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Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer
BACKGROUND: Biomarkers of therapeutic response and prognosis are needed to assist in the sequencing of treatments for metastatic castration-resistant prostate cancer (CRPC). Previously in a Phase 1 discovery study, we identified 14 circulating microRNAs that were associated with response to docetaxe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396108/ https://www.ncbi.nlm.nih.gov/pubmed/28278515 http://dx.doi.org/10.1038/bjc.2017.50 |
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author | Lin, Hui-Ming Mahon, Kate L Spielman, Calan Gurney, Howard Mallesara, Girish Stockler, Martin R Bastick, Patricia Briscoe, Karen Marx, Gavin Swarbrick, Alexander Horvath, Lisa G |
author_facet | Lin, Hui-Ming Mahon, Kate L Spielman, Calan Gurney, Howard Mallesara, Girish Stockler, Martin R Bastick, Patricia Briscoe, Karen Marx, Gavin Swarbrick, Alexander Horvath, Lisa G |
author_sort | Lin, Hui-Ming |
collection | PubMed |
description | BACKGROUND: Biomarkers of therapeutic response and prognosis are needed to assist in the sequencing of treatments for metastatic castration-resistant prostate cancer (CRPC). Previously in a Phase 1 discovery study, we identified 14 circulating microRNAs that were associated with response to docetaxel chemotherapy or overall survival. We performed a Phase 2 validation study to verify these findings. METHODS: Using real-time PCR, the levels of the 14 microRNAs were measured in plasma collected before and after the first cycle of docetaxel from a Phase 2 cohort of 89 patients. RESULTS: The microRNAs were not associated with docetaxel response in the Phase 2 cohort. Higher baseline levels of six microRNAs, predominantly of the miR-200 family, were confirmed to be associated with shorter overall survival. A microRNA signature comprising these six microRNAs predicted high-risk patients in the Phase 2 cohort with a hazard ratio of 4.12 (95% CI 2.20–7.70, P=0.000001). The signature was an independent predictor in multivariable analysis with clinicopathological factors. CONCLUSIONS: The association of circulating microRNAs with overall survival suggests their involvement in CRPC progression. |
format | Online Article Text |
id | pubmed-5396108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53961082018-04-11 Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer Lin, Hui-Ming Mahon, Kate L Spielman, Calan Gurney, Howard Mallesara, Girish Stockler, Martin R Bastick, Patricia Briscoe, Karen Marx, Gavin Swarbrick, Alexander Horvath, Lisa G Br J Cancer Clinical Study BACKGROUND: Biomarkers of therapeutic response and prognosis are needed to assist in the sequencing of treatments for metastatic castration-resistant prostate cancer (CRPC). Previously in a Phase 1 discovery study, we identified 14 circulating microRNAs that were associated with response to docetaxel chemotherapy or overall survival. We performed a Phase 2 validation study to verify these findings. METHODS: Using real-time PCR, the levels of the 14 microRNAs were measured in plasma collected before and after the first cycle of docetaxel from a Phase 2 cohort of 89 patients. RESULTS: The microRNAs were not associated with docetaxel response in the Phase 2 cohort. Higher baseline levels of six microRNAs, predominantly of the miR-200 family, were confirmed to be associated with shorter overall survival. A microRNA signature comprising these six microRNAs predicted high-risk patients in the Phase 2 cohort with a hazard ratio of 4.12 (95% CI 2.20–7.70, P=0.000001). The signature was an independent predictor in multivariable analysis with clinicopathological factors. CONCLUSIONS: The association of circulating microRNAs with overall survival suggests their involvement in CRPC progression. Nature Publishing Group 2017-04-11 2017-03-09 /pmc/articles/PMC5396108/ /pubmed/28278515 http://dx.doi.org/10.1038/bjc.2017.50 Text en Copyright © 2017 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Clinical Study Lin, Hui-Ming Mahon, Kate L Spielman, Calan Gurney, Howard Mallesara, Girish Stockler, Martin R Bastick, Patricia Briscoe, Karen Marx, Gavin Swarbrick, Alexander Horvath, Lisa G Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer |
title | Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer |
title_full | Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer |
title_fullStr | Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer |
title_full_unstemmed | Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer |
title_short | Phase 2 study of circulating microRNA biomarkers in castration-resistant prostate cancer |
title_sort | phase 2 study of circulating microrna biomarkers in castration-resistant prostate cancer |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396108/ https://www.ncbi.nlm.nih.gov/pubmed/28278515 http://dx.doi.org/10.1038/bjc.2017.50 |
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