Cancer Clinic, St. Olavs Hospital, Trondheim University Hospital, Norway; Department of Cancer Research and Molecular Medicine, Faculty of Medicine and Health Sciences, NTNU, Norwegian University of Science and Technology Trondheim, Norway.
Department of Cancer Research and Molecular Medicine, Faculty of Medicine and Health Sciences, NTNU, Norwegian University of Science and Technology Trondheim, Norway; Helse Møre and Romsdal, Ålesund, Norway.
Radiother Oncol. 2018 Feb;126(2):229-235. doi: 10.1016/j.radonc.2017.10.029. Epub 2018 Feb 3.
Novel cancer drugs are subject to strict scientific evaluation of safety and efficacy and usually undergo a cost effectiveness analysis before approval for use in clinical practice. For new techniques in radiotherapy (RT) such as image-guided radiotherapy (IGRT), this is often not the case. We performed a randomized controlled trial to compare daily cone beam computer tomography (CBCT) IGRT with reduced planning target volume (PTV) margins vs weekly orthogonal portal imaging with conventional PTV margins. The primary aim of the study was to investigate the effect of two different image guidance techniques on patient reported outcome (PRO) using early side effects as proxy outcome of late rectal side effects in patients receiving curative RT for prostate cancer.
This open label, phase 3 trial conducted at two RT centers in Norway enrolled men aged 18 years or older with previously untreated histologically proven intermediate or high-risk adenocarcinoma of the prostate. Patients eligible for radical RT received it after 3 months of total androgen blockage and were randomly assigned to 78 Gy in 39 fractions guided either by weekly offline orthogonal portal imaging (15 mm margins to PTV) or by daily online CBCT IGRT (7 mm margins to PTV). Based on previous results indicating that acute rectal side effects are a valid proxy outcome for late rectal side effects, the primary outcome was acute rectal toxicity at end of RT as evaluated by rectal bother scale (five of the items from PRO's QUFW94). The RIC-trial is registered with ClinicalTrials.gov, number NCT01550237.
Between October 2012 and June 2015, 257 patients were randomly assigned to weekly offline portal imaging (n = 129) or daily online CBCT IGRT (n = 128). Out of 250 evaluable patients, 96% completed PROs at baseline and 97% at end of RT. Baseline analyses demonstrated balance between groups for baseline characteristics as well as for PROs. In general, patients reported a small degree of side effects at end of RT, and there was no difference between groups for primary outcome (rectal bother scale of QUFW94 1.871 vs 1.884, p = 0.804). In addition, there were no significant differences between groups for any other gastrointestinal or urinary symptom as reported by QUFW94. Health related quality of life analyses (EORTC QLQ 30) demonstrated no differences between groups.
In radical RT for prostate cancer, daily CBCT IGRT with reduced PTV margins demonstrated no advantage with respect to patient reported side effects at end of RT as compared to weekly orthogonal offline portal imaging with standard PTV margins.
新型癌症药物的安全性和疗效需要经过严格的科学评估,通常在批准用于临床实践之前要进行成本效益分析。对于放射治疗(RT)中的新技术,如图像引导放射治疗(IGRT),通常不是这样。我们进行了一项随机对照试验,比较了每日锥形束计算机断层扫描(CBCT)IGRT 与减小计划靶区(PTV)边缘与每周正交门户成像与常规 PTV 边缘的效果。该研究的主要目的是使用早期副作用作为晚期直肠副作用的替代指标,调查两种不同的图像引导技术对接受前列腺癌根治性 RT 的患者报告结局(PRO)的影响。
这项在挪威两个 RT 中心进行的开放性、3 期试验招募了年龄在 18 岁或以上、经组织学证实患有中高危前列腺腺癌的男性。有资格接受根治性 RT 的患者在接受 3 个月的总雄激素阻断治疗后接受治疗,并随机分配至 78 Gy 共 39 次的治疗,分别由每周的离线正交门户成像(PTV 边缘为 15mm)或每日在线 CBCT IGRT(PTV 边缘为 7mm)指导。根据之前的结果表明急性直肠副作用是晚期直肠副作用的有效替代指标,主要结局是 RT 结束时直肠困扰量表(PRO 的五个项目)评估的急性直肠毒性。RIC 试验在 ClinicalTrials.gov 注册,编号为 NCT01550237。
2012 年 10 月至 2015 年 6 月期间,共有 257 名患者被随机分配至每周离线门户成像(n=129)或每日在线 CBCT IGRT(n=128)组。在 250 名可评估患者中,96%的患者在基线和 RT 结束时完成了 PRO。基线分析表明,两组在基线特征和 PRO 方面具有平衡。总的来说,患者在 RT 结束时报告了较小程度的副作用,两组之间的主要结局(QUFW94 的直肠困扰量表为 1.871 与 1.884,p=0.804)没有差异。此外,QUFW94 报告的任何其他胃肠道或尿症状两组之间也没有显著差异。健康相关生活质量分析(EORTC QLQ 30)表明两组之间没有差异。
在前列腺癌的根治性 RT 中,与每周的标准 PTV 边缘正交离线门户成像相比,使用减小 PTV 边缘的每日 CBCT IGRT 并没有显示出在 RT 结束时患者报告的副作用方面的优势。