Predictors of survival, healthcare resource utilization, and healthcare costs in veterans with non-metastatic castration-resistant prostate cancer

被引:10
作者
Freedland, Stephen J. [1 ,2 ]
Pilon, Dominic [3 ]
Bhak, Rachel H. [4 ]
Lefebvre, Patrick [4 ]
Li, Sophia [5 ]
Young-Xu, Yinong [6 ,7 ]
机构
[1] Cedars Sinai Med Ctr, Dept Surg, Div Urol, Los Angeles, CA 90048 USA
[2] Durham VA Med Ctr, Urol Sect, Durham, NC USA
[3] Anal Grp Inc, Montreal, PQ, Canada
[4] Anal Grp Inc, Boston, MA USA
[5] Janssen Sci Affairs LLC, Titusville, NJ USA
[6] White River Junct VA Med Ctr, White River Jct, VT USA
[7] Dartmouth Geisel Sch Med, Hanover, NH USA
关键词
Non-metastatic castrate-resistant prostate cancer; Prostate-specific antigen doubling time; Metastasis-free survival; Overall survival; Economic burden; Veteran; METASTASIS-FREE SURVIVAL; BONE-SCAN POSITIVITY; MEN; ANTIGEN; TIME; RISK;
D O I
10.1016/j.urolonc.2020.07.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: The objective of this study was to evaluate the association of prostate-specific antigen doubling time (PSADT) with metastasis-free survival (MFS) and overall survival (OS), and to describe healthcare resource utilization (HRU) and costs among patients with non-metastatic castrate-resistant prostate cancer (nmCRPC) in the Veterans Health Administration setting. Methods and Materials: Patients with nmCRPC were identified from the Veterans Health Administration electronic health record database (1/2007-8/2017). PSADT was categorized as <3 months, 3 to 9 months, 9 to 15 months, >= 15 months, and unknown. MFS and OS were assessed using multivariable Cox proportional hazards regression, including PSADT as a predictor. HRU and costs were described per-patient-per-year (PPPY). Results: Among 12,083 patients in the study, shorter PSADT was associated with shorter MFS and OS (PSADT < 3 months vs. PSADT >= 15 months hazard ratio [HR] [95% confidence interval (CI)] = 0.307 [0.281, 0.335] and 0.371 [0.335, 0.410], respectively). Patients who developed metastasis had a 3-fold higher risk of death compared to those without metastasis (HR [95% CI] = 2.933 [2.763, 3.113]). Mean HRU increased following the onset of nmCRPC and metastatic castrate-resistant prostate cancer (mCRPC); mean inpatient stays more than doubled (0.2 vs. 0.5 and 0.6 vs. 2.8 PPPY, respectively). Similar increases in healthcare costs were observed; pharmacy costs more than tripled following nmCRPC ($2,074 vs. $6,839 PPPY). From nmCRPC to mCRPC, large increases were observed for inpatient costs ($7,257-$ 61,691), emergency room costs ($844-$ 1,958), and pharmacy costs ($4,115-$ 26,279) PPPY. Conclusions: In Veterans with nmCRPC, shorter PSADT was significantly associated with shorter MFS and OS. Onset of nmCRPC and mCRPC was associated with substantial HRU and cost increases. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:930.e13 / 930.e21
页数:9
相关论文
共 25 条
  • [1] Tackling non-metastatic castration-resistant prostate cancer: special considerations in treatment
    Anantharaman, Archana
    Small, Eric J.
    [J]. EXPERT REVIEW OF ANTICANCER THERAPY, 2017, 17 (07) : 625 - 633
  • [2] [Anonymous], 2018, NCCN Clinical Practice Guidelines in Oncology
  • [3] Prostate specific antigen working group guidelines on prostate specific antigen doubling time
    Arlen, Philip M.
    Bianco, Fernando
    Dahut, William L.
    D'Amico, Anthony
    Figg, William D.
    Freedland, Stephen J.
    Gulley, James L.
    Kantoff, Philip W.
    Kattan, Michael W.
    Lee, Andrew
    Regan, Meredith M.
    Sartor, Oliver
    [J]. JOURNAL OF UROLOGY, 2008, 179 (06) : 2181 - 2185
  • [4] Bureau of Labor Statistics (BLS, 2019, MEAS PRIC CHANG CPI
  • [5] Darolutamide in Nonmetastatic, Castration-Resistant Prostate Cancer
    Fizazi, Karim
    Shore, Neal
    Tammela, Teuvo L.
    Ulys, Albertas
    Vjaters, Egils
    Polyakov, Sergey
    Jievaltas, Mindaugas
    Luz, Murilo
    Alekseev, Boris
    Kuss, Iris
    Kappeler, Christian
    Snapir, Amir
    Sarapohja, Toni
    Smith, Matthew R.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2019, 380 (13) : 1235 - 1246
  • [6] Validation of a bone scan positivity risk table in non-metastatic castration-resistant prostate cancer
    Freedland, Stephen J.
    Howard, Lauren E.
    Hanyok, Brian T.
    Kadiyala, Vishnu K.
    Kuang, Jameson Y.
    Whitney, Colette A.
    Wilks, Floyd R.
    Kane, Christopher J.
    Terris, Martha K.
    Amling, Christopher L.
    Cooperberg, Matthew R.
    Aronson, William J.
    Moreira, Daniel M.
    [J]. BJU INTERNATIONAL, 2016, 118 (04) : 570 - 577
  • [7] The impact of time to metastasis on overall survival in patients with prostate cancer
    Frees, Sebastian
    Akamatsu, Shusuke
    Bidnur, Samir
    Khalaf, Daniel
    Chavez-Munoz, Claudia
    Struss, Werner
    Eigl, Bernhard J.
    Gleave, Martin
    Chi, Kim N.
    So, Alan
    [J]. WORLD JOURNAL OF UROLOGY, 2018, 36 (07) : 1039 - 1046
  • [8] Thresholds for PSA doubling time in men with non-metastatic castration-resistant prostate cancer
    Howard, Lauren E.
    Moreira, Daniel M.
    De Hoedt, Amanda
    Aronson, William J.
    Kane, Christopher J.
    Amling, Christopher L.
    Cooperberg, Matthew R.
    Terris, Martha K.
    Freedland, Stephen J.
    [J]. BJU INTERNATIONAL, 2017, 120 (5B) : E80 - E86
  • [9] Enzalutamide in Men with Nonmetastatic, Castration-Resistant Prostate Cancer
    Hussain, Maha
    Fizazi, Karim
    Saad, Fred
    Rathenborg, Per
    Shore, Neal
    Ferreira, Ubirajara
    Ivashchenko, Petro
    Demirhan, Eren
    Modelska, Katharina
    Phung, De
    Krivoshik, Andrew
    Sternberg, Cora N.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2018, 378 (26) : 2465 - 2474
  • [10] Elevated alkaline phosphatase velocity strongly predicts overall survival and the risk of bone metastases in castrate-resistant prostate cancer
    Metwalli, Adam R.
    Rosner, Inger L.
    Cullen, Jennifer
    Chen, Yongmei
    Brand, Timothy
    Brassell, Stephen A.
    Lesperance, James
    Porter, Christopher
    Sterbis, Joseph
    McLeod, David G.
    [J]. UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2014, 32 (06) : 761 - 768