TY - JOUR
T1 - Predicting Time From Metastasis to Overall Survival in Castration-Resistant Prostate Cancer
T2 - Results From SEARCH
AU - Moreira, Daniel M.
AU - Howard, Lauren E.
AU - Sourbeer, Katharine N.
AU - Amarasekara, Hiruni S.
AU - Chow, Lydia C.
AU - Cockrell, Dillon C.
AU - Pratson, Connor L.
AU - Hanyok, Brian T.
AU - Aronson, William J.
AU - Kane, Christopher J.
AU - Terris, Martha K.
AU - Amling, Christopher L.
AU - Cooperberg, Matthew R.
AU - Freedland, Stephen J.
N1 - Funding Information:
Supported in part by the Department of Veterans Affairs, National Institute of Health (NIH) R01CA100938 (W.J.A.), NIH Specialized Programs of Research Excellence P50 CA92131-01A1 (W.J.A.), the Georgia Cancer Coalition (M.K.T.), NIH K24 CA160653 (S.J.F.), and Janssen.
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - We investigated the predictors of time from metastatic castration-resistant prostate cancer (mCRPC) to all-cause mortality among patients treated at Veteran Affairs hospitals. We found that age, more remote year of mCRPC, greater number of bone metastasis, higher prostate-specific antigen levels, and shorter prostate-specific antigen doubling time at mCRPC diagnosis were associated with shorter overall survival. A nomogram was generated yielding good concordance and calibration. Objective To identify the predictors of time from initial diagnosis of metastatic castration-resistance prostate cancer (mCRPC) to all-cause death within the Shared Equal Access Regional Cancer Hospital cohort. Patients and Methods We performed a retrospective analysis of 205 mCRPC men. Overall survival was estimated and plotted using the Kaplan-Meier method. The uni- and multivariable overall survival predictors were evaluated with the Cox proportional hazards model. A nomogram was generated to predict overall survival at 1, 2, 3, and 5 years after mCRPC. Concordance index and calibration plot were obtained. Results A total of 170 men (83%) died over a median follow-up of 41 months. In univariable analysis, older age, more remote year of mCRPC, nonblack race, greater number of bone metastasis, higher prostate-specific antigen (PSA) levels, shorter PSA doubling time, and faster PSA velocity at mCRPC diagnosis were significantly associated with shorter overall survival (all P < .05). In multivariable analysis, older age, more remote year of mCRPC, greater number of bone metastasis, higher PSA levels, and shorter PSA doubling time at mCRPC diagnosis remained significantly associated with shorter overall survival (all P < .05). On the basis of these variables, a nomogram was generated yielding a concordance index of 0.67 and good calibration. Conclusion The use of clinical parameter such as age, disease burden, and PSA levels and kinetics can be used to estimate overall survival in mCRPC patients.
AB - We investigated the predictors of time from metastatic castration-resistant prostate cancer (mCRPC) to all-cause mortality among patients treated at Veteran Affairs hospitals. We found that age, more remote year of mCRPC, greater number of bone metastasis, higher prostate-specific antigen levels, and shorter prostate-specific antigen doubling time at mCRPC diagnosis were associated with shorter overall survival. A nomogram was generated yielding good concordance and calibration. Objective To identify the predictors of time from initial diagnosis of metastatic castration-resistance prostate cancer (mCRPC) to all-cause death within the Shared Equal Access Regional Cancer Hospital cohort. Patients and Methods We performed a retrospective analysis of 205 mCRPC men. Overall survival was estimated and plotted using the Kaplan-Meier method. The uni- and multivariable overall survival predictors were evaluated with the Cox proportional hazards model. A nomogram was generated to predict overall survival at 1, 2, 3, and 5 years after mCRPC. Concordance index and calibration plot were obtained. Results A total of 170 men (83%) died over a median follow-up of 41 months. In univariable analysis, older age, more remote year of mCRPC, nonblack race, greater number of bone metastasis, higher prostate-specific antigen (PSA) levels, shorter PSA doubling time, and faster PSA velocity at mCRPC diagnosis were significantly associated with shorter overall survival (all P < .05). In multivariable analysis, older age, more remote year of mCRPC, greater number of bone metastasis, higher PSA levels, and shorter PSA doubling time at mCRPC diagnosis remained significantly associated with shorter overall survival (all P < .05). On the basis of these variables, a nomogram was generated yielding a concordance index of 0.67 and good calibration. Conclusion The use of clinical parameter such as age, disease burden, and PSA levels and kinetics can be used to estimate overall survival in mCRPC patients.
KW - Disease-free survival
KW - Mortality
KW - Prostate cancer
KW - Prostate-specific antigen
KW - Prostatectomy
UR - http://www.scopus.com/inward/record.url?scp=85008670838&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85008670838&partnerID=8YFLogxK
U2 - 10.1016/j.clgc.2016.08.018
DO - 10.1016/j.clgc.2016.08.018
M3 - Article
C2 - 27692812
AN - SCOPUS:85008670838
SN - 1558-7673
VL - 15
SP - 60-66.e2
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 1
ER -
