Neurocognitive effects of androgen deprivation therapy and new hormonal agents in a sample of patients with metastatic prostate cancer.

Androgen deprivation therapy Hormonal agents Metastatic prostate cancer Neurocognitive effects

Journal

International urology and nephrology
ISSN: 1573-2584
Titre abrégé: Int Urol Nephrol
Pays: Netherlands
ID NLM: 0262521

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 09 05 2023
accepted: 12 07 2023
pubmed: 19 7 2023
medline: 19 7 2023
entrez: 19 7 2023
Statut: ppublish

Résumé

Although the growing treatment landscape for metastatic prostate cancer (mPC) has revealed new opportunities, it has also provided challenges, such as undesirable side effects. The aim of the present study was to provide further data on domain-specific cognitive impairments in mPC patients with androgen deprivation therapy (ADT) and new hormonal agents. Fifty-eight patients (71 ± 8 years) with mPC were investigated using a cross-sectional design. All patients had received some form of ADT (93% had received luteinizing hormone-releasing hormone (LHRH) analogs/antagonists), 66% had received chemotherapy, and 84% had received anti-resorptive therapy. We evaluated learning and memory, processing speed, and executive functions, as recommended by the International Cognition and Cancer Task Force, to determine neurocognitive deficits. Patients treated with ADT scored significantly lower on all neurocognitive tests and showed significantly more neurocognitive deficits (38-62%) than age-adjusted reference samples (16%, p < 0.05). Cognitive deficits were mild in most cases and predominantly affected visuomotor processing speed (48%). Moderate and severe deficits were found in 11% and 5% of patients, respectively, with word fluency as the predominant deficit (23%). No associations were found between the type or duration of treatment and the severity of cognitive deficits. Treatment of mPC with ADT is correlated with neurocognitive deficits in several cognitive domains. Language skills and processing speed were most frequently impaired. However, a consistent pattern of cognitive impairment was not identified. Neurocognitive deficits should be considered in phase III and IV trials. The study was registered in the German Clinical Trials Registry (DRKS00017727).

Identifiants

pubmed: 37466904
doi: 10.1007/s11255-023-03712-z
pii: 10.1007/s11255-023-03712-z
pmc: PMC10560187
doi:

Banques de données

DRKS
['DRKS00017727']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2733-2739

Informations de copyright

© 2023. The Author(s).

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Auteurs

Andreas Ihrig (A)

Division of Psycho-Oncology, Department of General Internal Medicine and Psychosomatics, University Hospital Heidelberg, INF 410, 69120, Heidelberg, Germany. andreas.ihrig@med.uni-heidelberg.de.

Pascal Marino Pernt (PM)

Division of Psycho-Oncology, Department of General Internal Medicine and Psychosomatics, University Hospital Heidelberg, INF 410, 69120, Heidelberg, Germany.

Stefanie Zschäbitz (S)

Department of Medical Oncology, National Centre for Tumor Diseases (NCT), University Hospital Heidelberg, Heidelberg, Germany.

Johannes Huber (J)

Department of Urology, Philipps-University Marburg, Marburg, Germany.

Hans-Christoph Friederich (HC)

Division of Psycho-Oncology, Department of General Internal Medicine and Psychosomatics, University Hospital Heidelberg, INF 410, 69120, Heidelberg, Germany.

Till J Bugaj (TJ)

Division of Psycho-Oncology, Department of General Internal Medicine and Psychosomatics, University Hospital Heidelberg, INF 410, 69120, Heidelberg, Germany.

Imad Maatouk (I)

Division of Psycho-Oncology, Department of General Internal Medicine and Psychosomatics, University Hospital Heidelberg, INF 410, 69120, Heidelberg, Germany.
Section of Psychosomatic Medicine, Psychotherapy and Psycho-Oncology, Department of Internal Medicine II, Julius-Maximilian University Würzburg, Würzburg, Germany.

Classifications MeSH