首页> 外文期刊>AJNR. American journal of neuroradiology >Response Assessment in Pediatric Neuro-Oncology: Implementation and Expansion of the RANO Criteria in a Randomized Phase H Trial of Pediatric Patients with Newly Diagnosed High-Grade Gliomas
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Response Assessment in Pediatric Neuro-Oncology: Implementation and Expansion of the RANO Criteria in a Randomized Phase H Trial of Pediatric Patients with Newly Diagnosed High-Grade Gliomas

机译:儿科神经肿瘤学中的反应评估:在新诊断为高级别胶质瘤的小儿患者的随机H期试验中,RANO标准的实施和扩展

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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 (Ti-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.
机译:在神经肿瘤学中确定肿瘤对治疗的反应具有挑战性,特别是在考虑使用抗血管生成剂时。非肿瘤因素(例如血脑屏障破坏,水肿和坏死)可以改变造影剂的增强,而与真实的肿瘤反应/进展无关。此外,神经胶质瘤通常是浸润性的,具有不增强的成分。在成人中,神经肿瘤反应评估(RANO)标准试图解决这些问题。尚无针对儿童的此类指南。正在进行的随机化II期临床试验,阿瓦斯汀(贝伐单抗)与替莫罗米特(TMZ)联合放疗对小儿和青少年重度脑胶质瘤患者(HERBY)的研究,将确定抗血管生成药贝伐单抗对糖尿病的疗效和安全性儿童新诊断的高级别神经胶质瘤的一线治疗(n = 121例患者,入组完成)。主要终点是无事件生存(通过中心评估得出的肿瘤进展/复发,第二原发恶性肿瘤或死亡)。进展或反应的确定基于预定义的临床和放射学标准,以RANO标准为模型,并得到专家的伪进展审查和标准成像协议的支持。 HERBY试验还将比较常规MR成像(Ti加权和T2 /流体衰减的反转恢复序列)与常规MR成像加扩散/灌注成像以进行反应评估。预计HERBY将为抗血管生成治疗的小儿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扩散/灌注扫描的实用性,以及在多个站点实施标准成像协议的可行性。迄今为止,已有数据的61/73(83.6%)患者已完成弥散加权成像(其他非常规技术的使用受到限制)。成像协议和技术的统一可以提高小儿神经肿瘤学研究的鲁棒性,并有助于将来的试验可比性。

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