Factors Associated With Survival Following Radium-223 Treatment for Metastatic Castration-resistant Prostate Cancer

被引:50
|
作者
Wong, William W. [1 ]
Anderson, Eric M. [1 ]
Mohammadi, Homan [1 ]
Daniels, Thomas B. [1 ]
Schild, Steve E. [1 ]
Keole, Sameer R. [1 ]
Choo, C. Richard [2 ]
Tzou, Katherine S. [3 ]
Bryce, Alan H. [4 ]
Ho, Thai H. [4 ]
Quevedo, Fernando J. [5 ]
Vora, Sujay A. [1 ]
机构
[1] Mayo Clin Arizona, Dept Radiat Oncol, 5777 E Mayo Blvd, Phoenix, AZ 85054 USA
[2] Mayo Clin Rochester, Dept Radiat Oncol, Rochester, MN USA
[3] Mayo Clin Florida, Dept Radiat Oncol, Jacksonville, FL USA
[4] Mayo Clin Arizona, Div Hematol Oncol, Phoenix, AZ 85054 USA
[5] Mayo Clin Rochester, Div Oncol, Rochester, MN USA
关键词
Alpha-emitter; Bone metastasis; Bone-targeting agent; Palliative radiation; Radiopharmaceutical; DOCETAXEL; MITOXANTRONE; PREDNISONE; DICHLORIDE; ALSYMPCA; THERAPY; RA-223;
D O I
10.1016/j.clgc.2017.04.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The outcomes of 64 patients with metastatic castration-resistant prostate cancer after treatment with radium223 were analyzed. Four factors were identified to be associated with survival in multivariate analysis. Future studies to evaluate earlier use of this radiopharmaceutical in newly diagnosed metastatic prostate cancer when the disease is sensitive to androgen deprivation therapy would be warranted. Background: Radium-223 (Ra-223) improves survival in patients with metastatic castration-resistant prostate cancer (mCRPC). This retrospective analysis was performed to better understand its efficacy in routine clinical practice and identify factors associated with survival. Materials and Methods: Sixty-four patients with mCRPC who received Ra-223 between 2013 and 2015 were the basis of this retrospective study. Clinical outcomes and patient characteristics were obtained. Potential prognostic factors for survival were evaluated by univariate analysis using the log-rank test and multivariate analysis using the Cox proportional hazard method. Results: The median survival was 12.9 months. Twenty-one patients (33%) developed a skeletal event, and the median time to the first skeletal event was 4.4 months. In univariate analysis, factors significantly associated with survival included: no prior chemotherapy, <= 5 bone metastases, baseline prostate-specific antigen (PSA) <= 36 ng/mL, baseline alkaline phosphatase (ALP) < 115 U/L, baseline hemoglobin > 12 g/dL, ALP response after Ra-223 treatment, PSA decrease during Ra-223 treatment, and absence of > 25% PSA increase during Ra-223 treatment. In multivariate analysis, 4 factors remained significant: no prior chemotherapy, <= 5 bone metastases, baseline ALP < 115 U/L, and ALP response after Ra-223 treatment. Conclusion: When Ra-223 is administered in routine clinical practice, clinical outcomes can be more variable than those reported in the randomized study owing to patient heterogeneity. Four factors were identified to be significantly associated with survival after Ra-223 treatment. These pretreatment factors may be used as stratification factors in future studies to investigate whether Ra-223 would be more effective for patients with newly diagnosed metastatic disease that is sensitive to androgen deprivation therapy. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:E969 / E975
页数:7
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