Zhang Wenjia, Liang Xiaolong, Zhang Xinyu, Tong Wei, Shi Guangyuan, Guo Haozhuo, Jin Zhengyu, Tian Jie, Du Yang, Xue Huadan
Department of Radiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No. 1 Shuaifuyuan, Beijing, 100730, China.
Department of Radiology, Peking University People's Hospital, Beijing, 100032, China.
Eur J Nucl Med Mol Imaging. 2024 Jun;51(7):1841-1855. doi: 10.1007/s00259-024-06617-w. Epub 2024 Feb 19.
Pancreatic ductal adenocarcinoma (PDAC) is a lethal hypovascular tumor surrounded by dense fibrosis. Albumin-bound paclitaxel and gemcitabine (AG) chemotherapy is the mainstay of PDAC treatment through depleting peritumoral fibrosis and killing tumor cells; however, it remains challenging due to the lack of a noninvasive imaging method evaluating fibrotic changes during AG chemotherapy. In this study, we developed a dual-modality imaging platform that enables noninvasive, dynamic, and quantitative assessment of chemotherapy-induced fibrotic changes through near-infrared fluorescence molecular imaging (FMI) and magnetic resonance imaging (MRI) using an extradomain B fibronectin (EDB-FN)-targeted imaging probe (ZD2-Gd-DOTA-Cy7).
The ZD2-Gd-DOTA-Cy7 probe was constructed by conjugating a peptide (Cys-TVRTSAD) to Gd-DOTA and the near-infrared dye Cy7. PDAC murine xenograft models were intravenously injected with ZD2-Gd-DOTA-Cy7 at a Gd concentration of 0.05 mmol/kg or free Cy7 and Gd-DOTA as control. The normalized tumor background ratio (TBR) on FMI and the T1 reduction ratio on MRI were quantitatively analyzed. For models receiving AG chemotherapy or saline, MRI/FMI was performed before and after treatment. Histological analyses were performed for validation.
The ZD2-Gd-DOTA-Cy7 concentration showed a linear correlation with the fluorescence intensity and T1 relaxation time in vitro. The optimal imaging time was 30 min after injection of the ZD2-Gd-DOTA-Cy7 (0.05 mmol/kg), only half of the clinic dosage of gadolinium. Additionally, ZD2-Gd-DOTA-Cy7 generated a 1.44-fold and 1.90-fold robust contrast enhancement compared with Cy7 (P < 0.05) and Gd-DOTA (P < 0.05), respectively. For AG chemotherapy monitoring, the T1 reduction ratio and normalized TBR in the fibrotic tumor areas were significantly increased by 1.99-fold (P < 0.05) and 1.78-fold (P < 0.05), respectively, in the control group compared with those in the AG group.
MRI/FMI with a low dose of ZD2-Gd-DOTA-Cy7 enables sensitive imaging of PDAC and the quantitative assessment of fibrotic changes during AG chemotherapy, which shows potential clinical applications for precise diagnosis, post-treatment monitoring, and disease management.
胰腺导管腺癌(PDAC)是一种致命的低血供肿瘤,周围环绕着致密的纤维化组织。白蛋白结合型紫杉醇和吉西他滨(AG)化疗是PDAC治疗的主要手段,通过消除肿瘤周围纤维化并杀死肿瘤细胞来实现;然而,由于缺乏一种在AG化疗期间评估纤维化变化的非侵入性成像方法,这一治疗仍然具有挑战性。在本研究中,我们开发了一种双模态成像平台,该平台能够通过使用一种靶向域外B纤连蛋白(EDB-FN)的成像探针(ZD2-Gd-DOTA-Cy7),借助近红外荧光分子成像(FMI)和磁共振成像(MRI)对化疗诱导的纤维化变化进行非侵入性、动态和定量评估。
ZD2-Gd-DOTA-Cy7探针是通过将一种肽(Cys-TVRTSAD)与Gd-DOTA和近红外染料Cy7偶联构建而成。将ZD2-Gd-DOTA-Cy7以0.05 mmol/kg的Gd浓度静脉注射到PDAC小鼠异种移植模型中,以游离的Cy7和Gd-DOTA作为对照。对FMI上的标准化肿瘤背景比率(TBR)和MRI上的T1降低比率进行定量分析。对于接受AG化疗或生理盐水的模型,在治疗前后进行MRI/FMI检查。进行组织学分析以进行验证。
ZD2-Gd-DOTA-Cy7浓度在体外与荧光强度和T1弛豫时间呈线性相关。最佳成像时间为注射ZD2-Gd-DOTA-Cy7(0.05 mmol/kg)后30分钟,仅为临床钆剂量的一半。此外,与Cy7(P < 0.05)和Gd-DOTA(P < 0.05)相比,ZD2-Gd-DOTA-Cy7分别产生了1.44倍和1.90倍的显著对比增强。对于AG化疗监测,与AG组相比,对照组纤维化肿瘤区域的T1降低比率和标准化TBR分别显著增加了1.99倍(P < 0.05)和1.78倍(P < 0.05)。
低剂量ZD2-Gd-DOTA-Cy7的MRI/FMI能够对PDAC进行灵敏成像,并对AG化疗期间的纤维化变化进行定量评估,这显示出在精确诊断、治疗后监测和疾病管理方面的潜在临床应用价值。