Genitourinary Oncology Service, Institute of Oncology, Meir Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Clinical Physiology, Nuclear Medicine and PET, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Prostate Cancer Prostatic Dis. 2017 Sep;20(3):289-293. doi: 10.1038/pcan.2017.6. Epub 2017 Feb 28.
The imaging response to radium-223 therapy is at present poorly described. We aimed to describe the imaging response to radium-223 treatment.
We retrospectively evaluated the computed tomography (CT) and bone scintigraphy response of metastatic castration-resistant prostate cancer (CRPC) patients treated with radium-223, in eight centers in three countries.
A total of 130 patients were included, the majority (n=84, 65%) received radium-223 post docetaxel. Thirty-four of 99 patients with available data (34%) received concomitant abiraterone or enzalutamide. A total of 54% (n=70) patients completed the planned six injections of radium-223. In patients with available data, a transient increase in bone metastases-related pain was observed in 27% (n=33/124) and an improvement of bone metastases-related pain on treatment with radium-223 was noted in 49% of patients (n=61/124). At 3 and 6 months of treatment with radium-223, bone imaging showed stable disease in 74% (n=84/113) and 94% of patients (n=93/99) with available data, respectively. An increase in the number of bone lesions was documented at 3 months compared with baseline in 26% (n=29/113) and at 6 months compared with 3 months in 6% of patients (n=6/99), respectively. Radiological extraskeletal disease progression occurred in 46% of patients (n=57/124) with available CT data at 3 and/or 6 months.
Progression of bone metastases during radium-223 therapy is uncommon. A bone flare (pain and/or radiological) may be noted during the first 3 months, and should not be confused with progression. Imaging by CT scan should be considered after three and six doses of radium-223 to rule out extraskeletal disease progression.
镭-223 治疗的影像学反应目前描述得很差。我们旨在描述镭-223 治疗的影像学反应。
我们回顾性评估了在三个国家的八个中心接受镭-223 治疗的转移性去势抵抗性前列腺癌(CRPC)患者的计算机断层扫描(CT)和骨闪烁扫描反应。
共纳入 130 例患者,其中大多数(n=84,65%)在接受多西他赛后接受镭-223 治疗。99 例有可用数据的患者中,有 34 例(34%)同时接受阿比特龙或恩杂鲁胺治疗。共有 54%(n=70)的患者完成了计划的 6 次镭-223 注射。在有可用数据的患者中,27%(n=33/124)观察到骨转移相关疼痛短暂增加,49%的患者(n=61/124)在接受镭-223 治疗后骨转移相关疼痛得到改善。在镭-223 治疗 3 个月和 6 个月时,骨影像学显示有 74%(n=84/113)和 94%的患者(n=93/99)分别存在稳定疾病。与基线相比,在 3 个月时有 26%(n=29/113)的患者和在 6 个月时有 6%的患者(n=6/99)记录到骨病变数量增加。在有可用 CT 数据的 3 个月和/或 6 个月时,46%的患者(n=57/124)发生骨骼外疾病进展。
镭-223 治疗期间骨转移进展并不常见。在最初的 3 个月内可能会出现骨 flare(疼痛和/或影像学),不应与进展混淆。在接受镭-223 治疗 3 次和 6 次后,应考虑进行 CT 扫描成像以排除骨骼外疾病进展。