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Impact of visceral metastases on outcome to abiraterone after docetaxel in castration-resistant prostate cancer patients.
- Source :
-
Future oncology (London, England) [Future Oncol] 2015; Vol. 11 (21), pp. 2881-91. Date of Electronic Publication: 2015 Oct 05. - Publication Year :
- 2015
-
Abstract
- Background: The objective of this study was to analyze the impact of visceral metastases in castration-resistant prostate cancer (CRPC) treated with abiraterone.<br />Materials & Methods: All CRPC patients received abiraterone 1000 mg daily plus prednisone 10 mg orally daily. Liver and lung metastases were considered as visceral metastases.<br />Results: Of 265 CRPC patients, 49 had visceral metastases. Results on progression-free survival were not significantly different in patients with or without visceral metastases. Conversely, the median overall survival between the two groups was 12.4 and 18.5 months (p = 0.01), respectively, and median overall survival of patients with liver-only disease versus other sites was 10.5 versus 18.5 months (p = 0.006), respectively.<br />Conclusion: Visceral disease appears to be an important predictor of clinical outcome in CRPC patients treated with abiraterone.
- Subjects :
- Aged
Aged, 80 and over
Androstenes pharmacology
Antineoplastic Agents, Hormonal pharmacology
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Docetaxel
Humans
Male
Middle Aged
Neoplasm Metastasis
Prostatic Neoplasms, Castration-Resistant mortality
Retrospective Studies
Survival Analysis
Taxoids administration & dosage
Treatment Outcome
Androstenes therapeutic use
Antineoplastic Agents, Hormonal therapeutic use
Prostatic Neoplasms, Castration-Resistant drug therapy
Prostatic Neoplasms, Castration-Resistant pathology
Viscera pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1744-8301
- Volume :
- 11
- Issue :
- 21
- Database :
- MEDLINE
- Journal :
- Future oncology (London, England)
- Publication Type :
- Academic Journal
- Accession number :
- 26436290
- Full Text :
- https://doi.org/10.2217/fon.15.158