Hoegen-Saßmannshausen Philipp, Renkamp C Katharina, Lau Hoi Hin, Neugebauer David, Niebuhr Nina, Buchele Carolin, Schlüter Fabian, Sandrini Elisabetta, Hoeltgen Line, Weykamp Fabian, Regnery Sebastian, Liermann Jakob, Meixner Eva, Zhang Kevin, Sedlaczek Oliver, Schlemmer Heinz-Peter, König Laila, Debus Jürgen, Klüter Sebastian, Hörner-Rieber Juliane
Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany.
Heidelberg Institute of Radiation Oncology (HIRO), Heidelberg, Germany.
Clin Transl Radiat Oncol. 2025 Feb 28;52:100941. doi: 10.1016/j.ctro.2025.100941. eCollection 2025 May.
PURPOSE/OBJECTIVE: To compare online MR-guided SBRT (MRgRT) of liver metastases with state-of-the-art ITV-based SBRT (ITV-SBRT) and assess which patients benefit most from MRgRT.
In a prospective randomized trial (MAESTRO study, NCT05027711), patients were randomized to either gated and online adaptive MRgRT or ITV-SBRT if a biologically effective dose (BED) of 100 Gy was feasible with ITV-SBRT. Otherwise, patients were treated with MRgRT. In this subgroup analysis of 20 patients, a dosimetric comparison of MRgRT and ITV-SBRT plans was performed. Tumor control and normal tissue complication probabilities were calculated.
In 40 % of all patients, MRgRT enabled SBRT with less fractions and/or higher prescription BED. Almost all target volume metrics were improved with MRgRT. MRgRT PTV D95% was significantly higher in the overall cohort (91.0 ± 22.9 Gy vs. 79.5 ± 27.2 Gy, p = 0.001), in uncritical (111.3 ± 6.2 Gy vs. 104.7 ± 4.1 Gy, p = 0.022) and in critical cases with limited healthy liver volume or nearby gastrointestinal organs at risk (74.1 ± 16.9 Gy vs. 58.5 ± 18.5 Gy, p = 0.041). Target volume V100% was also superior with MRgRT. Calculated 2-year tumor control probability was significantly superior with MRgRT overall (73.0 ± 6.2 % vs. 69.7 ± 7.9 %, p = 0.002), in uncritical cases (78.3 ± 1.4 % vs. 76.8 ± 1.0 %, p = 0.022) and in critical cases (68.5 ± 4.8 % vs. 63.8 ± 5.8 %, p = 0.041), without elevated normal tissue complication probability.
Dosimetrically, gated MRgRT was beneficial for virtually all the hepatic metastases analyzed in this study. Patients with metastases located critically near gastrointestinal OAR or with limited healthy liver volume should be allocated to centers providing MRgRT.
目的/目标:比较肝脏转移瘤的在线磁共振引导下立体定向放疗(MRgRT)与基于先进的内部靶区(ITV)的立体定向放疗(ITV-SBRT),并评估哪些患者从MRgRT中获益最大。
在一项前瞻性随机试验(MAESTRO研究,NCT05027711)中,如果ITV-SBRT可行的生物等效剂量(BED)为100 Gy,则将患者随机分为门控和在线自适应MRgRT组或ITV-SBRT组。否则,患者接受MRgRT治疗。在对20例患者的该亚组分析中,对MRgRT和ITV-SBRT计划进行了剂量学比较。计算肿瘤控制率和正常组织并发症概率。
在所有患者中,40%的患者通过MRgRT进行立体定向放疗时所需分次更少和/或处方BED更高。几乎所有靶区体积指标在MRgRT下均得到改善。在整个队列中,MRgRT计划的计划靶区(PTV)D95%显著更高(91.0±22.9 Gy对79.5±27.2 Gy,p = 0.001),在非关键病例中(111.3±6.2 Gy对104.7±4.1 Gy,p = 0.022)以及在健康肝脏体积有限或附近有胃肠道器官受照射风险的关键病例中(74.1±16.9 Gy对58.5±18.5 Gy,p = 0.041)。靶区体积V100%在MRgRT下也更优。总体计算得出的2年肿瘤控制率在MRgRT下显著更高(73.0±±6.2%对69.7±7.9%,p = 0.002),在非关键病例中(78.3±1.4%对76.8±1.0%,p = 0.022)以及在关键病例中(68.5±4.8%对63.8±5.8%,p = 0.041),且正常组织并发症概率未升高。
从剂量学角度看,门控MRgRT对本研究中分析的几乎所有肝转移瘤均有益。转移瘤位置紧邻胃肠道危及器官或健康肝脏体积有限的患者应分配至提供MRgRT的中心。