Department of Radiology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA.
Department of Otorhinolaryngology and Head and Neck Surgery, Federal University of São Paulo, São Paulo, Brazil.
Eur J Nucl Med Mol Imaging. 2021 Oct;48(11):3618-3630. doi: 10.1007/s00259-021-05372-6. Epub 2021 May 5.
Visual inspection and biopsy is the current standard of care for oral cancer diagnosis, but is subject to misinterpretation and consequently to misdiagnosis. Topically applied PARPi-FL is a molecularly specific, fluorescent contrast-based approach that may fulfill the unmet need for a simple, in vivo, non-invasive, cost-effective, point-of-care method for the early diagnosis of oral cancer. Here, we present results from a phase I safety and feasibility study on fluorescent, topically applied PARPi-FL. Twelve patients with a histologically proven oral squamous cell carcinoma (OSCC) gargled a PARPi-FL solution for 60 s (15 mL, 100 nM, 250 nM, 500 nM, or 1000 nM), followed by gargling a clearing solution for 60 s. Fluorescence measurements of the lesion and surrounding oral mucosa were taken before PARPi-FL application, after PARPi-FL application, and after clearing. Blood pressure, oxygen levels, clinical chemistry, and CBC were obtained before and after tracer administration.
PARPi-FL was well-tolerated by all patients without any safety concerns. When analyzing the fluorescence signal, all malignant lesions showed a significant differential in contrast after administration of PARPi-FL, with the highest increase occurring at the highest dose level (1000 nM), where all patients had a tumor-to-margin fluorescence signal ratio of >3. A clearing step was essential to increase signal specificity, as it clears unbound PARPi-FL trapped in normal anatomical structures. PARPi-FL tumor cell specificity was confirmed by ex vivo tabletop confocal microscopy. We have demonstrated that the fluorescence signal arose from the nuclei of tumor cells, endorsing our macroscopic findings.
A PARPi-FL swish & spit solution is a rapid and non-invasive diagnostic tool that preferentially localizes fluorescent contrast to OSCC. This technique holds promise for the early detection of OSCC based on in vivo optical evaluation and targeted biopsy of suspicious lesions in the oral cavity.
Clinicaltrials.gov -NCT03085147, registered on March 21st, 2017.
目视检查和活检是目前口腔癌诊断的标准护理方法,但存在误诊的风险。局部应用 PARPi-FL 是一种分子特异性、荧光对比的方法,可能满足对简单、体内、非侵入性、具有成本效益、即时护理的口腔癌早期诊断方法的未满足需求。在这里,我们介绍了一项关于荧光局部应用 PARPi-FL 的 I 期安全性和可行性研究的结果。12 名经组织学证实的口腔鳞状细胞癌 (OSCC) 患者用 PARPi-FL 溶液漱口 60 秒(15 毫升,100 纳米,250 纳米,500 纳米或 1000 纳米),然后再漱口 60 秒。在 PARPi-FL 应用前、应用后和冲洗后,对病变和周围口腔黏膜进行荧光测量。在示踪剂给药前后获得血压、氧水平、临床化学和 CBC。
所有患者均耐受良好,无任何安全问题。在分析荧光信号时,所有恶性病变在 PARPi-FL 给药后均显示出明显的对比度差异,在最高剂量水平(1000 纳米)下,所有患者的肿瘤与边缘荧光信号比均>3。冲洗步骤对于提高信号特异性是必不可少的,因为它可以清除被困在正常解剖结构中的未结合的 PARPi-FL。PARPi-FL 的肿瘤细胞特异性通过离体台式共聚焦显微镜得到证实。我们已经证明,荧光信号来自肿瘤细胞的细胞核,这支持了我们的宏观发现。
PARPi-FL 漱口液是一种快速、非侵入性的诊断工具,它优先将荧光对比度定位到 OSCC。该技术有望通过对口腔可疑病变进行体内光学评估和靶向活检,实现 OSCC 的早期检测。
Clinicaltrials.gov-NCT03085147,于 2017 年 3 月 21 日注册。