Risk of skeletal related events among elderly prostate cancer patients by site of metastasis at diagnosis

被引:23
作者
Hussain, Arif [1 ,2 ]
Aly, Abdalla [3 ]
Mullins, C. Daniel [4 ]
Qian, Yi [5 ]
Arellano, Jorge [5 ]
Onukwugha, Eberechukwu [4 ]
机构
[1] Univ Maryland, Sch Med, Marlene & Stewart Greenebaum Canc Ctr Baltimore, Baltimore, MD 21201 USA
[2] Vet Affairs Med Ctr, Baltimore, MD USA
[3] Pharmerit Int, Bethesda, MD USA
[4] Univ Maryland, Sch Pharm, Dept Pharmaceut Hlth Serv Res, Baltimore, MD 21201 USA
[5] Amgen Inc, Thousand Oaks, CA 91320 USA
来源
CANCER MEDICINE | 2016年 / 5卷 / 11期
关键词
Prostate cancer; site of metastasis; skeletal-related events; ANDROGEN DEPRIVATION THERAPY; BONE METASTASES; ZOLEDRONIC ACID; DENOSUMAB; SURVIVAL; QUALITY; IMPACT; MEN;
D O I
10.1002/cam4.914
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study was to estimate the risk of developing skeletal-related events (SREs) based on site of metastasis at diagnosis and identify other predictors of developing SREs among metastatic prostate cancer patients. We conducted a retrospective cohort study using linked SEER (Surveillance, Epidemiology, and End Results) and Medicare data and identified men over the age of 65 with incident metastatic prostate cancer diagnosed during 2005-2009. SREs included radiation (RAD), pathological fractures (PF), bone surgery (BS), and spinal cord compression (SCC). The association between site of metastasis at diagnosis and SRE was examined using a Cox proportional hazards model that accounts for death as a competing risk. Among 4404 men (median age: 79 years) with incident metastatic prostate cancer, 44% experienced SREs at a median of 9.6 months post diagnosis. Compared to bone metastasis only, our model showed that patients were significantly less likely to develop SREs if they had LN-only metastasis at diagnosis (Sub-Hazard Ratio [SHR] 0.56; 95% Confidence Interval [CI]: 0.43-0.72) or unknown site of metastasis (SHR: 0.79; CI: 0.64-0.97). Other predictors of reduced SRE risk were age 80+ years (SHR: 0.83; CI: 0.75-0.91), non-Hispanic Black (SHR: 0.77; CI: 0.65-0.90), or being diagnosed in year 2009 (SHR: 0.85; CI: 0.72-0.99). Patients were significantly more likely to develop SREs if they received androgen deprivation therapy (SHR: 1.73; CI: 1.48-2.02) or had Gleason score 8-10 disease (SHR: 0.79; CI: 0.64-0.97). Compared to patients who present with bone metastasis only at diagnosis, patients presenting with other metastatic sites have similar risk of developing SREs, with the exception of those presenting with lymph node only metastasis who have a significantly reduced risk of SREs.
引用
收藏
页码:3300 / 3309
页数:10
相关论文
共 23 条
  • [1] African Americans, 25-hydroxyvitamin D, and osteoporosis: a paradox
    Aloia, John F.
    [J]. AMERICAN JOURNAL OF CLINICAL NUTRITION, 2008, 88 (02) : 545S - 550S
  • [2] Measurement of skeletal related events in SEER-Medicare: a comparison of claims-based methods
    Aly, Abdalla
    Onukwugha, Eberechukwu
    Woods, Corinne
    Mullins, C. Daniel
    Kwok, Young
    Qian, Yi
    Arellano, Jorge
    Balakumaran, Arun
    Hussain, Arif
    [J]. BMC MEDICAL RESEARCH METHODOLOGY, 2015, 15
  • [3] [Anonymous], 2015, SEER MEDICARE BRIEF
  • [4] Timing of androgen deprivation therapy use and fracture risk among elderly men with prostate cancer in the United States
    Beebe-Dimmer, Jennifer L.
    Cetin, Karynsa
    Shahinian, Vahakn
    Morgenstern, Hal
    Yee, Cecilia
    Schwartz, Kendra L.
    Acquavella, John
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2012, 21 (01) : 70 - 78
  • [5] Trends and Racial Differences in the Use of Androgen Deprivation Therapy for Metastatic Prostate Cancer
    Carson, April P.
    Howard, Daniel L.
    Carpenter, William R.
    Taylor, Yhenneko J.
    Peacock, Sharon
    Schenck, Anna P.
    Godley, Paul A.
    [J]. JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2010, 39 (05) : 872 - 881
  • [6] US Food and Drug Administration Approval of Drugs for the Treatment of Prostate Cancer: A New Era Has Begun
    D'Amico, Anthony V.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (04) : 362 - 364
  • [7] Metastatic castration-resistant prostate cancer: changing landscape with cabazitaxel
    Fernandez, Ovidio
    Afonso, Javier
    Vazquez, Sergio
    Campos, Begona
    Lazaro, Matin
    Leon, Luis
    Anton Aparicio, Luis M.
    [J]. ANTI-CANCER DRUGS, 2014, 25 (03) : 237 - 243
  • [8] Denosumab versus zoledronic acid for treatment of bone metastases in men with castration-resistant prostate cancer: a randomised, double-blind study
    Fizazi, Karim
    Carducci, Michael
    Smith, Matthew
    Damiao, Ronaldo
    Brown, Janet
    Karsh, Lawrence
    Milecki, Piotr
    Shore, Neal
    Rader, Michael
    Wang, Huei
    Jiang, Qi
    Tadros, Sylvia
    Dansey, Roger
    Goessl, Carsten
    [J]. LANCET, 2011, 377 (9768) : 813 - 822
  • [9] Systematic review of the clinical effectiveness and cost-effectiveness, and economic evaluation, of denosumab for the treatment of bone metastases from solid tumours
    Ford, J.
    Cummins, E.
    Sharma, P.
    Elders, A.
    Stewart, F.
    Johnston, R.
    Royle, P.
    Jones, R.
    Mulatero, C.
    Todd, R.
    Mowatt, G.
    [J]. HEALTH TECHNOLOGY ASSESSMENT, 2013, 17 (29) : 1 - +
  • [10] Doubly Robust Estimation of Causal Effects
    Funk, Michele Jonsson
    Westreich, Daniel
    Wiesen, Chris
    Stuermer, Til
    Brookhart, M. Alan
    Davidian, Marie
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2011, 173 (07) : 761 - 767