IMRT-VMAT治疗局部晚期直肠腺癌:一项基于Rapido试验的全新辅助放疗的多中心观察性前瞻性研究

G. Lazzari, I. Benevento, A. Montagna, B. d'Andrea, G. Castaldo, A. Bianculli, R. Tucciariello, G. Calice, G. Storto, Alessia Giordano, A. Solazzo
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引用次数: 0

摘要

背景:III期多中心随机RAPIDO试验(直肠癌和术前诱导治疗后专用手术)显示了全新辅助治疗(TNT)与短程放疗(RT)的优势。然而,在5.6年的中位随访中,TNT组的局部控制数据尚未得到证实,因为实验(EXP)组的患者接受3D-CRT的频率更高(p=0.029)。这项多中心观察性前瞻性研究的主要终点是评估RAPIDO试验方案在所有入组患者中使用VMAT和IMRT治疗的现实生活安全性和有效性。此外,还将提供FDG-PET和MRI图像与癌症表型(K-ras和EGFR状态)的预测特征进行比较,并研究肿瘤微环境对短期RT的反应。方法:纳入RAPIDO试验中定义的接受TNT治疗的局部晚期直肠癌患者,前瞻性纳入本研究。MRI和FDG-PET将对疾病进行分期和再分期。用免疫表型、可溶性PDL1和EVCs对肿瘤微环境变化进行评估。对于样本量计算,使用OR 0.5,将入组100例患者,为期两年。对OS、DFS和预测因子进行局部控制,采用Kaplan -模型和比例Cox法。结论:本研究的结果将有助于通过放射组学、代谢组学和免疫学特征来预测VMAT和IMRT治疗短期TNT的安全性和有效性。试验登记:区域委员会第50/2022号;圣卡洛医院,波坦察,意大利。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IMRT-VMAT in Locally Advanced Rectal Adenocarcinoma: An Observational Multicenter Prospectic Study on Total Neoadiuvant Radiotherapy According Rapido Trial
Background: The phase III multicenter randomized RAPIDO trial (Rectal Cancer And Preoperative Induction therapy followed by Dedicated Operation) has shown the advantege of Total Neoadjuvant treatment (TNT) with short course radiotherapy (RT). However, data on local control have not been confirmed at 5.6 years median follow-up in favor of the TNT arm because patients from the experimental (EXP) group received more often 3D-CRT (p=0.029). The primary end-point of this multicentric observational prospectic study is to assess the real life safety and efficacy of RAPIDO trial protocol using VMAT and IMRT treatment in all enrolled patients. Moreover FDG-PET and MRI images for predictive features compared with cancer phenotype (status of K-ras and EGFR) and study on tumor microenviroment response to short course RT will be also provided. Methods: Locally advanced rectal cancer patients undergoing TNT as defined in RAPIDO trial will be enrolled and prospectively included in this study. MRI and FDG-PET will be performed to staging and restaging the disease. The tumor microenviroment changes assessment with immunophenotype and soluble PDL1 and on EVCs will be done. For sample size calculation, using OR 0.5, 100 patients will be enrolled into two years. Kaplan -model and proportional Cox method will be adopoted for OS, DFS and predictive factors for local control. Conclusions: The results of this study will be useful to assess prospectively the safety and effectiveness of VMAT and IMRT in short course TNT assuming predictive factors for response through radiomics, metabolomics and immunological features. Trial Registration: COMITATO ETICO UNICO REGIONALE (CEUR) N.50/2022; San Carlo Hospital, Potenza, Italy.
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