Back to Search
Start Over
Corticosteroid switch in heavily pre-treated castration-resistant prostate cancer patients progressed on abiraterone acetate plus prednisone.
- Source :
-
Investigational new drugs [Invest New Drugs] 2018 Dec; Vol. 36 (6), pp. 1110-1115. Date of Electronic Publication: 2018 Oct 22. - Publication Year :
- 2018
-
Abstract
- The aim of this retrospective study is to evaluate the activity and safety of a steroidal switch from prednisone to dexamethasone in patients with advanced, heavily pre-treated, castration-resistant prostate cancer (CRPC) who progressed on abiraterone acetate. Treatment consisted of oral daily abiraterone plus dexamethasone (0.5 mg once daily) administered until disease progression or unacceptable toxicity. Thirty-six patients were evaluated: all men underwent a prior treatment with enzalutamide. A PSA decrease ≥50% was observed in 11% of patients; median progression-free survival was 10.8 weeks (95% CI: 9.2-16), and median survival was 17.6 weeks (95% CI: 15.8-28.8). Better efficacy and survival were observed in the subgroup of patients treated with abiraterone acetate prior for a period >3 months; treatment was well tolerated, and no grade 3-4 toxicities were observed. Our findings did not suggest the use of steroid switch in all CRPC who were heavily pre-treated. However, the switch could be an option for patients who responded well to prior abiraterone acetate treatment.
- Subjects :
- Abiraterone Acetate adverse effects
Adrenal Cortex Hormones adverse effects
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols adverse effects
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Prednisone adverse effects
Progression-Free Survival
Treatment Outcome
Abiraterone Acetate therapeutic use
Adrenal Cortex Hormones therapeutic use
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Prednisone therapeutic use
Prostatic Neoplasms, Castration-Resistant drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1573-0646
- Volume :
- 36
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Investigational new drugs
- Publication Type :
- Academic Journal
- Accession number :
- 30345466
- Full Text :
- https://doi.org/10.1007/s10637-018-0685-7