Clin Nucl Med. 2023 Jun 1;48(6):489-496. doi: 10.1097/RLU.0000000000004634. Epub 2023 Mar 26.
We designed and synthesized a novel theranostic bisphosphonate radiopharmaceutical ( 68 Ga- or 177 Lu-labeled DOTA-ibandronic acid [ 68 Ga/ 177 Lu-DOTA-IBA]) for bone metastasis. In this study, the dosimetry, safety, and efficacy of 68 Ga/ 177 Lu-DOTA-IBA as a theranostic radiopharmaceutical for bone metastases were evaluated in patients with malignancy based on 68 Ga- and 177 Lu-DOTA-IBA images, blood samples, and dosimetric analysis.
Eighteen patients with bone metastasis and progression under conventional therapies were included in this study. Baseline 99m Tc-MDP SPECT and 68 Ga-DOTA-IBA PET/CT were performed for comparative purposes within 3 days. After receiving 891.5 ± 301.3 MBq 177 Lu-DOTA-IBA, serial 177 Lu-DOTA-IBA SPECT bone scan was performed over 14 days. Dosimetric evaluation was performed for main organs and tumor lesions. Safety was assessed by blood biomarkers. Karnofsky Performance Status, pain score, and follow-up 68 Ga-DOTA-IBA PET/CT were performed for response evaluation.
Baseline 68 Ga-DOTA-IBA PET demonstrated a higher efficacy for detecting bone metastases compared with 99m Tc-MDP SPECT. The time-activity curves showed fast uptake and high retention of 177 Lu-DOTA-IBA in bone metastases (24 hours: 9.43 ± 2.75 %IA; 14 days: 5.45 ± 2.52 %IA). Liver, kidneys, and red marrow time-activity curves revealed a low uptake and fast clearance. The radiation-absorbed dose in bone metastasis lesions (6.40 ± 2.13 Gy/GBq) was significantly higher than that in red marrow (0.47 ± 0.19 Gy/GBq), kidneys (0.56 ± 0.19 Gy/GBq), or liver (0.28 ± 0.07 Gy/GBq), with all P 's < 0.001. Compared with baseline level, only one patient developed new grade 1 leukopenia (toxicity rate, 6%). The 177 Lu-DOTA-IBA therapy had no statistically significant effect on bone marrow hematopoietic function, liver function, and kidney function at any follow-up visit. Bone pain palliation was achieved in 82% (14/17) of patients. The 8-week follow-up 68 Ga-DOTA-IBA PET/CT demonstrated partial response in 3 patients, disease progression in 1 patient, and stable disease in 14 patients.
68 Ga/ 177 Lu-DOTA-IBA provides a set of potential theranostic radiopharmaceuticals and may have a good prospect for the management of bone metastasis.
我们设计并合成了一种新型的治疗性双膦酸盐放射性药物( 68 Ga-或 177 Lu 标记的 DOTA-伊班膦酸[ 68 Ga/ 177 Lu-DOTA-IBA]),用于骨转移。在这项研究中,我们基于 68 Ga-和 177 Lu-DOTA-IBA 图像、血液样本和剂量学分析,评估了 68 Ga/ 177 Lu-DOTA-IBA 作为骨转移治疗性放射性药物的剂量学、安全性和疗效。
本研究纳入了 18 例常规治疗下发生骨转移且病情进展的恶性肿瘤患者。在 3 天内进行基线 99mTc-MDP SPECT 和 68 Ga-DOTA-IBA PET/CT 比较。患者接受 891.5 ± 301.3 MBq 177 Lu-DOTA-IBA 后,在 14 天内进行连续的 177 Lu-DOTA-IBA SPECT 骨扫描。对主要器官和肿瘤病变进行剂量学评估。通过血液生物标志物评估安全性。采用卡氏功能状态量表(Karnofsky Performance Status,KPS)、疼痛评分和随访 68 Ga-DOTA-IBA PET/CT 评估疗效。
基线 68 Ga-DOTA-IBA PET 对骨转移的检测效果优于 99mTc-MDP SPECT。时间-活性曲线显示 177 Lu-DOTA-IBA 在骨转移部位的摄取和保留较快(24 小时:9.43 ± 2.75%IA;14 天:5.45 ± 2.52%IA)。肝脏、肾脏和红骨髓的时间-活性曲线显示摄取较低,清除较快。骨转移病灶的吸收剂量(6.40 ± 2.13 Gy/GBq)明显高于红骨髓(0.47 ± 0.19 Gy/GBq)、肾脏(0.56 ± 0.19 Gy/GBq)或肝脏(0.28 ± 0.07 Gy/GBq),所有 P 值均<0.001。与基线相比,只有 1 例患者出现新的 1 级白细胞减少症(毒性发生率为 6%)。177 Lu-DOTA-IBA 治疗在任何随访时均未对骨髓造血功能、肝功能和肾功能产生统计学显著影响。82%(14/17)的患者骨痛得到缓解。8 周随访的 68 Ga-DOTA-IBA PET/CT 显示 3 例患者部分缓解,1 例患者疾病进展,14 例患者病情稳定。
68 Ga/ 177 Lu-DOTA-IBA 提供了一套潜在的治疗性放射性药物,可能对骨转移的治疗具有良好的前景。