 (95% CI 0.47-0.68)。12个月静脉全身治疗改变的累积发生率为0.36 (95% CI 0.26-0.47),静脉全身治疗改变的中位时间为11.9个月。与软组织肉瘤相比,局部进展的风险与非肉瘤组织学相关(风险比[HR] 4.19; 95%可信区间[CI] 1.25-14.06; p = 0.021)。首次SAbR的中位OS为12.8个月(95% CI 7.82-26.20)。LC与BED或EQD2的相关性无统计学意义。结论:在这个单机构的病例系列中,SAbR与儿童癌症患者后续静脉系统治疗改变的延迟有关,可以作为控制疾病进展的一种手段,同时减少治疗负担。需要前瞻性研究来证实这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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