Clinical Outcome Patterns of Use of Radium-223 in Patients with Metastatic Castration-Resistant Prostate Cancer

<b>Introduction:</b> Radium-223 dichloride (radium-223) is a bone-targeting radioisotope therapy that aids in the survival of patients with metastatic castration-resistant prostate cancer (mCRPC) to bones. This study aimed to describe the clinical characteristics and outcomes of patients with mCRPC treated with radium-223 in a real-world setting. <b>Methods:</b> This was a retrospective study of patients with mCRPC treated with radium-223 between 2016 and 2020 at the London Health Sciences Centre in London, Canada. The baseline characteristics between the patients receiving 1-3 and 4-6 treatment cycles were compared using a two-sample t-test and Chi-square test. ANOVA was used to determine if there was a difference in each diagnostic variable per treatment cycle. Kaplan-Meier curves were generated to estimate progression-free survival (PFS) and overall survival in the patients treated with different numbers of cycles. <b>Results:</b> Fifty eligible patients were identified. The median age was 71 years (IQR: 66-76). Most patients (62%) received radium-223 beyond the third-line treatment. The mean number of radium-223 treatments was four. While 60% of the patients received 4-6 injections, 40% received 1-3 injections. Fifty-eight percent (58%) of the patients demonstrated a clinical benefit, with the remainder expressing either disease progression (28%) or stable disease (10%). The patients treated with 4-6 cycles had a delay to disease progression compared to those given 1-3 cycles of radium-223 (F<sub>5,35</sub> = 10.52, <i>p</i> < 0.001). A higher alkaline phosphatase level prior to treatment was associated with a longer PFS (z<sub>33</sub> = 2.362, <i>p</i> = 0.018). Treatment-related hospitalization for skeletal-related events was noted in 8% of the patients, and 14% required treatment discontinuation due to hematologic toxicity. <b>Conclusions:</b> This study confirms the safety of radium-223 in patients with mCRPC in a real-world setting. The radium-223 treatment was associated with a clinical benefit in the majority of the patients, particularly in those with higher pre-treatment serum alkaline phosphatase levels. Further studies to identify the predictive biomarkers are warranted to better guide the contemporary use of radium-223.

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Journal
Current Oncology
Published
2024-10-22
DOI
https://doi.org/10.3390/curroncol31110480
Primary Topic
Prostate Cancer Treatment and Research
Type
article
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article

Clinical Outcome Patterns of Use of Radium-223 in Patients with Metastatic Castration-Resistant Prostate Cancer

David Laidley, Scott Ernst, Jasna Deluce, Eric Winquist et al.
Current Oncology
Prostate Cancer Treatment and Research
article

Clinical Outcome Patterns of Use of Radium-223 in Patients with Metastatic Castration-Resistant Prostate Cancer

David Laidley, Scott Ernst, Jasna Deluce, Eric Winquist, Emma Churchman, Morgan Black, Colin R. MacKenzie, Matthew Parezanovic, Ricardo Fernandes, Kylea Potvin
article en

Abstract

<b>Introduction:</b> Radium-223 dichloride (radium-223) is a bone-targeting radioisotope therapy that aids in the survival of patients with metastatic castration-resistant prostate cancer (mCRPC) to bones. This study aimed to describe the clinical characteristics and outcomes of patients with mCRPC treated with radium-223 in a real-world setting. <b>Methods:</b> This was a retrospective study of patients with mCRPC treated with radium-223 between 2016 and 2020 at the London Health Sciences Centre in London, Canada. The baseline characteristics between the patients receiving 1-3 and 4-6 treatment cycles were compared using a two-sample t-test and Chi-square test. ANOVA was used to determine if there was a difference in each diagnostic variable per treatment cycle. Kaplan-Meier curves were generated to estimate progression-free survival (PFS) and overall survival in the patients treated with different numbers of cycles. <b>Results:</b> Fifty eligible patients were identified. The median age was 71 years (IQR: 66-76). Most patients (62%) received radium-223 beyond the third-line treatment. The mean number of radium-223 treatments was four. While 60% of the patients received 4-6 injections, 40% received 1-3 injections. Fifty-eight percent (58%) of the patients demonstrated a clinical benefit, with the remainder expressing either disease progression (28%) or stable disease (10%). The patients treated with 4-6 cycles had a delay to disease progression compared to those given 1-3 cycles of radium-223 (F<sub>5,35</sub> = 10.52, <i>p</i> < 0.001). A higher alkaline phosphatase level prior to treatment was associated with a longer PFS (z<sub>33</sub> = 2.362, <i>p</i> = 0.018). Treatment-related hospitalization for skeletal-related events was noted in 8% of the patients, and 14% required treatment discontinuation due to hematologic toxicity. <b>Conclusions:</b> This study confirms the safety of radium-223 in patients with mCRPC in a real-world setting. The radium-223 treatment was associated with a clinical benefit in the majority of the patients, particularly in those with higher pre-treatment serum alkaline phosphatase levels. Further studies to identify the predictive biomarkers are warranted to better guide the contemporary use of radium-223.

Current OncologyVol. 31(11)
Western University (CA), London Health Sciences Centre (CA), Abbotsford Veterinary Clinic (CA), Victoria Hospital (CA)
Good health and well-being
Openalex Percentile: Top 66%
Prostate Cancer Treatment and Research
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