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Effect of abiraterone acetate plus prednisone on the QT interval in patients with metastatic castration-resistant prostate cancer
PURPOSE: Abiraterone is the active metabolite of the pro-drug abiraterone acetate (AA) and a selective inhibitor of CYP17, a key enzyme in testosterone synthesis, and improves overall survival in postdocetaxel metastatic castration-resistant prostate cancer (mCRPC). This open-label, single-arm phase...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405235/ https://www.ncbi.nlm.nih.gov/pubmed/22752297 http://dx.doi.org/10.1007/s00280-012-1916-9 |
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author | Tolcher, A. W. Chi, K. N. Shore, N. D. Pili, R. Molina, A. Acharya, M. Kheoh, T. Jiao, J. J. Gonzalez, M. Trinh, A. Pankras, C. Tran, N. |
author_facet | Tolcher, A. W. Chi, K. N. Shore, N. D. Pili, R. Molina, A. Acharya, M. Kheoh, T. Jiao, J. J. Gonzalez, M. Trinh, A. Pankras, C. Tran, N. |
author_sort | Tolcher, A. W. |
collection | PubMed |
description | PURPOSE: Abiraterone is the active metabolite of the pro-drug abiraterone acetate (AA) and a selective inhibitor of CYP17, a key enzyme in testosterone synthesis, and improves overall survival in postdocetaxel metastatic castration-resistant prostate cancer (mCRPC). This open-label, single-arm phase 1b study was conducted to assess the effect of AA and abiraterone on the QT interval. METHODS: The study was conducted in 33 patients with mCRPC. Patients received AA 1,000 mg orally once daily + prednisone 5 mg orally twice daily. Electrocardiograms (ECGs) were collected in triplicate using 12-lead Holter monitoring. Baseline ECGs were obtained on Cycle 1 Day-1. Serial ECG recordings and time-matched pharmacokinetic (PK) blood samples were collected over 24 h on Cycle 1 Day 1 and Cycle 2 Day 1. Serial PK blood samples were also collected over 24 h on Cycle 1 Day 8. RESULTS: After AA administration, the upper bound of the 2-sided 90 % confidence interval (CI) for the mean baseline-adjusted QTcF change was <10 ms; no patients discontinued due to QTc prolongation or adverse events. No apparent relationship between change in QTcF and abiraterone plasma concentrations was observed [estimated slope (90 % CI): 0.0031 (−0.0040, 0.0102)]. CONCLUSIONS: There is no significant effect of AA plus prednisone on the QT/QTc interval in patients with mCRPC. |
format | Online Article Text |
id | pubmed-3405235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-34052352012-08-02 Effect of abiraterone acetate plus prednisone on the QT interval in patients with metastatic castration-resistant prostate cancer Tolcher, A. W. Chi, K. N. Shore, N. D. Pili, R. Molina, A. Acharya, M. Kheoh, T. Jiao, J. J. Gonzalez, M. Trinh, A. Pankras, C. Tran, N. Cancer Chemother Pharmacol Original Article PURPOSE: Abiraterone is the active metabolite of the pro-drug abiraterone acetate (AA) and a selective inhibitor of CYP17, a key enzyme in testosterone synthesis, and improves overall survival in postdocetaxel metastatic castration-resistant prostate cancer (mCRPC). This open-label, single-arm phase 1b study was conducted to assess the effect of AA and abiraterone on the QT interval. METHODS: The study was conducted in 33 patients with mCRPC. Patients received AA 1,000 mg orally once daily + prednisone 5 mg orally twice daily. Electrocardiograms (ECGs) were collected in triplicate using 12-lead Holter monitoring. Baseline ECGs were obtained on Cycle 1 Day-1. Serial ECG recordings and time-matched pharmacokinetic (PK) blood samples were collected over 24 h on Cycle 1 Day 1 and Cycle 2 Day 1. Serial PK blood samples were also collected over 24 h on Cycle 1 Day 8. RESULTS: After AA administration, the upper bound of the 2-sided 90 % confidence interval (CI) for the mean baseline-adjusted QTcF change was <10 ms; no patients discontinued due to QTc prolongation or adverse events. No apparent relationship between change in QTcF and abiraterone plasma concentrations was observed [estimated slope (90 % CI): 0.0031 (−0.0040, 0.0102)]. CONCLUSIONS: There is no significant effect of AA plus prednisone on the QT/QTc interval in patients with mCRPC. Springer-Verlag 2012-07-03 2012 /pmc/articles/PMC3405235/ /pubmed/22752297 http://dx.doi.org/10.1007/s00280-012-1916-9 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Tolcher, A. W. Chi, K. N. Shore, N. D. Pili, R. Molina, A. Acharya, M. Kheoh, T. Jiao, J. J. Gonzalez, M. Trinh, A. Pankras, C. Tran, N. Effect of abiraterone acetate plus prednisone on the QT interval in patients with metastatic castration-resistant prostate cancer |
title | Effect of abiraterone acetate plus prednisone on the QT interval in patients with metastatic castration-resistant prostate cancer |
title_full | Effect of abiraterone acetate plus prednisone on the QT interval in patients with metastatic castration-resistant prostate cancer |
title_fullStr | Effect of abiraterone acetate plus prednisone on the QT interval in patients with metastatic castration-resistant prostate cancer |
title_full_unstemmed | Effect of abiraterone acetate plus prednisone on the QT interval in patients with metastatic castration-resistant prostate cancer |
title_short | Effect of abiraterone acetate plus prednisone on the QT interval in patients with metastatic castration-resistant prostate cancer |
title_sort | effect of abiraterone acetate plus prednisone on the qt interval in patients with metastatic castration-resistant prostate cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405235/ https://www.ncbi.nlm.nih.gov/pubmed/22752297 http://dx.doi.org/10.1007/s00280-012-1916-9 |
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