Ferro Marica, Ferro Milena, Macchia Gabriella, Cilla Savino, Buwenge Milly, Re Alessia, Romano Carmela, Boccardi Mariangela, Picardi Vincenzo, Cammelli Silvia, Cucci Eleonora, Mignogna Samantha, Di Lullo Liberato, Valentini Vincenzo, Morganti Alessio Giuseppe, Deodato Francesco
Radiation Oncology Unit, Gemelli Molise Hospital - Università Cattolica del Sacro Cuore, Campobasso, Italy.
Medical Physics Unit, Gemelli Molise Hospital - Università Cattolica del Sacro Cuore, Campobasso, Italy.
Front Oncol. 2021 Feb 22;10:626400. doi: 10.3389/fonc.2020.626400. eCollection 2020.
Glioblastoma Multiforme (GBM) is the most common primary brain cancer and one of the most lethal tumors. Theoretically, modern radiotherapy (RT) techniques allow dose-escalation due to the reduced irradiation of healthy tissues. This study aimed to define the adjuvant maximum tolerated dose (MTD) using volumetric modulated arc RT with simultaneous integrated boost (VMAT-SIB) plus standard dose temozolomide (TMZ) in GBM.
A Phase I clinical trial was performed in operated GBM patients using VMAT-SIB technique with progressively increased total dose. RT was delivered in 25 fractions (5 weeks) to two planning target volumes (PTVs) defined by adding a 5-mm margin to the clinical target volumes (CTVs). The CTV was the tumor bed plus the MRI enhancing residual lesion with 10-mm margin. The CTV was the CTV plus 20-mm margin. Only PTV dose was escalated (planned dose levels: 72.5, 75, 77.5, 80, 82.5, 85 Gy), while PTV dose remained unchanged (45 Gy/1.8 Gy). Concurrent and sequential TMZ was prescribed according to the EORTC/NCIC protocol. Dose-limiting toxicities (DLTs) were defined as any G ≥ 3 non-hematological acute toxicity or any G ≥ 4 acute hematological toxicities (RTOG scale) or any G ≥ 2 late toxicities (RTOG-EORTC scale).
Thirty-seven patients (M/F: 21/16; median age: 59 years; median follow-up: 12 months) were enrolled and treated as follows: 6 patients (72.5 Gy), 10 patients (75 Gy), 10 patients (77.5 Gy), 9 patients (80 Gy), 2 patients (82.5 Gy), and 0 patients (85 Gy). Eleven patients (29.7%) had G1-2 acute neurological toxicity, while 3 patients (8.1%) showed G ≥ 3 acute neurological toxicities at 77.5 Gy, 80 Gy, and 82.5 Gy levels, respectively. Since two DLTs (G3 neurological: 1 patient and G5 hematological toxicity: 1 patient) were observed at 82.5 Gy level, the trial was closed and the 80 Gy dose-level was defined as the MTD. Two asymptomatic histologically proven radionecrosis were recorded.
According to the results of this Phase I trial, 80 Gy in 25 fractions accelerated hypofractionated RT is the MTD using VMAT-SIB plus standard dose TMZ in resected GBM.
多形性胶质母细胞瘤(GBM)是最常见的原发性脑癌,也是最致命的肿瘤之一。从理论上讲,现代放疗(RT)技术由于减少了对健康组织的照射,从而允许增加剂量。本研究旨在确定在GBM中使用容积调强弧形放疗联合同步整合加量(VMAT-SIB)及标准剂量替莫唑胺(TMZ)时的辅助最大耐受剂量(MTD)。
对接受手术的GBM患者进行了一项I期临床试验,采用VMAT-SIB技术,总剂量逐步增加。放疗分25次(5周)给予两个计划靶区(PTV),PTV是在临床靶区(CTV)周围添加5mm边界定义的。CTV是肿瘤床加上MRI增强的残留病灶,并带有10mm边界。PTV是CTV加上20mm边界。仅增加PTV剂量(计划剂量水平:72.5、75、77.5、80、82.5、85Gy),而PTV剂量保持不变(45Gy/1.8Gy)。根据欧洲癌症研究与治疗组织/加拿大国家癌症研究所(EORTC/NCIC)方案给予同步和序贯TMZ。剂量限制毒性(DLT)定义为任何≥3级的非血液学急性毒性或任何≥4级的急性血液学毒性(RTOG分级)或任何≥2级的晚期毒性(RTOG-EORTC分级)。
37例患者(男/女:21/16;中位年龄:59岁;中位随访时间:12个月)入组并接受如下治疗:6例(72.5Gy)、10例(75Gy)、10例(77.5Gy)、9例(80Gy)、2例(82.5Gy)和0例(85Gy)。11例患者(29.7%)有1-2级急性神经毒性,而分别有3例患者(8.1%)在77.5Gy、80Gy和82.5Gy剂量水平出现≥3级急性神经毒性。由于在82.5Gy剂量水平观察到2例DLT(1例3级神经毒性和1例5级血液学毒性),试验终止,80Gy剂量水平被定义为MTD。记录到2例无症状的经组织学证实的放射性坏死。
根据这项I期试验的结果,在切除的GBM中,25次分割、总剂量80Gy的加速超分割放疗是使用VMAT-SIB联合标准剂量TMZ时的MTD。