Nuclear Medicine, University of Brescia and Spedali Civili Brescia, Brescia, Italy.
Nucl Med Commun. 2020 Apr;41(4):300-307. doi: 10.1097/MNM.0000000000001164.
Radium-223 was a treatment approved for patients with metastatic castrate-resistant prostate cancer, symptomatic bone metastases and no-visceral metastases, in progression after at least two prior lines of systemic therapy, or ineligible for any available systemic treatment. The aim of this study was to provide further characterization and sub-selection of patients who would benefit most with Radium-223 treatment.
We retrospectively analysed 38 patients treated with Radium-223 between 2015 and 2018. All patients underwent a baseline visit and a bone scintigraphy. Bone scan, ALP and PSA levels were repeated after third and after the end of therapy. All patients were re-evaluated after 2 months from the end of therapy. Survival curves were plotted according to the Kaplan-Meier method and differences between groups were analysed by using a two-tailed log-rank test.
The response to the treatment in term of change in pain was reduction in 16 patients; no change in 14 and increased in eight. We arbitrarily established a cut-off 10 bone lesions to evaluate the response: patients with less than 10 metastasis had significant differences in PFS (P < 0.001) compared to patients with more than 10, no statistical significance was found considering the OS (P = 0.23) between the two groups. The same results were founded in patients with baseline ALP <220 U/L with a PFS (P < 0.001) and OS (P = 0.027).
The most important finding was the correlation between the number of bone metastasis and ALP with outcome survival and efficacy of Radium-223 treatment.
镭-223 是一种用于治疗转移性去势抵抗性前列腺癌、有症状的骨转移且无内脏转移、至少经过两线系统治疗后进展、或不符合任何现有系统治疗条件的患者的药物。本研究旨在进一步确定最适合镭-223 治疗的患者特征并进行亚组选择。
我们回顾性分析了 2015 年至 2018 年期间接受镭-223 治疗的 38 例患者。所有患者均接受基线访视和骨闪烁显像。在第三次治疗后和治疗结束后,重复进行骨扫描、碱性磷酸酶(ALP)和前列腺特异抗原(PSA)水平检测。所有患者在治疗结束后 2 个月进行重新评估。根据 Kaplan-Meier 法绘制生存曲线,并用双侧对数秩检验分析组间差异。
根据疼痛变化评估治疗反应,16 例患者疼痛缓解,14 例患者疼痛无变化,8 例患者疼痛加重。我们任意设定了一个 10 个骨病变的截断值来评估反应:转移灶少于 10 个的患者与转移灶多于 10 个的患者相比,无进展生存期(PFS)有显著差异(P < 0.001),但两组间总生存期(OS)无统计学差异(P = 0.23)。在基线 ALP <220 U/L 的患者中也发现了同样的结果,他们的 PFS(P < 0.001)和 OS(P = 0.027)有显著差异。
最重要的发现是骨转移和 ALP 的数量与结局生存和镭-223 治疗的疗效相关。