Sinzabakira F, Brand V, Heemsbergen W D, Incrocci L
Department of Radiotherapy, Erasmus MC Cancer Institute, Dr Molewaterplein 40, 3015 GD Rotterdam, The Netherlands.
Department of Clinical Oncology, Rwanda Military Hospital, Street KK739ST, Kicukiro District, Kigali City, Rwanda.
Clin Transl Radiat Oncol. 2023 Mar 17;40:100612. doi: 10.1016/j.ctro.2023.100612. eCollection 2023 May.
Moderate hypofractionated (HF) radiotherapy is becoming the new standard in radiotherapy for prostate cancer patients. It is established as safe, but it might be associated with increased acute toxicity levels. We conducted a systematic review on moderate HF to establish acute toxicity levels and their required clinical management; late toxicity was reported as a secondary outcome.
Using PRISMA guidelines, we conducted a systematic review for studies published until June 2022. We identified 17 prospective studies, with 7796 localised prostate cancer patients, reporting acute toxicity of moderate hypofractionation (2.5-3.4 Gy/fraction). A meta-analysis was done for 10/17 studies with a control arm (standard fractionation (SF)), including evaluation of late toxicity rates. We used Cochrane bias assessment and Newcastle-Ottawa bias assessment tools for randomized controlled trials (RCTs) RCT and non-RCTs, respectively.
Pooled results showed that acute grade ≥ 2 gastro-intestinal (GI) toxicity was increased by 6.3 % (95 % CI for risk difference = 2.0 %-10.6 %) for HF vs SF. Acute grade ≥ 2 Genito-urinary (GU) and late toxicity were not significantly increased. The overall risk of bias assessment revealed a low risk in the meta-analysis of included studies. Data on management of toxicity (medication, interventions) was only reported in 2/17 studies.
HF is associated with increased acute GI symptoms, needing adequate monitoring and management. Reports on toxicity management were very limited. Pooled late GI and GU toxicity showed similar levels for SF and HF.
中等程度的低分割放疗正成为前列腺癌患者放疗的新标准。已证实其安全性,但可能与急性毒性水平增加有关。我们对中等程度低分割放疗进行了系统评价,以确定急性毒性水平及其所需的临床管理;晚期毒性作为次要结果进行报告。
我们按照PRISMA指南,对截至2022年6月发表的研究进行了系统评价。我们确定了17项前瞻性研究,涉及7796例局限性前列腺癌患者,报告了中等低分割放疗(2.5 - 3.4 Gy/分次)的急性毒性。对17项研究中的10项有对照臂(标准分割放疗(SF))的研究进行了荟萃分析,包括对晚期毒性率的评估。我们分别使用Cochrane偏倚评估工具和纽卡斯尔 - 渥太华偏倚评估工具对随机对照试验(RCT)和非RCT进行偏倚评估。
汇总结果显示,与标准分割放疗相比,低分割放疗使急性≥2级胃肠道(GI)毒性增加了6.3%(风险差异的95%置信区间 = 2.0% - 10.6%)。急性≥2级泌尿生殖系统(GU)毒性和晚期毒性没有显著增加。纳入研究的荟萃分析中总体偏倚风险评估显示风险较低。仅在17项研究中的2项报告了毒性管理(药物、干预措施)的数据。
低分割放疗与急性胃肠道症状增加有关,需要进行充分的监测和管理。关于毒性管理的报告非常有限。汇总的晚期胃肠道和泌尿生殖系统毒性显示,标准分割放疗和低分割放疗的水平相似。