[Theranostics of osteosarcoma and lung metastasis with new integrin α β receptor targeted radiotracers].

Objective: To investigate the value of integrin α β targeted microPET/CT imaging with Ga-NODAGA-RGD as radiotracer for the detection of osteosarcoma and theranostics of osteosarcoma lung metastasis.

Methods: The Ga-NODAGA-RGD and Lu-NODAGA-RGD were prepared via one-step method and their stability and integrin α β binding specificity were investigated . Forty-one nude mice were injected with human MG63 osteosarcoma to established the animal model bearing subcutaneous osteosarcoma ( =21), osteosarcoma in tibia ( =5), and osteosarcoma pulmonary metastatic ( =15). The microPET-CT imaging was carried out in 3 animal models at 1 hour after tail vein injection of Ga-NODAGA-RGD . Biodistribution study of Ga-NODAGA-RGD was performed in animal model bearing subcutaneous osteosarcoma at 10, 60, and 120 minutes. The animal model bearing pulmonary metastatic osteosarcoma was injected with Lu-NODAGA-RGD at 7 weeks after model establishment to observe the therapeutic effect of pulmonary metastatic osteosarcoma. Histological and immunohistochemistry examinations were also done to confirm the establishment of animal model and integrin β expression in animal models bearing subcutaneous osteosarcoma and bearing pulmonary metastatic osteosarcoma.

Results: Ga-NODAGA-RGD and Lu-NODAGA-RGD had good stability with the 50% inhibitory concentration value of (5.0±1.1) and (6.5±0.8) nmol/L, respectively. The radiochemical purity of Ga-NODAGA-RGD at 1, 4, and 8 hours was 98.5%±0.3%, 98.3%±0.5%, and 97.9%±0.4%; while the radiochemical purity of Lu-NODAGA-RGD at 1, 7, and 14 days was 99.3%±0.7%, 98.7%±1.2%, and 96.0%±2.8%. Ga-NODAGA-RGD microPET-CT showed that the accumulation of Ga-NODAGA-RGD in animal models bearing subcutaneous osteosarcoma and osteosarcoma in tibia and in lung metastasis as small as 1-2 mm in diameter of animal model bearing pulmonary metastatic osteosarcoma. Biodistribution study of Ga-NODAGA-RGD in animal model bearing subcutaneous osteosarcoma revealed rapid clearance from blood with tumor peak uptake of (3.85±0.84) %ID/g at 120 minutes. The distribution of Lu-NODAGA-RGD in lung metastasis was similar with Ga-NODAGA-RGD . The number and size of osteosarcoma metastasis decreased at 2 weeks after Lu-NODAGA-RGD administration and integrin targeting specificity was confirmed by pathology examination.

Conclusion: Ga-NODAGA-RGD was potential for positive imaging and early detection of osteosarcoma and metastasis. Targeted radiotherapy with Lu-NODAGA-RGD was one potential alternative for osteosarcoma lung metastasis.