鐳223用於轉移性賀爾蒙抗性攝護腺癌之治療劑量與臨床結果比較:
單一醫學中心治療經驗
蔡勝閔1、劉建良2,蘇家震1、李高漢1、謝昆霖1、黃冠華1
台南永康奇美醫學中心 外科部 泌尿科1,泌尿腫瘤科2
Comparison of Dosage and Clinical Outcome of Ra-223 in mCRPC: Real World Data from Single Center
Sheng-Min Tsai1、Chien-Liang Liu1、Chia-Cheng Su1、Kau-Han Li1、Kun-Lin Hsieh1、Steven K. Huang1
1Division of Urology, Department of Surgery, Chi Mei Medical Center, Tainan, Taiwan;
2Division of Uro-Oncology, Department of Surgery, Chi Mei Medical Center, Tainan, Taiwan;
Purpose:
Chemotherapy, novel hormonal agents and radium-223 have shown robust evidence of survival in patients with bone metastatic castration-resistant prostate cancer (mCRPC). Besides, radium-223 has better health related quality of life (HRQoL) benefit in symptomatic patients. However, expensive medical cost of radium-223 is a major concern for patients. Radium-223 has been approved in Taiwan's National Health Insurance System since 2019 and the therapy of Radium-223 became affordable. Our aim is to review the patients underwent Radium-223 in our institution since 2019.
Material and Methods:
We retrospectively reviewed patients with prostate cancer and received treatment of Ra-223 at the Chi Mei Medical Center between 2019/1 and 2022/9. We excluded patients with mHSPC and visceral metastasis. In total, 28 patients were enrolled and categorized by dosage of Ra-223. The outcomes of interest included overall survival (OS), survival interval since Ra- 223 use and time to opioid use
Results:
The patients were divided into high dosage group (5 or 6 dosage) and incomplete treatment group (less then 4 dosage). The high dosage group has better OS (median 34.5 vs 12.5months) and superior survival interval since Ra-223 use (median 13 vs 4months). On comparison of time to opioid use, patients with 6 dosages have more benefit then 5 dosage and incomplete treatment group (median 13 vs 6 vs 3.5months).
Conclusion:
Benefit of survival outcome, time to opioid use and survival interval since Ra-223 use is strongly related with the dosage. The trend is compatible with the ALSYMPCA trial in 2013.