Dubec Michael J, Price James, Berks Michael, Gaffney John, Little Ross A, Porta Nuria, Sridharan Nivetha, Datta Anubhav, McHugh Damien J, Hague Christina J, Cheung Susan, Manoharan Prakash, van Herk Marcel, Choudhury Ananya, Matthews Julian C, Parker Geoff J M, Buckley David L, Harrington Kevin J, McPartlin Andrew, O'Connor James P B
Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Christie Medical Physics and Engineering, The Christie NHS Foundation Trust, Manchester, United Kingdom.
Clin Cancer Res. 2024 Dec 16;30(24):5620-5629. doi: 10.1158/1078-0432.CCR-24-1170.
Hypoxia mediates treatment resistance in solid tumors. We evaluated if oxygen-enhanced MRI-derived hypoxic volume (HVMRI) is repeatable and can detect radiotherapy-induced hypoxia modification in human papillomavirus-associated oropharyngeal head and neck squamous cell cancer.
A total of 27 patients were recruited prospectively between March 2021 and January 2024. HVMRI was measured in primary and nodal tumors prior to standard-of-care (chemo)radiotherapy and then at weeks 2 and 4 (W2 and W4) into therapy. Two pretreatment scans assessed biomarker within-subject coefficient of variation and repeatability coefficient (RC). Cohort treatment response was measured using mixed-effects modeling. Responding lesions were identified by comparing HVMRI change with RC limits of agreement.
Oxygen-enhanced MRI identified hypoxia in all lesions. The HVMRI within-subject coefficient of variation was 24.6%, and RC limits of agreement were -45.7% to 84.1%. A cohort median pretreatment HVMRI of 11.3 cm3 reduced to 6.9 cm3 at W2 and 5.9 cm3 at W4 (both P < 0.001). HVMRI was reduced in 54.5% of individual lesions by W2 and in 88.2% by W4. All lesions with W2 hypoxia reduction showed persistent modification at W4. HVMRI reduced in some lesions that showed no overall volume change. Hypoxia modification was discordant between primary and nodal tumors in 50.0% of patients.
Radiation-induced hypoxia modification can occur as early as W2, but onset varies between patients and was not necessarily associated with overall size change. Half of all patients had discordant changes in primary and nodal tumors. These findings have implications for patient selection and timing of dose de-escalation strategies in human papillomavirus-associated oropharyngeal carcinoma. See related commentary by Mason, p. 5503.
缺氧介导实体瘤的治疗抵抗。我们评估了基于氧增强磁共振成像(MRI)得出的缺氧体积(HVMRI)是否具有可重复性,以及能否检测人乳头瘤病毒相关的口咽头颈鳞状细胞癌放疗引起的缺氧变化。
2021年3月至2024年1月期间前瞻性招募了27例患者。在标准(化疗)放疗前以及治疗第2周和第4周(W2和W4)测量原发肿瘤和淋巴结转移瘤的HVMRI。两次治疗前扫描评估了生物标志物的受试者内变异系数和重复性系数(RC)。使用混合效应模型测量队列治疗反应。通过将HVMRI变化与RC一致性界限进行比较来确定有反应的病变。
氧增强MRI在所有病变中均识别出缺氧。HVMRI的受试者内变异系数为24.6%,RC一致性界限为-45.7%至84.1%。队列治疗前HVMRI的中位数为11.3 cm³,在W2时降至6.9 cm³,在W4时降至5.9 cm³(均P < 0.001)。到W2时,54.5%的个体病变HVMRI降低,到W4时为88.2%。所有在W2时缺氧减少的病变在W4时均显示持续变化。一些总体积无变化的病变HVMRI也降低。50.0%的患者原发肿瘤和淋巴结转移瘤之间的缺氧变化不一致。
放疗引起的缺氧变化最早可在W2出现,但不同患者的发病时间不同,且不一定与总体大小变化相关。所有患者中有一半原发肿瘤和淋巴结转移瘤出现不一致的变化。这些发现对人乳头瘤病毒相关口咽癌患者的选择和剂量降低策略的时机具有重要意义。见梅森的相关评论,第5503页。