Other‐cause mortality in incidental prostate cancer

Author:

Di Bello Francesco12ORCID,Baudo Andrea134,de Angelis Mario156,Jannello Letizia Maria Ippolita147,Siech Carolin18,Tian Zhe1,Goyal Jordan A.1,Collà Ruvolo Claudia2ORCID,Califano Gianluigi2,La Rocca Roberto2,Morra Simone2ORCID,Acquati Pietro39,Saad Fred1,Shariat Shahrokh F.10111213,Carmignani Luca37,de Cobelli Ottavio47,Briganti Alberto56,Chun Felix K. H.8,Longo Nicola2,Karakiewicz Pierre I.1

Affiliation:

1. Cancer Prognostics and Health Outcomes Unit, Division of Urology University of Montréal Health Center Montréal Québec Canada

2. Department of Neurosciences, Science of Reproduction and Odontostomatology University of Naples Federico II Naples Italy

3. Department of Urology IRCCS Policlinico San Donato Milan Italy

4. Department of Urology IEO European Institute of Oncology, IRCCS Milan Italy

5. Division of Experimental Oncology/Unit of Urology, URI, Urological Research Institute IRCCS San Raffaele Scientific Institute Milan Italy

6. Department of Urology Vita‐Salute San Raffaele University Milan Italy

7. Università degli Studi di Milano Milan Italy

8. Goethe University Frankfurt, University Hospital Department of Urology Frankfurt am Main Germany

9. Department of Urology IRCCS Ospedale Galeazzi–Sant'Ambrogio Milan Italy

10. Department of Urology, Comprehensive Cancer Center Medical University of Vienna Vienna Austria

11. Department of Urology Weill Cornell Medical College New York New York USA

12. Department of Urology University of Texas Southwestern Medical Center Dallas Texas USA

13. Hourani Center for Applied Scientific Research Al‐Ahliyya Amman University Amman Jordan

Abstract

AbstractBackgroundIn incidental prostate cancer (IPCa), elevated other‐cause mortality (OCM) may obviate the need for active treatment. We tested OCM rates in IPCa according to treatment type and cancer grade and we hypothesized that OCM is significantly higher in not‐actively‐treated patients.MethodsWithin the Surveillance, Epidemiology, and End Results database (2004−2015), IPCa patients were identified. Smoothed cumulative incidence plots as well as multivariable competing risks regression models were fitted to address OCM after adjustment for cancer‐specific mortality (CSM).ResultsOf 5121 IPCa patients, 3655 (71%) were not‐actively‐treated while 1466 (29%) were actively‐treated. Incidental PCa not‐actively‐treated patients were older and exhibited higher proportion of Gleason sum (GS) 6 and clinical T1a stage. In smoothed cumulative incidence plots, 5‐year OCM was 20% for not‐actively‐treated versus 8% for actively‐treated patients. Conversely, 5‐year CSM was 5% for not‐actively‐treated versus 4% for actively‐treated patients. No active treatment was associated with 1.4‐fold higher OCM, even after adjustment for age, cancer characteristics, and CSM. According to GS, OCM reached 16%, 27%, and 35% in GS 6, 7, and 8−10 not‐actively‐treated IPCa patients, respectively and exceeded CSM recorded for the same three groups (2%, 6%, and 28%, respectively).ConclusionOur results quantified OCM rates, confirming that in not‐actively‐treated IPCa patients OCM is indeed significantly higher than in their actively‐treated counterparts (HR: 1.4). These observations validate the use of no active treatment in IPCa patients, in whom OCM greatly surpasses CSM (20% vs. 5%).

Publisher

Wiley

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