The safety of radium-223 combined with new-generation hormonal agents in bone metastatic castration-resistant prostate cancer: a systematic review and network meta-analysis.
Ming-Hao WangJin-Dong DaiXing-Ming ZhangJin-Ge ZhaoGuang-Xi SunYu-Hao ZengHong ZengNan-Wei XuHao ZengPeng-Fei ShenPublished in: Asian journal of andrology (2023)
Patients with bone metastatic castration-resistant prostate cancer (mCRPC) might benefit from radium-223 ( 223 Ra) combined with new-generation hormonal agents (NHAs) in terms of survival and quality of life (QoL). However, the safety of combination therapies remains unclear. Therefore, we aimed to perform a network meta-analysis by reviewing the literature about the combination of 223 Ra with abiraterone acetate plus prednisone (AAP) or enzalutamide and to evaluate the safety of combination therapy in bone mCRPC patients. Ultimately, ten studies (2835 patients) were selected, including four randomized controlled trials (RCTs), five retrospective cohort studies, and one single-arm study. Overall, there was no difference in the incidence of fracture between the 223 Ra+NHA combination group and the 223 Ra monotherapy group (odds ratio [OR]: 1.46, 95% confidence interval [CI]: 0.91-2.34, P = 0.66), but the incidences in both the 223 Ra+NHA combination group (OR: 3.22, 95% CI: 2.24-4.63, P < 0.01) and the 223 Ra monotherapy group (OR: 2.24, 95% CI: 1.23-4.08, P < 0.01) were higher than that in the NHA monotherapy group. However, in the meta-analysis involving only RCTs, there was no difference between the 223 Ra monotherapy group and the NHA monotherapy group (OR: 1.14, 95% CI: 0.22-5.95, P = 0.88), while the difference between the 223 Ra+NHA combination group and the NHA monotherapy group remained significant (OR: 3.22, 95% CI: 2.24-4.63, P < 0.01). Symptomatic skeletal events (SSEs), SSE-free survival (SSE-FS), all grades of common adverse events (AEs), and ≥grade 3 AEs among all groups did not show any significant difference. Our results indicate that the combination of 223 Ra with NHAs was well tolerated in bone mCRPC patients compared to 223 Ra monotherapy, even though the incidence of fracture was higher in patients who received 223 Ra than that among those who received NHA monotherapy. More evidence is needed to explore the safety and efficiency of 223 Ra combination therapies.
Keyphrases
- combination therapy
- rheumatoid arthritis
- disease activity
- end stage renal disease
- ankylosing spondylitis
- systematic review
- newly diagnosed
- open label
- chronic kidney disease
- ejection fraction
- squamous cell carcinoma
- randomized controlled trial
- small cell lung cancer
- bone mineral density
- prostate cancer
- prognostic factors
- free survival
- risk factors
- metabolic syndrome
- systemic lupus erythematosus
- clinical trial
- skeletal muscle
- adipose tissue
- insulin resistance
- double blind