Impact of Novel Hormonal Agents (Abiraterone, Enzalutamide) on the Development of Visceral and/or Brain Metastases in Patients With Bone-metastatic Castration-resistant Prostate Cancer.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
10 2022
Historique:
received: 29 12 2021
revised: 11 04 2022
accepted: 14 04 2022
pubmed: 14 5 2022
medline: 28 9 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

The overall survival (OS) of metastatic castration-resistant prostate cancer (mCRPC) patients has improved since 2011 with the use of novel hormonal agents (NHAs). The incidence of brain metastases (mets) has been reported to increase since 2004 with the use of docetaxel, but not the incidence of visceral mets. Our objective was to study whether the use of NHAs increases the risk of developing visceral or brain mets (VBMs). mCRPC patients with mets limited to bone (bmCRPC), treated at Tours University Hospital between 2007 and 2015, were included retrospectively. The primary endpoint was to determine whether treatment with NHAs was associated with an increased incidence of VBMs. Secondary endpoints included the search for putative predictive factors to develop VBMs. On 187 bmCRPC patients included, 65 developed VBMs. VBM incidence increased in bmCRPC patients alive after 2011, compared to patients who died before (39.7 vs. 24.6%, P = .04). Meanwhile, their median OS increased from 16.3 months to 28.5 months (P = .01). The longer was the treatment with NHAs, the lower was the risk of VBMs (HR = 0.96, 95% CI [0.94; 0.99]), whereas age < 70 years (HR = 3.33, 95% CI [1.50; 7.40]) and low PSA level at diagnosis (HR = 1.58, 95% CI [1.16; 2.15]) increased this risk. Though retrospective, our results showed an increased incidence of VBMs in bmCRPC patients after 2011. However, this was not associated with NHA exposure duration. The role of NHA exposure remains unclear and needs further investigation.

Identifiants

pubmed: 35562276
pii: S1558-7673(22)00082-9
doi: 10.1016/j.clgc.2022.04.004
pii:
doi:

Substances chimiques

Androstenes 0
Benzamides 0
Nitriles 0
Docetaxel 15H5577CQD
Phenylthiohydantoin 2010-15-3
enzalutamide 93T0T9GKNU
Prostate-Specific Antigen EC 3.4.21.77
Abiraterone Acetate EM5OCB9YJ6
abiraterone G819A456D0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

495.e1-495.e9

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Auteurs

Cédric Pobel (C)

Department of Medical Oncology, CHU Bretonneau Centre, Tours University, Tours, France.

Emeline Laurent (E)

Department of Epidemiology, CHU Bretonneau Centre, Tours University, Tours, France.

Aline-Marie Florence (AM)

Department of Epidemiology, CHU Bretonneau Centre, Tours University, Tours, France.

Gaëlle Fromont (G)

Department of Anatomical Pathology, CHU Bretonneau Centre, Tours University, Tours, France.

Gilles Calais (G)

Department of Radiotherapy, CHU Bretonneau Centre, Tours University, Tours, France.

Bérengère Narciso (B)

Department of Medical Oncology, CHU Bretonneau Centre, Tours University, Tours, France.

Claude Linassier (C)

Department of Medical Oncology, CHU Bretonneau Centre, Tours University, Tours, France.

Mathilde Cancel (M)

Department of Medical Oncology, CHU Bretonneau Centre, Tours University, Tours, France. Electronic address: m.cancel@chu-tours.fr.

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Classifications MeSH