Mortality in men with castration-resistant prostate cancer-A long-term follow-up of a population-based real-world cohort.

PSA at time of CRPC PSA doubling time castration resistant prostate cancer mortality mortality in castration resistant prostate cancer natural history cohort real‐world cohort

Journal

BJUI compass
ISSN: 2688-4526
Titre abrégé: BJUI Compass
Pays: United States
ID NLM: 101764975

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 27 07 2021
accepted: 18 09 2021
entrez: 27 4 2022
pubmed: 28 4 2022
medline: 28 4 2022
Statut: epublish

Résumé

The objective of this study is to find clinical variables that predict the prognosis for men with castration-resistant prostate cancer (CRPC) in a Swedish real-life CRPC cohort, including a risk group classification to clarify the risk of succumbing to prostate cancer. This is a natural history cohort representing the premodern drug era before the introduction of novel hormonal drug therapies. PSA tests from the clinical chemistry laboratories serving health care in six regions of Sweden were retrieved and cross-linked to the National Prostate Cancer Registry (NPCR) to identify men with a prostate cancer diagnosis. Through further cross-linking with data sources at the Swedish Board of Health and Welfare, we retrieved other relevant information such as prescribed drugs, hospitalizations, and cause of death. Men entered the CRPC cohort at the first date of doubling of their PSA nadir value with the last value being >2 ng/ml, or an absolute increase of >5 ng/ml or more, whilst on 3 months of medical castration or if they had been surgically castrated ( PSA-DT and PSA at date of CRPC are the strongest variables associated with PC specific survival. At the end of follow-up, the proportion of men who died due to PC was 57%, 71%, 81%, 86%, and 89% for risk categories one through five, respectively. The median overall survival in our cohort of men with CRPC was 1.86 years (95% CI: 1.79-1.97). For a man with castration-resistant prostate cancer, there is a high probability that this will be the main cause contributing to his death. However, there is a significant difference in mortality that varies in relation to tumor burden assessed as PSA doubling time and PSA at time of CRCP. This information could be used in a clinical setting when deciding when to treat more or less aggressively once entering the CRPC phase of the disease.

Identifiants

pubmed: 35474724
doi: 10.1002/bco2.116
pii: BCO2116
pmc: PMC8988790
doi:

Types de publication

Journal Article

Langues

eng

Pagination

173-183

Informations de copyright

© 2021 The Authors. BJUI Compass published by John Wiley & Sons Ltd on behalf of BJU International Company.

Références

Clin Genitourin Cancer. 2017 Feb;15(1):60-66.e2
pubmed: 27692812
Clin Genitourin Cancer. 2018 Oct;16(5):402-412.e1
pubmed: 30126765
Cancer Epidemiol. 2015 Aug;39(4):623-32
pubmed: 26100365
Eur Urol Focus. 2019 Sep;5(5):842-848
pubmed: 29433987
Scand J Urol. 2020 Feb;54(1):20-26
pubmed: 31842658
N Engl J Med. 2014 Jul 31;371(5):424-33
pubmed: 24881730
N Engl J Med. 2004 Oct 7;351(15):1513-20
pubmed: 15470214
Eur J Cancer. 2015 Jan;51(1):101-11
pubmed: 25465187
Cancer Med. 2016 Feb;5(2):182-91
pubmed: 26710718
N Engl J Med. 2004 Oct 7;351(15):1502-12
pubmed: 15470213
N Engl J Med. 2015 Aug 20;373(8):737-46
pubmed: 26244877
Lancet. 2016 Mar 19;387(10024):1163-77
pubmed: 26719232
Lancet Oncol. 2012 Oct;13(10):983-92
pubmed: 22995653
Urology. 2016 Oct;96:171-176
pubmed: 27318265
Ther Adv Urol. 2017 Feb 06;9(3-4):81-88
pubmed: 28392837
Clin Cancer Res. 2008 Oct 1;14(19):6302-9
pubmed: 18829513
N Engl J Med. 2013 Jan 10;368(2):138-48
pubmed: 23228172
Eur J Clin Pharmacol. 2020 Apr;76(4):589-601
pubmed: 31925454
JAMA. 1982 May 14;247(18):2543-6
pubmed: 7069920
Int J Epidemiol. 2016 Feb;45(1):73-82
pubmed: 26659904
Acta Oncol. 2013 Nov;52(8):1593-601
pubmed: 23427879
BJUI Compass. 2021 Oct 10;3(2):173-183
pubmed: 35474724
Eur Urol. 2013 Aug;64(2):300-6
pubmed: 23313031
Scand J Urol. 2020 Oct;54(5):376-381
pubmed: 32734806
Eur Urol Focus. 2017 Oct;3(4-5):480-486
pubmed: 28753787
N Engl J Med. 2012 Sep 27;367(13):1187-97
pubmed: 22894553
BMC Cancer. 2019 Jan 14;19(1):60
pubmed: 30642291
Eur Urol Focus. 2018 Sep;4(5):694-701
pubmed: 28753794
N Engl J Med. 2019 Mar 28;380(13):1235-1246
pubmed: 30763142

Auteurs

Yashar Khoshkar (Y)

Department of Molecular Medicine and Surgery Karolinska Institute Stockholm Sweden.

Marcus Westerberg (M)

Department of Mathematics Uppsala University Uppsala Sweden.
Department of Surgical Sciences Uppsala University Uppsala Sweden.

Jan Adolfsson (J)

Department of Clinical Science, Intervention and Technology Karolinska Institute Stockholm Sweden.

Anna Bill-Axelson (A)

Department of Surgical Sciences Uppsala University Uppsala Sweden.

Henrik Olsson (H)

Department of Medical Epidemiology and Biostatistics Karolinska Institute Stockholm Sweden.

Martin Eklund (M)

Department of Medical Epidemiology and Biostatistics Karolinska Institute Stockholm Sweden.

Olof Akre (O)

Department of Molecular Medicine and Surgery Karolinska Institute Stockholm Sweden.
Prostate Cancer Flow, Patient Area Pelvic Cancer Karolinska Sjukhuset Solna Stockholm Sweden.

Hans Garmo (H)

Department of Surgical Sciences Uppsala University Uppsala Sweden.
Translational Oncology & Urology Research (TOUR), School of Cancer and Pharmaceutical Sciences King's College London London UK.
Regional Cancer Centre, Division of Central Sweden Uppsala Sweden.

Markus Aly (M)

Department of Molecular Medicine and Surgery Karolinska Institute Stockholm Sweden.
Prostate Cancer Flow, Patient Area Pelvic Cancer Karolinska Sjukhuset Solna Stockholm Sweden.

Classifications MeSH