Jaspan T, Morgan P S, Warmuth-Metz M, Sanchez Aliaga E, Warren D, Calmon R, Grill J, Hargrave D, Garcia J, Zahlmann G
From Nottingham University Hospitals National Health Service Trust (T.J., P.S.M.), Nottingham, UK
From Nottingham University Hospitals National Health Service Trust (T.J., P.S.M.), Nottingham, UK.
AJNR Am J Neuroradiol. 2016 Sep;37(9):1581-7. doi: 10.3174/ajnr.A4782. Epub 2016 Apr 28.
Determination of tumor response to treatment in neuro-oncology is challenging, particularly when antiangiogenic agents are considered. Nontumoral factors (eg, blood-brain barrier disruption, edema, and necrosis) can alter contrast enhancement independent of true tumor response/progression. Furthermore, gliomas are often infiltrative, with nonenhancing components. In adults, the Response Assessment in Neuro-Oncology (RANO) criteria attempted to address these issues. No such guidelines exist yet for children. The ongoing randomized phase II trial, A Study of Avastin (bevacizumab) in Combination With Temolozomide (TMZ) and Radiotherapy in Paediatric and Adolescent Patients With High-Grade Glioma (HERBY), will establish the efficacy and safety of the antiangiogenic agent bevacizumab for the first-line treatment of newly diagnosed high-grade glioma in children (n = 121 patients, enrollment complete). The primary end point is event-free survival (tumor progression/recurrence by central review, second primary malignancy, or death). Determination of progression or response is based on predefined clinical and radiographic criteria, modeled on the RANO criteria and supported by expert pseudoprogression review and the use of standardized imaging protocols. The HERBY trial will also compare conventional MR imaging (T1-weighted and T2/fluid-attenuated inversion recovery sequences) with conventional MR imaging plus diffusion/perfusion imaging for response assessment. It is anticipated that HERBY will provide new insights into antiangiogenic-treated pediatric brain tumors. HERBY will also investigate the practicality of obtaining adequate quality diffusion/perfusion scans in a trial setting, and the feasibility of implementing standard imaging protocols across multiple sites. To date, 61/73 (83.6%) patients with available data have completed diffusion-weighted imaging (uptake of other nonconventional techniques has been limited). Harmonization of imaging protocols and techniques may improve the robustness of pediatric neuro-oncology studies and aid future trial comparability.
在神经肿瘤学中,确定肿瘤对治疗的反应具有挑战性,尤其是在考虑使用抗血管生成药物时。非肿瘤因素(如血脑屏障破坏、水肿和坏死)可独立于真正的肿瘤反应/进展而改变对比增强。此外,胶质瘤通常具有浸润性,包含无强化成分。在成人中,神经肿瘤学反应评估(RANO)标准试图解决这些问题。目前尚无针对儿童的此类指南。正在进行的随机II期试验“阿瓦斯汀(贝伐单抗)联合替莫唑胺(TMZ)及放疗治疗儿童和青少年高级别胶质瘤的研究(HERBY)”,将确定抗血管生成药物贝伐单抗用于儿童新诊断高级别胶质瘤一线治疗的疗效和安全性(n = 121例患者,已完成入组)。主要终点是无事件生存期(经中心审查的肿瘤进展/复发、第二原发性恶性肿瘤或死亡)。进展或反应的确定基于预定义的临床和影像学标准,以RANO标准为模型,并得到专家伪进展审查和标准化成像方案使用的支持。HERBY试验还将比较传统磁共振成像(T1加权和T2/液体衰减反转恢复序列)与传统磁共振成像加弥散/灌注成像用于反应评估。预计HERBY将为抗血管生成治疗的儿童脑肿瘤提供新的见解。HERBY还将研究在试验环境中获得足够质量的弥散/灌注扫描的实用性,以及在多个地点实施标准成像方案的可行性。迄今为止,61/73(83.6%)有可用数据的患者已完成弥散加权成像(其他非传统技术的应用有限)。成像方案和技术的统一可能会提高儿童神经肿瘤学研究的稳健性,并有助于未来试验的可比性。