Overall survival and second primary malignancies in men with metastatic prostate cancer.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 21 03 2019
accepted: 20 12 2019
entrez: 22 2 2020
pubmed: 23 2 2020
medline: 23 4 2020
Statut: epublish

Résumé

Among prostate cancer (PC) patients, over 90% of distant metastases occur in the bone. PC treatments may be associated with side effects, including second primary malignancies (SPM). There is limited information on the incidence of SPM among men with bone metastatic PC (mPC) and among men with bone metastatic castration-resistant PC (mCRPC). We estimated overall survival and the incidence of SPM in men with mPC and mCRPC. In the Prostate Cancer data Base Sweden, the National Prostate Cancer Register was linked to other national health care registers, 15,953 men with mPC in 1999-2011 were identified. Further, 693 men with mCRPC were identified. Outcomes were evaluated using stratified incidence rates, Kaplan-Meier estimators and Cox models. The mean age among men with mPC was 73.9 years and in men with mCRPC 70.0 years. The median respective survivals were 1.5 (13,965 deaths) and 1.14 years (599 deaths), and average times since PC diagnosis 1.8 and 4.7 years. We observed 2,669 SPMs in men with mPC and 100 SPMs in men with mCRPC. The incidence rate of SPM per 1,000 person-years was 81.8 (78.8-85.0) for mPC and 115.6 (95.1-140.7) for mCRPC. High age, prior neoplasms, urinary tract infection, congestive heart failure, diabetes and renal disease were most strongly associated with increased mortality risk. Prior neoplasms and prior use of antineoplastic agents were most strongly associated with increased SPM risk. Several factors associated with increased mortality and SPM risks were more prevalent in the mCRPC cohort. Our results on mortality for men with mPC and mCRPC are in line with previous studies from the same time period. Investigation of factors associated with mortality and SPM in men with mPC and mCRPC can help to further understand these outcomes in the era prior to several new treatments have come available.

Sections du résumé

BACKGROUND
Among prostate cancer (PC) patients, over 90% of distant metastases occur in the bone. PC treatments may be associated with side effects, including second primary malignancies (SPM). There is limited information on the incidence of SPM among men with bone metastatic PC (mPC) and among men with bone metastatic castration-resistant PC (mCRPC). We estimated overall survival and the incidence of SPM in men with mPC and mCRPC.
METHODS
In the Prostate Cancer data Base Sweden, the National Prostate Cancer Register was linked to other national health care registers, 15,953 men with mPC in 1999-2011 were identified. Further, 693 men with mCRPC were identified. Outcomes were evaluated using stratified incidence rates, Kaplan-Meier estimators and Cox models.
RESULTS
The mean age among men with mPC was 73.9 years and in men with mCRPC 70.0 years. The median respective survivals were 1.5 (13,965 deaths) and 1.14 years (599 deaths), and average times since PC diagnosis 1.8 and 4.7 years. We observed 2,669 SPMs in men with mPC and 100 SPMs in men with mCRPC. The incidence rate of SPM per 1,000 person-years was 81.8 (78.8-85.0) for mPC and 115.6 (95.1-140.7) for mCRPC. High age, prior neoplasms, urinary tract infection, congestive heart failure, diabetes and renal disease were most strongly associated with increased mortality risk. Prior neoplasms and prior use of antineoplastic agents were most strongly associated with increased SPM risk. Several factors associated with increased mortality and SPM risks were more prevalent in the mCRPC cohort.
CONCLUSIONS
Our results on mortality for men with mPC and mCRPC are in line with previous studies from the same time period. Investigation of factors associated with mortality and SPM in men with mPC and mCRPC can help to further understand these outcomes in the era prior to several new treatments have come available.

Identifiants

pubmed: 32084147
doi: 10.1371/journal.pone.0227552
pii: PONE-D-19-06361
pmc: PMC7034858
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0227552

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests: This study was supported by Bayer AG. ZV, JZ, GB and MSG are employed by Bayer. JM and HK are employees of EPID Research, a contract research organization that performs commissioned pharmacoepidemiologic studies in collaboration with several pharmaceutical companies. PS has no conflict of interests reported. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Références

Clin Prostate Cancer. 2003 Jun;2(1):41-5
pubmed: 15046683
Curr Oncol. 2010 Apr;17(2):24-9
pubmed: 20404974
Radiother Oncol. 2014 Feb;110(2):213-28
pubmed: 24485765
N Engl J Med. 2004 Oct 7;351(15):1513-20
pubmed: 15470214
J Clin Oncol. 2009 May 20;27(15):2450-6
pubmed: 19380444
Eur Urol. 2007 Feb;51(2):306-13; discussion 314
pubmed: 17007995
J Clin Oncol. 1989 May;7(5):590-7
pubmed: 2709088
J Clin Oncol. 2008 Mar 1;26(7):1148-59
pubmed: 18309951
J Urol. 2004 Apr;171(4):1525-8
pubmed: 15017212
Int J Radiat Oncol Biol Phys. 2006 Jul 1;65(3):637-9
pubmed: 16751057
Anticancer Res. 2011 Apr;31(4):1475-82
pubmed: 21508406
Br J Cancer. 2005 Sep 19;93(6):633-8
pubmed: 16222309
Int J Epidemiol. 2013 Aug;42(4):956-67
pubmed: 22561842
N Engl J Med. 2013 Jan 10;368(2):138-48
pubmed: 23228172
Lancet. 2000 Apr 29;355(9214):1491-8
pubmed: 10801170
PLoS One. 2014 Jul 21;9(7):e102596
pubmed: 25047238
N Engl J Med. 2013 Jul 18;369(3):213-23
pubmed: 23863050
BMJ. 2016 Mar 02;352:i851
pubmed: 26936410
Int J Clin Pract. 2011 Nov;65(11):1180-92
pubmed: 21995694
Eur Urol. 2015 Jun;67(6):1028-1038
pubmed: 25301760
J Urol. 2010 Jul;184(1):162-7
pubmed: 20483155
N Engl J Med. 2014 Jul 31;371(5):424-33
pubmed: 24881730
Eur J Nucl Med Mol Imaging. 2004 Jul;31(7):958-63
pubmed: 14985870
N Engl J Med. 2011 May 26;364(21):1995-2005
pubmed: 21612468
Eur Urol. 2008 Jan;53(1):68-80
pubmed: 17920184
Urology. 2009 May;73(5):1104-9
pubmed: 19394511
Cancer Invest. 2004;22(6):849-57
pubmed: 15641482
N Engl J Med. 1994 Oct 13;331(15):996-1004
pubmed: 7880240
Cancer. 2012 Dec 15;118(24):6207-16
pubmed: 22674346
Oncologist. 2003;8(2):161-73
pubmed: 12697941
Cancer. 1997 Apr 15;79(8):1600-4
pubmed: 9118045

Auteurs

Juha Mehtälä (J)

EPID Research, Espoo, Finland.

Jihong Zong (J)

Bayer LLC, Whippany, New Jersey, United States of America.

Zdravko Vassilev (Z)

Bayer LLC, Whippany, New Jersey, United States of America.

Gunnar Brobert (G)

Bayer AB, Stockholm, Sweden.

Montse Soriano Gabarró (MS)

Bayer AG, Berlin, Germany.

Pär Stattin (P)

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

Houssem Khanfir (H)

EPID Research, Espoo, Finland.

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Classifications MeSH