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用于多发性骨髓瘤和淋巴瘤CD38靶向免疫正电子发射断层显像的锆-去铁胺-isatuximab

Zr-DFO-Isatuximab for CD38-Targeted ImmunoPET Imaging of Multiple Myeloma and Lymphomas.

作者信息

Herrero Alvarez Natalia, Michel Alexa L, Viray Tara D, Mayerhoefer Marius E, Lewis Jason S

机构信息

Department of Radiology and Program in Pharmacology, Memorial Sloan Kettering Cancer Center, New York, New York 10065, United States.

Departments of Pharmacology and Radiology, Weill Cornell Medicine, New York, New York 10065, United States.

出版信息

ACS Omega. 2023 Apr 11;8(25):22486-22495. doi: 10.1021/acsomega.3c00624. eCollection 2023 Jun 27.

Abstract

Multiple myeloma (MM) is the second most prevalent hematological malignancy. It remains incurable despite the availability of novel therapeutic approaches, marking an urgent need for new agents for noninvasive targeted imaging of MM lesions. CD38 has proven to be an excellent biomarker due to its high expression in aberrant lymphoid and myeloid cells relative to normal cell populations. Using isatuximab (Sanofi), the latest FDA-approved CD38-targeting antibody, we have developed Zirconium-89(Zr)-labeled isatuximab as a novel immunoPET tracer for the delineation of MM and evaluated the extension of its applicability to lymphomas. studies validated the high binding affinity and specificity of Zr-DFO-isatuximab for CD38. PET imaging demonstrated the high performance of Zr-DFO-isatuximab as a targeted imaging agent to delineate tumor burden in disseminated models of MM and Burkitt's lymphoma. biodistribution studies confirmed that high accumulations of the tracer in bone marrow and bone skeleton correspond to specific disease lesions as they are reduced to background in blocking and healthy controls. This work demonstrates the promise of Zr-DFO-isatuximab as an immunoPET tracer for CD38-targeted imaging of MM and certain lymphomas. More importantly, its potential as an alternative to Zr-DFO-daratumumab holds great clinical relevance.

摘要

多发性骨髓瘤(MM)是第二常见的血液系统恶性肿瘤。尽管有新的治疗方法,但它仍然无法治愈,这表明迫切需要用于MM病变无创靶向成像的新药物。CD38已被证明是一种出色的生物标志物,因为相对于正常细胞群体,它在异常淋巴细胞和髓细胞中高表达。使用最新获得美国食品药品监督管理局(FDA)批准的靶向CD38的抗体isatuximab(赛诺菲),我们开发了锆-89(Zr)标记的isatuximab作为一种新型免疫正电子发射断层显像(immunoPET)示踪剂,用于描绘MM,并评估其在淋巴瘤中的适用性扩展。研究验证了Zr-DFO-isatuximab对CD38具有高结合亲和力和特异性。PET成像证明Zr-DFO-isatuximab作为一种靶向成像剂,在MM和伯基特淋巴瘤的播散模型中描绘肿瘤负荷方面具有高性能。生物分布研究证实,示踪剂在骨髓和骨骼中的高积聚对应于特定的疾病病变,因为在阻断和健康对照中它们会降至背景水平。这项工作证明了Zr-DFO-isatuximab作为用于MM和某些淋巴瘤的CD38靶向成像的免疫正电子发射断层显像示踪剂的前景。更重要的是,它作为Zr-DFO-达雷妥尤单抗替代品的潜力具有重大临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2472/10308590/838385b5d0b4/ao3c00624_0001.jpg

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