TY - JOUR
T1 - Association of biomarkers with serious cardiac adverse events during abiraterone acetate treatment in castration resistant prostate cancer
AU - Campora, Sara
AU - Campazzi, Eleonora
AU - Zanardi, Silvia
AU - Puntoni, Matteo
AU - Piccininno, Marco
AU - Piccardo, Arnoldo
AU - Naseri, Mehrdad Shoushtari Zadeh
AU - Defferrari, Carlotta
AU - Provinciali, Nicoletta
AU - Petrera, Marilena
AU - Marra, Domenico
AU - Biscaldi, Ennio
AU - Antonucci, Gian Carlo
AU - Ricci, Damiano
AU - Clavarezza, Matteo
AU - Gennari, Alessandra
AU - Gozza, Alberto
AU - D’Amico, Mauro
AU - Mori, Marco
AU - DeCensi, Andrea
N1 - Publisher Copyright:
© 2016 The Authors.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - BACKGROUND: Abiraterone acetate is an effective drug for castration-resistant prostate cancer, but cardiac serious adverse events (SAEs) may occur. We studied their association with N-terminal pro-brain natriuretic peptide (NT-proBNP) and troponin T (TnT) during abiraterone therapy. PATIENTS AND METHODS: In a single institution, 17 patients were treated with abiraterone acetate 1 g daily with concomitant prednisone and then switched to dexametasone plus canrenone. Blood samples for PSA, NT-proBNP, and TnT were obtained at baseline and after 1, 3, and 6 months. RESULTS: Five patients (29.4%) experienced G3 to 4 cardiac SAEs after a median of 13 weeks (range, 9-32), including pulmonary edema, heart failure, acute coronary syndrome, sinus bradycardia with syncope, and pulmonary edema. At baseline, 4 weeks, and 3 months, median NT-proBNP and TnT levels were higher in patients with subsequent cardiac SAEs (P=.03 and P=.04 for NT-proBNP and TnT at 3 months, respectively). After switching to dexametasone and introducing canrenone, no additional cardiac SAEs were noted. Overall response rate was 67%. CONCLUSIONS: Our study suggests a higher than expected risk of cardiac SAEs during abiraterone treatment which may well be due to the small sample size and the unrestricted entry criteria. However, baseline and frequent NT-proBNP and TnT monitoring predicted a higher risk for cardiac SAE. Larger studies should confirm our findings.
AB - BACKGROUND: Abiraterone acetate is an effective drug for castration-resistant prostate cancer, but cardiac serious adverse events (SAEs) may occur. We studied their association with N-terminal pro-brain natriuretic peptide (NT-proBNP) and troponin T (TnT) during abiraterone therapy. PATIENTS AND METHODS: In a single institution, 17 patients were treated with abiraterone acetate 1 g daily with concomitant prednisone and then switched to dexametasone plus canrenone. Blood samples for PSA, NT-proBNP, and TnT were obtained at baseline and after 1, 3, and 6 months. RESULTS: Five patients (29.4%) experienced G3 to 4 cardiac SAEs after a median of 13 weeks (range, 9-32), including pulmonary edema, heart failure, acute coronary syndrome, sinus bradycardia with syncope, and pulmonary edema. At baseline, 4 weeks, and 3 months, median NT-proBNP and TnT levels were higher in patients with subsequent cardiac SAEs (P=.03 and P=.04 for NT-proBNP and TnT at 3 months, respectively). After switching to dexametasone and introducing canrenone, no additional cardiac SAEs were noted. Overall response rate was 67%. CONCLUSIONS: Our study suggests a higher than expected risk of cardiac SAEs during abiraterone treatment which may well be due to the small sample size and the unrestricted entry criteria. However, baseline and frequent NT-proBNP and TnT monitoring predicted a higher risk for cardiac SAE. Larger studies should confirm our findings.
UR - http://www.scopus.com/inward/record.url?scp=85001000702&partnerID=8YFLogxK
U2 - 10.1016/j.tranon.2016.08.001
DO - 10.1016/j.tranon.2016.08.001
M3 - Review article
SN - 1936-5233
VL - 9
SP - 600
EP - 605
JO - Translational Oncology
JF - Translational Oncology
IS - 6
ER -