Acute and late radiation-related toxicity after treatment of locally advanced rectal cancer with IMRT compared to 3D-CRT in the RAPIDO trial.

IF 6.4 1区 医学 Q1 ONCOLOGY
Max D Tanaka, Bengt Glimelius, Geke A P Hospers, Elma Meershoek-Klein Kranenbarg, Corrie A M Marijnen, Hein Putter, Annet G H Roodvoets, Cornelis J H van de Velde, Boudewijn van Etten, Per J Nilsson, Alice M Couwenberg
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引用次数: 0

Abstract

Purpose: Intensity-modulated radiotherapy (IMRT) aims to lower radiation-related toxicity by delivering more conformal radiotherapy compared to three-dimensional conformal radiotherapy (3D-CRT). This study investigated whether IMRT (including volumetric modulated arc therapy) resulted in less acute and late radiation-related toxicity and better treatment compliance compared to 3D-CRT in the phase III RAPIDO trial.

Methods and materials: Patients with locally advanced rectal cancer (LARC), treated with short-course radiotherapy followed by consolidation therapy (TNT arm) or chemoradiotherapy with optional postoperative chemotherapy (CRT arm) were included. IMRT was compared to 3D-CRT, stratified by treatment arm. Acute, late, and persistent toxicity endpoints included radiation-related gastrointestinal, general, genitourinary, hematological, and sexual adverse events (CTCAEv4). Toxicity endpoints were analyzed as binary outcomes (grade ≥ 1 vs. grade 0 and grade ≥ 3 vs. grade 0-2) with univariable and multivariable logistic regression analyses.

Results: For acute and late toxicity analyses, 460 and 352 patients were eligible in the TNT arm, respectively, and 441 and 321 patients in the CRT arm. IMRT was delivered in 29% of the patients. After IMRT in the TNT arm, more acute fatigue grade ≥ 1 (OR 2.71 [95%CI 1.60-4.60], p<0.001) and more acute nausea/vomiting grade ≥ 1 (OR 1.79 [95%CI 1.15-2.79], p=0.010) was observed compared to 3D-CRT. After IMRT in the CRT arm, more any late radiation-related toxicity grade ≥ 1 (OR 2.14 [95%CI 1.28-3.57], p=0.004) and more late sexual toxicity grade ≥ 1 (OR 2.31 [95%CI 1.24-4.29], p=0.008) was observed compared to 3D-CRT. No differences were found for other grade ≥ 1 toxicity endpoints, grade ≥ 3 toxicity, or treatment compliance. Persistent toxicity was rare in both groups.

Conclusions: IMRT was not associated with less radiation-related toxicity compared to 3D-CRT after TNT or CRT. In contrast, some lower grade toxicities were more frequent after IMRT, in particular fatigue during TNT. Late persistent toxicity was uncommon in both groups.

在RAPIDO试验中,与3D-CRT相比,IMRT治疗局部晚期直肠癌后的急性和晚期放射相关毒性
目的:调强放疗(IMRT)旨在通过提供比三维适形放疗(3D-CRT)更多的适形放疗来降低辐射相关毒性。本研究调查了在RAPIDO III期试验中,与3D-CRT相比,IMRT(包括体积调制电弧治疗)是否导致更少的急性和晚期辐射相关毒性以及更好的治疗依从性。方法与材料:选取局部晚期直肠癌(LARC)患者,采用短期放疗加巩固治疗(TNT组)或放化疗加术后选择性化疗(CRT组)。将IMRT与3D-CRT进行比较,按治疗组分层。急性、晚期和持续性毒性终点包括与辐射相关的胃肠道、全身、泌尿生殖系统、血液学和性不良事件(CTCAEv4)。通过单变量和多变量logistic回归分析,将毒性终点作为二元结果(≥1级vs. 0级,≥3级vs. 0-2级)进行分析。结果:对于急性和晚期毒性分析,TNT组分别有460例和352例患者符合条件,CRT组有441例和321例患者符合条件。29%的患者接受了IMRT治疗。在TNT组进行IMRT后,急性疲劳等级≥1的患者较多(OR 2.71 [95%CI 1.60-4.60])。结论:与3D-CRT相比,在TNT或CRT后,IMRT与更少的辐射相关毒性无关。相比之下,一些较低级别的毒性在IMRT后更常见,特别是TNT期间的疲劳。两组晚期持续性毒性均不常见。
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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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