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1000例患者中1.5T磁共振引导下每日适应性放疗的临床可行性与安全性:早期采用中心的真实世界大型经验

The Clinical Feasibility and Safety of 1.5 T MR-Guided Daily Adapted Radiotherapy in 1000 Patients: A Real-World Large Experience of an Early-Adopter Center.

作者信息

De-Colle Chiara, Rigo Michele, Allegra Andrea Gaetano, Nicosia Luca, Giaj-Levra Niccolò, Pastorello Edoardo, Ricchetti Francesco, Orsatti Carolina, Romei Andrea, Bianchi Nicola, Borgese Riccardo Filippo, De Simone Antonio, Gurrera Davide, Naccarato Stefania, Sicignano Gianluisa, Ruggieri Ruggero, Alongi Filippo

机构信息

Department of Advanced Radiation Oncology, Cancer Care Center, IRCCS Sacro Cuore Don Calabria Hospital, 37024 Negrar di Valpolicella, VR, Italy.

University of Brescia, 25121 Brescia, BR, Italy.

出版信息

Cancers (Basel). 2025 Jun 17;17(12):2012. doi: 10.3390/cancers17122012.

Abstract

PURPOSE/OBJECTIVE: The clinical implementation of MR-guided radiotherapy on MR-linacs (MRL) hasrapidly increased in recent years. The advantages represented by the MR-based daily online plan adaptation and real-time monitoring have been exploited for different tumor sites. Nevertheless, some concerns remain, mainly related to the longer treatment time and limited patient eligibility. We report here the experience of our center, where a 1.5T MRL was clinically implemented in 2019 and, since then, more than 1200 patients have been treated.

MATERIAL AND METHODS

The first 1000 patients treated at the MRL in our department were selected. Technical information such as treatment time and adaptive technic have been prospectively recorded, while toxicity data were retrospectively collected.

RESULTS

Between October 2019 and June 2024, 1000 patients for a total of 1061 treatment courses were included. Prostate and prostate bed were irradiated in 57.1% and 10.2% of the cases, respectively, including regional pelvic lymphnodes in 4.7%. Other frequent treated sites were lymph node metastases, pancreas and liver. The most frequent prescribed doses were 36.25 Gy (31%), 35 Gy (28.3%) and 30 Gy (9.4%) in five fractions. On a total of 9076 administered fractions, 80.8% were performed with adapt-to-shape and 19.2% with adapt-to-position method. The mean in-room time was 38 min (range, 18-103), with 74.4% of patients completing the session within 40 min. Acute grade (G) 3 toxicity was recorded in 1.6% of the cases, while, on a total of 858 patients available for late toxicity, G3 was recorded in 0.3% of the cases, with no >G3.

CONCLUSIONS

Our real-world experience of an early-adopter center confirms that MRL treatments are feasible for different tumor entities in several anatomical sites. We showed that most of the patients could be treated within 40 min and showed low toxicity rates. Protocols for dose escalation and margin reduction, by adopting new comprehensive motion monitoring strategies, are under development.

摘要

目的/目标:近年来,磁共振引导放疗在磁共振直线加速器(MRL)上的临床应用迅速增加。基于磁共振的每日在线计划调整和实时监测所带来的优势已被应用于不同肿瘤部位。然而,仍存在一些担忧,主要与治疗时间较长和患者入选标准有限有关。我们在此报告我们中心的经验,该中心于2019年临床应用了一台1.5T的MRL,自那时起,已治疗了1200多名患者。

材料与方法

选取了我们科室在MRL上治疗的前1000例患者。前瞻性记录了治疗时间和自适应技术等技术信息,同时回顾性收集了毒性数据。

结果

在2019年10月至2024年6月期间,共纳入1000例患者,进行了1061个疗程的治疗。前列腺和前列腺床的照射分别占病例的57.1%和10.2%,其中包括区域盆腔淋巴结照射的占4.7%。其他常见的治疗部位是淋巴结转移灶、胰腺和肝脏。最常用的处方剂量是36.25 Gy(31%)、35 Gy(28.3%)和30 Gy(9.4%),分五次照射。在总共9076次给药照射中,80.8%采用形状适配法进行,19.2%采用位置适配法进行。平均室内时间为38分钟(范围为18 - 103分钟),74.4%的患者在40分钟内完成治疗。1.6%的病例记录有急性3级(G)毒性,而在总共858例可进行晚期毒性评估的患者中,0.3%的病例记录有G3毒性,无大于G3级的毒性。

结论

我们作为早期采用中心的真实世界经验证实,MRL治疗对于多个解剖部位的不同肿瘤实体是可行的。我们表明,大多数患者可以在40分钟内完成治疗,且毒性率较低。目前正在制定通过采用新的综合运动监测策略来提高剂量和缩小 margins 的方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f65/12191406/6c439630072a/cancers-17-02012-g001.jpg

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