[18F]FSPG-PET provides an early marker of radiotherapy response in head and neck squamous cell cancer

Khrishanthne Sambasivan, Will E. Tyrrell, Rizwan Farooq, Jenasee Mynerich, Richard S. Edwards, Muhammet Tanc, Teresa Guerrero Urbano, Timothy H. Witney
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Abstract

The ability to image early treatment response to radiotherapy in head and neck squamous cell carcinoma (HNSCC) will enable the identification of radioresistant tumor volumes suitable for treatment intensification. Here, we propose the system xc− radiotracer (4S)-4-(3-[18F]fluoropropyl)-L-glutamate ([18F]FSPG) as a non-invasive method to monitor radiation response in HNSCC. We assessed temporal changes in cell death, antioxidant status, and [18F]FSPG retention following a single dose of 10 Gy irradiation in FaDU HNSCC cells. Next, using a fractionated course of radiotherapy, we assessed tumor volume changes and performed [18F]FSPG-PET imaging in FaDU-bearing mouse xenografts, followed by ex vivo response assessment. In cells, 10 Gy irradiation reduced [18F]FSPG retention, coinciding with the induction of apoptosis and the production of reactive oxygen species. In vivo, [18F]FSPG tumor retention was halved seven days after the start of treatment, which preceded radiotherapy-induced tumor shrinkage, thereby confirming [18F]FSPG-PET as an early and sensitive marker of radiation response.

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[18F]FSPG-PET是头颈部鳞状细胞癌放疗反应的早期标志物。
对头颈部鳞状细胞癌(HNSCC)放疗的早期治疗反应进行成像的能力将有助于识别适合强化治疗的抗放射肿瘤体积。在这里,我们提出用 xc - 放射性示踪剂 (4S)-4-(3-[18F]fluoropropyl)-L -谷氨酸([18F]FSPG)系统作为监测 HNSCC 放射反应的非侵入性方法。我们评估了FaDU HNSCC细胞在单剂量10 Gy照射后细胞死亡、抗氧化状态和[18F]FSPG保留的时间变化。接下来,我们采用分次放疗的方法,评估了肿瘤体积的变化,并对FaDU小鼠异种移植进行了[18F]FSPG-PET成像,然后进行了体内外反应评估。在细胞中,10 Gy 照射减少了[18F]FSPG 的保留,这与诱导凋亡和活性氧的产生相吻合。在体内,[18F]FSPG 的肿瘤保留率在治疗开始七天后减半,这比放疗引起的肿瘤缩小更早,从而证实[18F]FSPG-PET 是辐射反应的早期敏感标记物。
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