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Use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in Scotland
PURPOSE: New treatments are introduced into standard care based on clinical trial results. However, it is not clear if these benefits are reflected in the broader population. This study analysed the clinical outcomes of patients with metastatic castration‐resistant prostate cancer, treated with abir...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246935/ https://www.ncbi.nlm.nih.gov/pubmed/32316077 http://dx.doi.org/10.1002/pds.4998 |
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author | Baillie, Kelly Mueller, Tanja Pan, Jiafeng Laskey, Jennifer Bennie, Marion Crearie, Christine Kavanagh, Kimberley Alvarez‐Madrazo, Samantha Morrison, David Clarke, Julie Keel, Aileen Cameron, David Wu, Olivia Kurdi, Amanj Jones, Robert J. |
author_facet | Baillie, Kelly Mueller, Tanja Pan, Jiafeng Laskey, Jennifer Bennie, Marion Crearie, Christine Kavanagh, Kimberley Alvarez‐Madrazo, Samantha Morrison, David Clarke, Julie Keel, Aileen Cameron, David Wu, Olivia Kurdi, Amanj Jones, Robert J. |
author_sort | Baillie, Kelly |
collection | PubMed |
description | PURPOSE: New treatments are introduced into standard care based on clinical trial results. However, it is not clear if these benefits are reflected in the broader population. This study analysed the clinical outcomes of patients with metastatic castration‐resistant prostate cancer, treated with abiraterone and enzalutamide, within the Scottish National Health Service. METHODS: Retrospective cohort study using record linkage of routinely collected healthcare data (study period: February 2012 to February 2017). Overall survival (OS) was analysed using Kaplan‐Meier methods and Cox Proportional Hazard models; a subgroup analysis comprised potentially trial‐eligible patients. RESULTS: Overall, 271 patients were included and 73.8% died during the study period. Median OS was poorer than in the pivotal trials, regardless of medication and indication: 10.8 months (95% confidence interval [CI] 8.6‐15.1) and 20.9 months (95% CI 14.9‐29.0) for abiraterone, and 12.6 months (95% CI 10.5‐18.2) and 16.0 months (95% CI 9.8—not reached) for enzalutamide, post and pre chemotherapy, respectively. Only 46% of patients were potentially “trial eligible” and in this subgroup OS improved. Factors influencing survival included baseline performance status, and baseline prostate‐specific antigen, alkaline phosphatase, and albumin levels. CONCLUSIONS: Poorer prognostic features of non‐trial eligible patients impact real‐world outcomes of cancer medicines. Electronic record linkage of routinely collected healthcare data offers an opportunity to report outcomes on cancer medicines at scale and describe population demographics. The availability of such observational data to supplement clinical trial results enables patients and clinicians to make more informed treatment decisions, and policymakers to contextualise trial findings. |
format | Online Article Text |
id | pubmed-8246935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82469352021-07-02 Use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in Scotland Baillie, Kelly Mueller, Tanja Pan, Jiafeng Laskey, Jennifer Bennie, Marion Crearie, Christine Kavanagh, Kimberley Alvarez‐Madrazo, Samantha Morrison, David Clarke, Julie Keel, Aileen Cameron, David Wu, Olivia Kurdi, Amanj Jones, Robert J. Pharmacoepidemiol Drug Saf Original Reports PURPOSE: New treatments are introduced into standard care based on clinical trial results. However, it is not clear if these benefits are reflected in the broader population. This study analysed the clinical outcomes of patients with metastatic castration‐resistant prostate cancer, treated with abiraterone and enzalutamide, within the Scottish National Health Service. METHODS: Retrospective cohort study using record linkage of routinely collected healthcare data (study period: February 2012 to February 2017). Overall survival (OS) was analysed using Kaplan‐Meier methods and Cox Proportional Hazard models; a subgroup analysis comprised potentially trial‐eligible patients. RESULTS: Overall, 271 patients were included and 73.8% died during the study period. Median OS was poorer than in the pivotal trials, regardless of medication and indication: 10.8 months (95% confidence interval [CI] 8.6‐15.1) and 20.9 months (95% CI 14.9‐29.0) for abiraterone, and 12.6 months (95% CI 10.5‐18.2) and 16.0 months (95% CI 9.8—not reached) for enzalutamide, post and pre chemotherapy, respectively. Only 46% of patients were potentially “trial eligible” and in this subgroup OS improved. Factors influencing survival included baseline performance status, and baseline prostate‐specific antigen, alkaline phosphatase, and albumin levels. CONCLUSIONS: Poorer prognostic features of non‐trial eligible patients impact real‐world outcomes of cancer medicines. Electronic record linkage of routinely collected healthcare data offers an opportunity to report outcomes on cancer medicines at scale and describe population demographics. The availability of such observational data to supplement clinical trial results enables patients and clinicians to make more informed treatment decisions, and policymakers to contextualise trial findings. John Wiley & Sons, Inc. 2020-04-21 2020-06 /pmc/articles/PMC8246935/ /pubmed/32316077 http://dx.doi.org/10.1002/pds.4998 Text en © 2020 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Reports Baillie, Kelly Mueller, Tanja Pan, Jiafeng Laskey, Jennifer Bennie, Marion Crearie, Christine Kavanagh, Kimberley Alvarez‐Madrazo, Samantha Morrison, David Clarke, Julie Keel, Aileen Cameron, David Wu, Olivia Kurdi, Amanj Jones, Robert J. Use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in Scotland |
title | Use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in Scotland |
title_full | Use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in Scotland |
title_fullStr | Use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in Scotland |
title_full_unstemmed | Use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in Scotland |
title_short | Use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in Scotland |
title_sort | use of record linkage to evaluate treatment outcomes and trial eligibility in a real‐world metastatic prostate cancer population in scotland |
topic | Original Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246935/ https://www.ncbi.nlm.nih.gov/pubmed/32316077 http://dx.doi.org/10.1002/pds.4998 |
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