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Internal dosimetry and biodistribution of indigenously prepared 177Lu-DOTA-rituximab in lymphoma and other hematological malignancies treated with rituximab

医学 核医学 剂量学 美罗华 多塔 体内分布 淋巴瘤 放射免疫疗法 骨髓 内科学 化学 单克隆抗体 抗体 免疫学 体外 螯合作用 生物化学 有机化学
作者
Yeshwanth Edamadaka,Rahul V. Parghane,Sudeep Sahu,Sangita Lad,Kamaldeep Kamaldeep,Gaurav Wanage,Chandrakala Shanmukhaiah,Vrinda Kulkarni,Sandip Basu
出处
期刊:Nuclear Medicine Communications [Lippincott Williams & Wilkins]
卷期号:45 (10): 823-834 被引量:1
标识
DOI:10.1097/mnm.0000000000001875
摘要

Objective The aim of this study was to evaluate the biodistribution and dosimetry of lutetium-177-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid ( 177 Lu-DOTA)-rituximab in CD20 + non-Hodgkin’s lymphoma and other hematological malignancies treated with rituximab. Methods The standard dosimetry protocol was used, with cold rituximab infusion, then a diagnostic activity of 177 Lu-DOTA-rituximab. Planar images were acquired at multiple time points. Normal organs and tumor dosimetry were performed by using organ and tumor-specific regions of interest and whole-body counts were obtained serially after pixel matched, background, scatter, and attenuation correction. The mean radiation absorbed doses were obtained from OLINDA/EXM v2.1.1 and ORIGIN software. Results A total of 22 patients were included in this study. Prolonged blood pool clearance of 177 Lu-DOTA-rituximab with long residence time in the blood pool and normal organs were observed. The whole body effective half-life was 104.5 ± 22 h. The mean total body radiation absorbed dose was 0.208 ± 0.03 mGy/MBq and the mean total body effective dose was 0.196 ± 0.05 mGy/MBq of 177 Lu-DOTA-rituximab. The mean radiation absorbed doses of 0.613 ± 0.21, 1.68 ± 2, 1.01 ± 0.42, and 0.136 ± 0.02mGy/MBq were seen for the liver, spleen, kidneys, and bone marrow, respectively. Tumor lesion uptake was noticed in two patients with tumor radiation absorbed doses were 0.842 mGy/MBq in one and 9.9 mGy/MBq in the other patient. A strong correlation was obtained between the cumulative activities of radiation-absorbed doses derived from ORIGIN and OLINDA software methods at a significant P value less than 0.001. Conclusion The results of our study demonstrated favorable biodistribution and dosimetry of indigenously produced 177 Lu-DOTA-rituximab in patients with CD20 + lymphoma. These results can be used for future studies of radioimmunotherapy employing 177 Lu-DOTA-rituximab.

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