TY - JOUR
T1 - Which Factors Predict Overall Survival in Patients With Metastatic Castration-Resistant Prostate Cancer Treated With Abiraterone Acetate Post-Docetaxel?
AU - Van Praet, Charles
AU - Rottey, Sylvie
AU - Van Hende, Fransien
AU - Pelgrims, Gino
AU - Demey, Wim
AU - Van Aelst, Filip
AU - Wynendaele, Wim
AU - Gil, Thierry
AU - Schatteman, Peter
AU - Filleul, Bertrand
AU - Schallier, Denis
AU - Machiels, Jean-Pascal
AU - Schrijvers, Dirk
AU - Everaert, Els
AU - D'Hondt, Lionel
AU - Werbrouck, Patrick
AU - Vermeij, Joanna
AU - Mebis, Jeroen
AU - Clausse, Marylene
AU - Rasschaert, Marika
AU - Van Erps, Joanna
AU - Verheezen, Jolanda
AU - Van Haverbeke, Jan
AU - Goeminne, Jean-Charles
AU - Lumen, Nicolaas
N1 - Copyright © 2017 Elsevier Inc. All rights reserved.
PY - 2017/8
Y1 - 2017/8
N2 - BACKGROUND: Abiraterone acetate (AA) increases overall survival (OS) in patients with metastatic castration-resistant prostate cancer (mCRPC) previously treated with docetaxel. However, survival time varies substantially between individuals. Our goal was to identify prognostic factors that better estimate OS.MATERIALS AND METHODS: This is a retrospective multicentric analysis of 368 patients with mCRPC starting AA with prednisone after docetaxel. Cox proportional hazards statistics were applied. A multivariate model was constructed based on significant univariate predictors by using a manual stepwise forward and backward selection strategy. Model performance was determined by using receiver operating characteristic (ROC) curves.RESULTS: Univariate analysis identified 20 significant OS predictors. A multivariate model was constructed, based on 220 patients, incorporating 5 independent risk factors for decreased OS at the time of AA initiation: hemoglobin < 12 g/dL (hazard ratio [HR] 2.02), > 10 metastases (HR 1.80), ECOG performance status ≥ 2 (HR 1.88), radiographic progression (HR 1.50), and time since diagnosis < 90 months (HR 1.66, all P < .05). Patients were stratified into 3 groups: good (0-2 risk factors, median OS 22.6 months), intermediate (3 risk factors, median OS 13.9 months), and poor prognosis (4-5 risk factors, median OS 6.2 months). The area under the ROC curve based on the event "death by the time of median OS (13.3 months)" was 0.736 (95% confidence interval 0.670-0.803).CONCLUSION: We identified 5 readily available risk factors independently associated with decreased OS. The resulting model may be used for patient counseling in daily clinical practice, as well as patient stratification in clinical trials.
AB - BACKGROUND: Abiraterone acetate (AA) increases overall survival (OS) in patients with metastatic castration-resistant prostate cancer (mCRPC) previously treated with docetaxel. However, survival time varies substantially between individuals. Our goal was to identify prognostic factors that better estimate OS.MATERIALS AND METHODS: This is a retrospective multicentric analysis of 368 patients with mCRPC starting AA with prednisone after docetaxel. Cox proportional hazards statistics were applied. A multivariate model was constructed based on significant univariate predictors by using a manual stepwise forward and backward selection strategy. Model performance was determined by using receiver operating characteristic (ROC) curves.RESULTS: Univariate analysis identified 20 significant OS predictors. A multivariate model was constructed, based on 220 patients, incorporating 5 independent risk factors for decreased OS at the time of AA initiation: hemoglobin < 12 g/dL (hazard ratio [HR] 2.02), > 10 metastases (HR 1.80), ECOG performance status ≥ 2 (HR 1.88), radiographic progression (HR 1.50), and time since diagnosis < 90 months (HR 1.66, all P < .05). Patients were stratified into 3 groups: good (0-2 risk factors, median OS 22.6 months), intermediate (3 risk factors, median OS 13.9 months), and poor prognosis (4-5 risk factors, median OS 6.2 months). The area under the ROC curve based on the event "death by the time of median OS (13.3 months)" was 0.736 (95% confidence interval 0.670-0.803).CONCLUSION: We identified 5 readily available risk factors independently associated with decreased OS. The resulting model may be used for patient counseling in daily clinical practice, as well as patient stratification in clinical trials.
KW - Chemotherapy
KW - Prognosis
KW - Prostatic neoplasms
KW - Steroids
KW - Survival
KW - Prednisone/therapeutic use
KW - Humans
KW - Docetaxel
KW - Proportional Hazards Models
KW - Male
KW - Treatment Outcome
KW - Taxoids/therapeutic use
KW - Survival Analysis
KW - Abiraterone Acetate/therapeutic use
KW - ROC Curve
KW - Aged
KW - Retrospective Studies
KW - Prostatic Neoplasms, Castration-Resistant/drug therapy
UR - http://www.scopus.com/inward/record.url?scp=85014057026&partnerID=8YFLogxK
U2 - 10.1016/j.clgc.2017.01.019
DO - 10.1016/j.clgc.2017.01.019
M3 - Article
C2 - 28258960
VL - 15
SP - 502
EP - 508
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
SN - 1558-7673
IS - 4
ER -