Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center

被引:19
作者
McKay, Rana R. [1 ,2 ]
Silver, Rebecca [1 ]
Bhak, Rachel H. [3 ]
Korves, Caroline [3 ]
Cheng, Mu [3 ]
Appukkuttan, Sreevalsa [4 ]
Simmons, Stacey J. [4 ]
Duh, Mei Sheng [3 ]
Taplin, Mary-Ellen [1 ]
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[3] Anal Grp Inc, Boston, MA 02199 USA
[4] Bayer Healthcare Pharmaceut, Whippany, NJ USA
关键词
ACETATE PLUS PREDNISONE; POST-HOC ANALYSIS; ABIRATERONE ACETATE; DOUBLE-BLIND; CHEMOTHERAPY; SURVIVAL; MEN; ENZALUTAMIDE; DICHLORIDE; DOCETAXEL;
D O I
10.1038/s41391-020-00271-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Guidelines for optimal sequencing of radium-223 and chemotherapy for metastatic castration resistant prostate cancer (mCRPC) do not exist. This study evaluated treatment patterns and overall survival (OS) among patients with mCRPC treated with radium-223 in an academic clinical setting. Methods A retrospective study was conducted of bone metastases-predominant mCRPC patients treated with radium-223. Treatment patterns from 2013 to 2018 were evaluated in patients treated with radium-223 pre- vs. post-chemotherapy. OS was examined using Kaplan-Meier medians and 95% confidence intervals. Results In total, 220 patients were treated with radium-223 (64 pre-chemotherapy, 83 post-chemotherapy, 73 no chemotherapy). Mean radium-223 injections per patient was 5.3 and 4.3 in the pre- vs. post-chemotherapy cohorts, respectively (p < 0.001). The number of chemotherapy cycles was similar for chemotherapy given pre- or post-radium-223. Mean line of mCRPC therapy of radium-223 was 3rd and 5th when given pre- and post-chemotherapy, respectively (p < 0.001). 41.8% patients were treated with radium-223 in combination with another mCRPC therapy, commonly abiraterone acetate (43.5%) or enzalutamide (52.2%). The majority received combination therapy for the duration of radium-223 treatment; 20.7% started another agent after radium-223 initiation; 20.7% initiated radium-223 while on established therapy. Median OS from first mCRPC treatment was 39.4 months (95% CI 33.0, 48.8) for patients with radium-223 pre-chemotherapy vs. 37.4 months (95% CI 32.0, 43.5) post-chemotherapy (and 35.2 months [95% CI 27.9, 43.3] vs. 32.0 months [95% CI 26.9, 36.0] for patients with radium-223 combination vs. monotherapy). Conclusions This retrospective analysis of patients treated with radium-223 demonstrates that administration of radium-223 pre-chemotherapy increased likelihood of completion of radium-223 treatment. Radium-223 given pre- or post-chemotherapy and with or without combination therapy did not result in significant differences in OS. Additional studies are needed to determine the optimal sequencing strategy of mCRPC in the modern era.
引用
收藏
页码:210 / 219
页数:10
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