School of Biomedical Engineering & Imaging Sciences Clinical Academic Group, King's College London, London, UK.
Department of Radiology, Guy's and St Thomas' Hospital, London, UK.
Eur Radiol. 2021 Dec;31(12):9273-9286. doi: 10.1007/s00330-021-07913-x. Epub 2021 May 19.
To investigate the optimal timing for post-chemoradiotherapy (CRT) reference magnetic resonance imaging (MRI) in head and neck cancer, so as to demonstrate a maximal treatment response. To assess whether this differs in human papillomavirus-related oropharyngeal cancer (HPV-OPC) and whether the MRI timing impacts on the ability to predict treatment success.
Following ethical approval and informed consent, 45 patients (40 male, mean age 59.7 ± 7.9 years, 33 HPV-OPC) with stage 3 and 4 HNSCC underwent pre-treatment, 6- and 12-week post-CRT MRIs in this prospective cohort study. Primary tumour (n = 39) size, T2w morphology and diffusion weight imaging (DWI) scores, together with nodal (n = 42) size and necrotic/cystic change, were recorded. Interval imaging changes were analysed for all patients and according to HPV-OPC status. MRI descriptors and their interval changes were also compared with 2-year progression-free survival (PFS).
All MRI descriptors significantly changed between pre-treatment and 6-week post-treatment MRI studies (p < .001). Primary tumour and nodal volume decreased between 6- and 12-week studies; however, interval changes in linear dimensions were only evident for HPV-OPC lymph nodes. Nodal necrosis scores also evolved after 6 weeks but other descriptors were stable. The 6-week nodal necrosis score and the 6- and 12-week nodal volume were predictive of 2-year PFS.
Apart from HPV-OPC patients with nodal disease, the 6-week post-CRT MRI demonstrates maximal reduction in the linear dimensions of head and neck cancer; however, a later reference study should be considered if volumetric analysis is applied.
• This study provides guidance on when early post-treatment imaging should be performed in head and neck cancer following chemoradiotherapy, in order to aid subsequent detection of recurrent tumour. • Lymph nodes in HPV-related oropharyngeal cancer patients clearly reduced in size from 6 to 12 weeks post-treatment. However, other lymph node disease and all primary tumours showed only a minor reduction in size beyond 6 weeks, and this required a detailed volumetric analysis for demonstration. • Timing of the reference MRI following chemoradiotherapy for head and neck cancer depends on whether the patient has HPV-related oropharyngeal cancer and whether there is nodal disease. MRI as early as 6 weeks post-treatment may be performed unless volumetric analysis is routinely performed.
探讨头颈部癌放化疗后(CRT)参考磁共振成像(MRI)的最佳时机,以显示最大的治疗反应。评估 HPV 相关口咽癌(HPV-OPC)是否存在差异,以及 MRI 时机是否影响预测治疗成功的能力。
本前瞻性队列研究经伦理批准和知情同意后,入组 45 例(男 40 例,平均年龄 59.7 ± 7.9 岁,HPV-OPC 33 例)局部晚期头颈部鳞癌患者。所有患者均接受了治疗前、6 周和 12 周 CRT MRI。记录了原发肿瘤(n=39)大小、T2w 形态和弥散加权成像(DWI)评分,以及淋巴结(n=42)大小和坏死/囊性改变。对所有患者和 HPV-OPC 患者进行了间隔成像变化分析。还将 MRI 描述符及其间隔变化与 2 年无进展生存率(PFS)进行了比较。
所有 MRI 描述符在治疗前和 6 周治疗后 MRI 研究之间均有显著变化(p<0.001)。原发肿瘤和淋巴结体积在 6 周和 12 周研究之间减少;然而,HPV-OPC 淋巴结的线性尺寸间隔变化仅明显。淋巴结坏死评分在 6 周后也有变化,但其他描述符保持稳定。6 周时的淋巴结坏死评分和 6 周和 12 周时的淋巴结体积是 2 年 PFS 的预测因素。
除了 HPV-OPC 患者的淋巴结疾病外,CRT 后 6 周的 MRI 显示头颈部癌症的线性尺寸最大减少;然而,如果应用体积分析,应考虑进行更晚的参考研究。
本研究提供了在头颈部癌放化疗后何时进行早期治疗后成像的指导,以帮助随后检测肿瘤复发。
HPV 相关口咽癌患者的淋巴结在治疗后 6 至 12 周明显缩小。然而,其他淋巴结疾病和所有原发肿瘤的大小仅在 6 周后略有缩小,需要进行详细的体积分析才能显示。
头颈部癌放化疗后参考 MRI 的时间取决于患者是否患有 HPV 相关口咽癌以及是否存在淋巴结疾病。除非常规进行体积分析,否则可能在治疗后 6 周进行 MRI。