Clinical characteristics and outcomes for patients with non‑metastatic castration-resistant prostate cancer
Clinical characteristics and outcomes for patients with non‑metastatic castration-resistant prostate cancer
This study used linked, routinely-collected datasets to explore incidence, clinical characteristics and outcomes of prostate cancer (PC) patients who experience a rise in prostate-specific antigen (PSA) levels despite androgen deprivation therapy (ADT), without evidence of metastases in their patient record, termed non-metastatic castration-resistant PC (nmCRPC). Routinely collected administrative data in Wales were used to identify patients diagnosed with PC and nmCRPC from 2000-2015. Logrank tests and Cox proportional hazard models were used to compare time-to-events across subgroups defined by PSA doubling time and age. Of 38,021 patients identified with PC, 1,465 met nmCRPC criteria. PC incidence increased over the study period, while nmCRPC categorizations reduced. Median time from PC diagnosis to nmCRPC categorization was 3.07 years (95% confidence interval [CI] 2.91-3.26) and from nmCRPC categorization to metastases/death was 2.86 years (95% CI 2.67-3.09). Shorter PSA doubling time (≤ 10 months, versus > 10 months) was associated with reduced time to metastases or death (2.11 years [95% CI 1.92-2.30] versus 5.22 years [95% CI 4.87-5.51]). Age was not significantly associated with time to metastases/death. Our findings highlight key clinical characteristics and outcomes for patients with nmCRPC prior to the introduction of recently approved treatments.
Arnold, Peter
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Penaloza-Ramos, Maria Cristina
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Adedokun, Lola
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Rees, Sarah
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Lockhat, Mohamed
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Spary, Lisa
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Watkins, Alan
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Gnanapragasam, Vincent
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Crabb, Simon J
bcd1b566-7677-4f81-8429-3ab0e85f8373
12 November 2021
Arnold, Peter
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Penaloza-Ramos, Maria Cristina
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Adedokun, Lola
72045e05-218c-4cdb-bdc1-fe154338b012
Rees, Sarah
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Lockhat, Mohamed
443ff477-7118-4b4a-99f3-1d89b0e02fcf
Spary, Lisa
946a8a70-43d4-4e74-9cde-f1adb9896764
Watkins, Alan
a9d13ba8-1de6-4917-863f-f4d8fb34e1e6
Gnanapragasam, Vincent
64250a97-e490-4c9f-b2ab-2a97a0a35a24
Crabb, Simon J
bcd1b566-7677-4f81-8429-3ab0e85f8373
Arnold, Peter, Penaloza-Ramos, Maria Cristina, Adedokun, Lola, Rees, Sarah, Lockhat, Mohamed, Spary, Lisa, Watkins, Alan, Gnanapragasam, Vincent and Crabb, Simon J
(2021)
Clinical characteristics and outcomes for patients with non‑metastatic castration-resistant prostate cancer.
Scientific Reports, 11 (1), [22151].
(doi:10.1038/s41598-021-01042-7).
Abstract
This study used linked, routinely-collected datasets to explore incidence, clinical characteristics and outcomes of prostate cancer (PC) patients who experience a rise in prostate-specific antigen (PSA) levels despite androgen deprivation therapy (ADT), without evidence of metastases in their patient record, termed non-metastatic castration-resistant PC (nmCRPC). Routinely collected administrative data in Wales were used to identify patients diagnosed with PC and nmCRPC from 2000-2015. Logrank tests and Cox proportional hazard models were used to compare time-to-events across subgroups defined by PSA doubling time and age. Of 38,021 patients identified with PC, 1,465 met nmCRPC criteria. PC incidence increased over the study period, while nmCRPC categorizations reduced. Median time from PC diagnosis to nmCRPC categorization was 3.07 years (95% confidence interval [CI] 2.91-3.26) and from nmCRPC categorization to metastases/death was 2.86 years (95% CI 2.67-3.09). Shorter PSA doubling time (≤ 10 months, versus > 10 months) was associated with reduced time to metastases or death (2.11 years [95% CI 1.92-2.30] versus 5.22 years [95% CI 4.87-5.51]). Age was not significantly associated with time to metastases/death. Our findings highlight key clinical characteristics and outcomes for patients with nmCRPC prior to the introduction of recently approved treatments.
Text
nmCRPC Manuscript_SR_Submission_revised submission_CLEAN
- Accepted Manuscript
More information
Accepted/In Press date: 21 October 2021
e-pub ahead of print date: 12 November 2021
Published date: 12 November 2021
Additional Information:
Funding Information:
The authors thank the investigators and their teams who took part in this study. The authors also acknowledge Maria Cristina Penaloza-Ramos, PhD, Janssen, for publication coordination and Cicely Kerr, PhD, Janssen, for aiding the funding for medical writing support. Furthermore, the authors acknowledge Olivia Wakeman, BSc, and Emma Phillips, PhD, from Costello Medical, Cambridge, UK, for medical writing and editorial assistance based on the authors’ input and direction. This study makes use of anonymised data held in the Secure Anonymised Information Linkage (SAIL) system, which is part of the national e-health records research infrastructure for Wales. We would like to acknowledge all the data providers who make anonymised data available for research. This study was funded by Janssen.
Funding Information:
PA: Research funding from Janssen-Cilag Ltd; MCPR, LA, ML: Employees of Janssen-Cilag Ltd; SR: Research funding from Janssen-Cilag Ltd; LS: None to declare; AW: Research funding from Janssen-Cilag Ltd; VG: Consulting fees and honoraria from Janssen-Cilag Ltd; SJC: Honoraria or advisory roles: Astellas, AstraZeneca, Bayer, Beigene, Brandcast Health, Clovis Oncology, Janssen-Cilag Ltd, MSD, Pfizer, Roche; Research support: Astex Pharmaceuticals, AstraZeneca, Clovis Oncology.
Publisher Copyright:
© 2021, The Author(s).
Identifiers
Local EPrints ID: 453240
URI: http://eprints.soton.ac.uk/id/eprint/453240
ISSN: 2045-2322
PURE UUID: 9895702d-44fc-4963-a113-eac36391a72e
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Date deposited: 11 Jan 2022 17:43
Last modified: 17 Mar 2024 02:57
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Contributors
Author:
Peter Arnold
Author:
Maria Cristina Penaloza-Ramos
Author:
Lola Adedokun
Author:
Sarah Rees
Author:
Mohamed Lockhat
Author:
Lisa Spary
Author:
Alan Watkins
Author:
Vincent Gnanapragasam
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