PET Center, Huashan Hospital, Fudan University, Shanghai, 200235, China.
PET/CT Center, The First People's Hospital of Yunnan Province, Kunming, 650032, Yunnan, China.
Eur Radiol. 2023 Oct;33(10):7077-7088. doi: 10.1007/s00330-023-09679-w. Epub 2023 May 11.
Pancreatic ductal adenocarcinoma (PDAC) is a highly malignant solid tumor that lacks early diagnostic methods. Recently, targeted immunotherapy and radiotherapy have been integrated with radionuclide-antibody conjugate drugs, which can be used for targeted diagnosis and dynamic imaging of tumors. CEACAM6 is overexpressed in pancreatic tumors and is a potential theranostic target for PDAC. We aimed to develop a novel targeted carrier for theranostics of PDAC and other solid tumors.
Based on camelid heavy-chain-only antibodies, we developed a CEACAM6-targeting recombinant antibody NY004, and evaluated it as a novel antibody-carrier for imaging and therapy of cancer in tumor models. We labeled NY004 with theranostic nuclides and applied this self-developed antibody platform in diagnostic imaging and antitumor assessment in PDAC models.
Through microPET, IHC, and biodistribution assays, targeting and biodistribution of [Zr]-NY004 in solid tumors including PDAC was examined, and the investigated tumors were all CEACAM6-positive malignancies. We found that NY004 was suitable for use as a drug carrier for radioimmunotheranostics. Our study showed that NY004 was characterized by high targeted uptake and a long retention time in PANC-1 tumors (up to 6 days post-injection), with good specificity and high imaging efficiency. Therapeutic evaluation of the radionuclide-labeled antibody drug [Lu]-NY004 in PDAC tumor-bearing model revealed that NY004 had high and prolonged uptake in tumors, relatively low non-target organ uptake, and good anti-tumor efficacy.
As a drug platform for radiotheranostics, CEACAM6-specific antibody NY004 met the requirements of easy-labeling, targeting specificity, and effective persistence in pancreatic adenocarcinoma tissues.
• [Zr]-NY004 has good specificity and high imaging efficiency, and is characterized by high tumor-targeting uptake and a long tumor retention time as a PET molecular imaging tracer. • Therapeutic radionuclide-conjugated antibody drug [Lu]-NY004 has high uptake and prolonged uptake duration in tumors, low non-target organ uptake, and significant tumor-inhibiting efficacy in PDAC model. • The self-developed antibody structure NY004 is a promising drug platform for radioimmunotheranostics of CEACAM6-positive tumors including pancreatic ductal adenocarcinoma.
胰腺导管腺癌(PDAC)是一种高度恶性的实体肿瘤,缺乏早期诊断方法。最近,靶向免疫疗法和放射疗法已与放射性核素-抗体偶联药物相结合,可用于肿瘤的靶向诊断和动态成像。CEACAM6 在胰腺肿瘤中过表达,是 PDAC 的潜在治疗和诊断靶点。我们旨在开发一种新型的靶向载体,用于 PDAC 和其他实体肿瘤的治疗和诊断。
基于骆驼科重链抗体,我们开发了一种靶向 CEACAM6 的重组抗体 NY004,并将其评估为用于癌症成像和治疗的新型抗体载体,在肿瘤模型中进行了成像和治疗评估。我们用治疗诊断核素标记 NY004,并将这种自行开发的抗体平台应用于 PDAC 模型中的诊断成像和抗肿瘤评估。
通过 microPET、免疫组化和生物分布实验,研究了[Zr]-NY004 在包括 PDAC 在内的实体瘤中的靶向性和生物分布,研究的肿瘤均为 CEACAM6 阳性恶性肿瘤。我们发现 NY004 适合用作放射性免疫治疗药物载体。我们的研究表明,NY004 具有高靶向摄取和在 PANC-1 肿瘤中长时间滞留的特点(注射后长达 6 天),具有良好的特异性和高成像效率。在 PDAC 肿瘤荷瘤模型中对放射性标记抗体药物[Lu]-NY004 的治疗评估表明,NY004 在肿瘤中有高摄取和长时间摄取,非靶器官摄取相对较低,具有良好的抗肿瘤疗效。
作为放射治疗药物平台,CEACAM6 特异性抗体 NY004 满足易于标记、靶向特异性和在胰腺腺癌组织中有效持续的要求。
•[Zr]-NY004 具有良好的特异性和高成像效率,作为 PET 分子成像示踪剂,其特点是具有高肿瘤靶向摄取和长肿瘤保留时间。•治疗性放射性核素缀合抗体药物[Lu]-NY004 在 PDAC 模型中具有高摄取和长时间摄取持续时间、低非靶器官摄取和显著的肿瘤抑制疗效。•自行开发的抗体结构 NY004 是一种有前途的用于治疗包括胰腺导管腺癌在内的 CEACAM6 阳性肿瘤的放射免疫治疗药物平台。