Graduate Biomedical Sciences, University of Alabama at Birmingham, Birmingham, Alabama.
School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Mol Cancer Ther. 2020 Sep;19(9):1922-1929. doi: 10.1158/1535-7163.MCT-19-0819. Epub 2020 Jun 30.
Maximal safe resection of malignant tissue is associated with improved progression-free survival and better response to radiation and chemotherapy for patients with glioblastoma (GBM). 5-Aminolevulinic acid (5-ALA) is the current FDA-approved standard for intraoperative brain tumor visualization. Unfortunately, autofluorescence in diffuse areas and high fluorescence in dense tissues significantly limit discrimination at tumor margins. This study is the first to compare 5-ALA to an investigational new drug, panitumumab-IRDye800CW, in the same animal model. A patient-derived GBM xenograft model was established in 16 nude mice, which later received injections of 5-ALA, panitumumab-IRDye800CW, IRDye800CW, 5-ALA and IRDye800CW, or 5-ALA and panitumumab-IRDye800CW. Brains were prepared for multi-instrument fluorescence imaging, IHC, and quantitative analysis of tumor-to-background ratio (TBR) and tumor margin accuracy. Statistical analysis was compared with Wilcoxon rank-sum or paired test. Panitumumab-IRDye800CW had a 30% higher comprehensive TBR compared with 5-ALA ( = 0.0079). SDs for core and margin regions of interest in 5-ALA-treated tissues were significantly higher than those found in panitumumab-IRDye800CW-treated tissues ( = 0.0240 and = 0.0284, respectively). Panitumumab-IRDye800CW specificities for tumor core and margin were more than 10% higher than those of 5-ALA. Higher AUC for panitumumab-IRDye800CW indicated strong capability to discriminate between normal and malignant brain tissue when compared with 5-ALA. This work demonstrates that panitumumab-IRDye800CW shows potential as a targeting agent for fluorescence intraoperative detection of GBM. Improved margin definition and surgical resection using panitumumab-IRDye800 has the potential to improve surgical outcomes and survival in patients with GBM compared with 5-ALA.
最大限度地安全切除恶性组织与患者胶质母细胞瘤(GBM)无进展生存期的改善和对放化疗的更好反应相关。5-氨基酮戊酸(5-ALA)是目前美国食品和药物管理局(FDA)批准的用于术中脑肿瘤可视化的标准。不幸的是,弥漫区域的自发荧光和致密组织中的高荧光显著限制了肿瘤边界的区分。这项研究首次在相同的动物模型中将 5-ALA 与一种研究性新药帕尼单抗-IRDye800CW 进行了比较。在 16 只裸鼠中建立了一个患者来源的 GBM 异种移植模型,随后给这些裸鼠注射 5-ALA、帕尼单抗-IRDye800CW、IRDye800CW、5-ALA 和 IRDye800CW 或 5-ALA 和帕尼单抗-IRDye800CW。为多仪器荧光成像、免疫组化和肿瘤与背景比(TBR)和肿瘤边界准确性的定量分析制备大脑。统计分析采用 Wilcoxon 秩和检验或配对检验进行比较。与 5-ALA 相比,帕尼单抗-IRDye800CW 的综合 TBR 高 30%( = 0.0079)。5-ALA 处理组织的核心和边缘感兴趣区域的标准差明显高于帕尼单抗-IRDye800CW 处理组织( = 0.0240 和 = 0.0284)。帕尼单抗-IRDye800CW 对肿瘤核心和边缘的特异性比 5-ALA 高 10%以上。与 5-ALA 相比,panitumumab-IRDye800CW 的 AUC 更高,表明其具有很强的能力来区分正常和恶性脑组织。这项工作表明,panitumumab-IRDye800CW 作为一种针对 GBM 荧光术中检测的靶向剂具有潜力。与 5-ALA 相比,使用 panitumumab-IRDye800 进行更精确的边界定义和手术切除,有可能改善 GBM 患者的手术结果和生存率。