Liu Richard F, Juwara Lamin, Ferrario Cristiano, Probst Stephan M
Department of Nuclear Medicine, Jewish General Hospital, 3755 Chem. de la Côte-Sainte-Catherine, Montreal, QC H3T 1E2 Canada.
Quantitative Life Sciences, McGill University, Montreal, QC Canada.
Nucl Med Mol Imaging. 2022 Oct;56(5):228-235. doi: 10.1007/s13139-022-00760-8. Epub 2022 Jul 27.
Radium-223 has been demonstrated in clinical trials to improve survival in castration-resistant prostate cancer (CRPC) patients with bone metastases. However, its performance in routine use remains to be fully characterized. This study aims to describe patient outcomes in the real world as well as identify factors associated with completion of the 6-dose regimen and alkaline phosphatase (ALP) response.
Thirty-six patients who received at least one dose of radium-223 at the Jewish General Hospital in Montréal, Canada, were analysed in a retrospective manner. Using logistic regression, the primary analysis aimed to identify factors associated with treatment completion, and the secondary analysis aimed to identify factors associated with ALP response.
Twenty-one out of 36 patients received all 6 doses of radium-223. Fifteen patients had an ALP response, defined as a 30% decrease in ALP from baseline values. On primary analysis, baseline ALP > 120 U/L and prostate-specific antigen (PSA) > 50 μg/L were significantly associated with lower therapy completion rates (OR = 0.10, = 0.004; OR = 0.18, = 0.022 respectively). On adjustment for confounders, only ALP remained significant (OR = 0.14, = 0.021). Clinical disease progression was the most common reason for treatment non-completion, and it was also associated with elevated baseline ALP (OR = 6.00, = 0.044). On secondary analysis, previous chemotherapy for CRPC was a negative predictor of ALP response (OR = 0.15, = 0.034).
Elevated baseline ALP and PSA were associated with a lower rate of radium-223 regimen completion; receiving chemotherapy for CRPC prior to radium-223 was associated with a lower rate of ALP response.
The online version contains supplementary material available at 10.1007/s13139-022-00760-8.
在临床试验中已证实,镭 - 223可提高伴有骨转移的去势抵抗性前列腺癌(CRPC)患者的生存率。然而,其在常规使用中的表现仍有待全面描述。本研究旨在描述现实世界中的患者结局,并确定与完成6剂治疗方案及碱性磷酸酶(ALP)反应相关的因素。
对在加拿大蒙特利尔犹太总医院接受至少一剂镭 - 223治疗的36例患者进行回顾性分析。采用逻辑回归分析,主要分析旨在确定与治疗完成相关的因素,次要分析旨在确定与ALP反应相关的因素。
36例患者中有21例接受了全部6剂镭 - 223治疗。15例患者出现ALP反应,定义为ALP较基线值降低30%。在主要分析中,基线ALP>120 U/L和前列腺特异性抗原(PSA)>50 μg/L与较低的治疗完成率显著相关(OR分别为0.10,P = 0.004;OR为0.18,P = 0.022)。在对混杂因素进行校正后,只有ALP仍具有显著性(OR = 0.14,P = 0.021)。临床疾病进展是治疗未完成的最常见原因,且它也与基线ALP升高相关(OR = 6.00,P = 0.044)。在次要分析中,既往针对CRPC的化疗是ALP反应的负性预测因素(OR = 0.15,P = 0.034)。
基线ALP和PSA升高与镭 - 223治疗方案的较低完成率相关;在镭 - 223治疗前接受针对CRPC的化疗与较低的ALP反应率相关。
在线版本包含可在10.1007/s13139 - 022 - 00760 - 8获取的补充材料。