期刊
MOLECULAR PHARMACEUTICS
卷 20, 期 3, 页码 1788-1795出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.2c00978
关键词
bone metastasis; radionuclide therapy; 177Lu-DOTA-IBA; ibandronate
A new bisphosphonate radiopharmaceutical, Lu-177-DOTA-IBA, was synthesized and studied for targeted diagnosis and treatment of bone metastases. It exhibited good biological properties and safety, with promising results in a preliminary clinical translation study.
Bone metastases of malignant tumors significantly threaten the patient survival and quality of life. We designed and synthesized a novel bisphosphonate radiopharmaceutical [68Ga- or targeted diagnosis and treatment of bone metastases. This study explored the basic biological characteristics of Lu-177-DOTA-IBA, guiding clinical translation and providing evidence for future clinical applications. The control variable method was used to optimize the optimal labeling conditions. The in vitro properties, biological distribution, and toxicity of Lu-177-DOTA-IBA were studied. Normal mice and tumor-bearing mice were imaged using micro SPECT/CT. With Ethics Committee approval, five volunteers were recruited for a preliminary clinical translation study. Lu-177-DOTA-IBA has a radiochemical purity of more than 98%, with good biological properties and safety. Blood clearance is fast and soft tissue uptake is low. Tracers are excreted mainly through the urinary system, targeting and continuously concentrating in the bones. Three patients experienced significant pain relief within 3 days after Lu-177-DOTA-IBA treatment (740-1110 MBq), lasting more than 2 months, with no toxic side effects. Lu-177-DOTA-IBA is easy to prepare and exhibits good pharmacokinetic characteristics. Low-dose Lu-177-DOTA-IBA is effective, well tolerated, and was associated with no significant adverse reactions. It is a promising radiopharmaceutical for the targeted treatment of bone metastases, controlling the progress of bone metastasis and improving survival and quality of life of patients with advanced bone metastasis.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据