Please use this identifier to cite or link to this item: https://doi.org/10.4137/CMO.S13671
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dc.titleHormonal therapeutics enzalutamide and abiraterone acetate in the treatment of metastatic castration-resistant prostate cancer (mCRPC) post-docetaxel-an indirect comparison
dc.contributor.authorTan, P.S.
dc.contributor.authorHaaland, B.
dc.contributor.authorMontero, A.J.
dc.contributor.authorKyriakopoulos, C.E.
dc.contributor.authorLopes, G.
dc.date.accessioned2016-09-06T03:00:02Z
dc.date.available2016-09-06T03:00:02Z
dc.date.issued2014-03-16
dc.identifier.citationTan, P.S., Haaland, B., Montero, A.J., Kyriakopoulos, C.E., Lopes, G. (2014-03-16). Hormonal therapeutics enzalutamide and abiraterone acetate in the treatment of metastatic castration-resistant prostate cancer (mCRPC) post-docetaxel-an indirect comparison. Clinical Medicine Insights: Oncology 8 : 29-36. ScholarBank@NUS Repository. https://doi.org/10.4137/CMO.S13671
dc.identifier.issn11795549
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/126501
dc.description.abstractIntroduction: This study aims to make an indirect comparison between enzalutamide and abiraterone acetate for mCRPC post-docetaxel. Methods: A search for published phase 3 trials was performed with PubMed. Indirect comparisons of enzalutamide (AFFIRM) to abiraterone acetate (COU-AA-301) on outcomes overall survival (OS), time to prostate-specific-antigen (PSA) progression, radiographic progression-free survival (PFS), and PSA response were constructed in the context of log-linear regression models. Results: There was no statistically significant difference in OS (hazard ratio (HR) 0.85, 95% CI 0.68-1.07). However, there was some evidence that enzalutamide may outperform abiraterone acetate with respect to secondary outcomes: time to PSA progression (HR 0.40, 95% CI 0.30-0.53), radiographic PFS (HR 0.61, 95% CI 0.50-0.74), and PSA response rates (RRs) (OR 10.69, 95% CI 3.92-29.20). Conclusion: While there was no statistically significant difference in OS, enzalutamide may be advantageous for secondary endpoints. Findings of this indirect comparison serve to be hypothesis-generating for future head-to-head trials. © the authors.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.4137/CMO.S13671
dc.sourceScopus
dc.subjectAbiraterone acetate
dc.subjectEnzalutamide
dc.subjectmCRPC
dc.subjectMetastatic castration-resistant prostate cancer
dc.subjectPost-docetaxel
dc.typeArticle
dc.contributor.departmentDUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
dc.description.doi10.4137/CMO.S13671
dc.description.sourcetitleClinical Medicine Insights: Oncology
dc.description.volume8
dc.description.page29-36
dc.identifier.isiut000215745000004
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