Rumley Christopher N, Lee Mark T, Holloway Lois, Rai Robba, Min Myo, Forstner Dion, Fowler Allan, Liney Gary
Department of Radiation Oncology, Cancer Therapy Centre, Liverpool Hospital, Liverpool, NSW, Australia.
South Western Clinical School, School of Medicine, University of New South Wales, Sydney, NSW, Australia.
BMC Cancer. 2017 Jul 10;17(1):475. doi: 10.1186/s12885-017-3448-5.
Radical radiotherapy, with or without concomitant chemotherapy forms the mainstay of organ preservation approaches in mucosal primary head and neck cancer. Despite technical advances in cancer imaging and radiotherapy administration, a significant proportion of patients fail to achieve a complete response to treatment. For those patients who do achieve a complete response, acute and late toxicities remain a cause of morbidity. A critical need therefore exists for imaging biomarkers which are capable of informing patient selection for both treatment intensification and de-escalation strategies.
METHODS/DESIGN: A prospective imaging study has been initiated, aiming to recruit patients undergoing radical radiotherapy (RT) or chemoradiotherapy (CRT) for mucosal primary head and neck cancer (MPHNC). Eligible patients are imaged using FDG-PET/CT before treatment, at the end of week 3 of treatment and 12 weeks after treatment completion according to local imaging policy. Functional MRI using diffusion weighted (DWI), blood oxygen level-dependent (BOLD) and dynamic contrast enhanced (DCE) sequences is carried out prior to, during and following treatment. Information regarding treatment outcomes will be collected, as well as physician-scored and patient-reported toxicity.
The primary objective is to determine the correlation of functional MRI sequences with tumour response as determined by FDG-PET/CT and clinical findings at 12 weeks post-treatment and with local control at 12 months post-treatment. Secondary objectives include prospective correlation of functional MRI and PET imaging with disease-free survival and overall survival, defining the optimal time points for functional MRI assessment of treatment response, and determining the sensitivity and specificity of functional MRI sequences for assessment of potential residual disease following treatment. If the study is able to successfully characterise tumours based on their functional MRI scan characteristics, this would pave the way for further studies refining treatment approaches based on prognostic and predictive imaging data.
Australian New Zealand Clinical Trials Registry (ANZCTR): ACTRN12616000534482 (26 April 2016).
根治性放疗,无论是否联合化疗,都是黏膜原发性头颈癌器官保留治疗方法的主要手段。尽管癌症成像和放疗管理技术取得了进展,但仍有相当一部分患者未能实现对治疗的完全缓解。对于那些实现完全缓解的患者,急性和晚期毒性仍是发病的原因。因此,迫切需要能够为治疗强化和降级策略的患者选择提供信息的成像生物标志物。
方法/设计:一项前瞻性成像研究已经启动,旨在招募接受根治性放疗(RT)或放化疗(CRT)的黏膜原发性头颈癌(MPHNC)患者。符合条件的患者根据当地成像政策在治疗前、治疗第3周结束时和治疗完成后12周使用FDG-PET/CT进行成像。在治疗前、治疗期间和治疗后进行使用扩散加权(DWI)、血氧水平依赖(BOLD)和动态对比增强(DCE)序列的功能磁共振成像。将收集有关治疗结果的信息,以及医生评分和患者报告的毒性。
主要目的是确定功能磁共振成像序列与治疗后12周时FDG-PET/CT和临床发现所确定的肿瘤反应以及治疗后12个月时局部控制之间的相关性。次要目的包括功能磁共振成像和PET成像与无病生存期和总生存期的前瞻性相关性,确定功能磁共振成像评估治疗反应的最佳时间点,以及确定功能磁共振成像序列评估治疗后潜在残留疾病的敏感性和特异性。如果该研究能够根据功能磁共振成像扫描特征成功地对肿瘤进行特征描述,这将为基于预后和预测成像数据改进治疗方法的进一步研究铺平道路。
澳大利亚新西兰临床试验注册中心(ANZCTR):ACTRN12616000534482(2016年4月26日)。