Fatigue, treatment satisfaction and health-related quality of life among patients receiving novel drugs suppressing androgen signalling for the treatment of metastatic castrate-resistant prostate cancer.


Journal

European journal of cancer care
ISSN: 1365-2354
Titre abrégé: Eur J Cancer Care (Engl)
Pays: England
ID NLM: 9301979

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 27 05 2016
revised: 23 03 2017
accepted: 24 08 2018
pubmed: 9 11 2018
medline: 15 5 2019
entrez: 9 11 2018
Statut: ppublish

Résumé

Clinical studies have demonstrated the benefits of abiraterone acetate + prednisone (AAP) and enzalutamide (ENZ) in significantly improving survival among metastatic castration-resistant prostate cancer (mCRPC) patients. However, evidence regarding patient's real-world experience, particularly with respect to fatigue, treatment satisfaction and health-related quality of life (HRQoL) is limited. Interviews were initially conducted with patients (n = 38) and carers (n = 12) to elicit qualitative data regarding their experiences. Findings informed the design of a quantitative, multinational online survey of mCRPC patients (n = 152) receiving AAP or ENZ. Participants completed validated questionnaires assessing fatigue (Brief Fatigue Inventory), treatment satisfaction (Cancer Therapy Satisfaction Questionnaire) and HRQoL (EuroQol-5-Dimensions). Results indicated that patients were generally satisfied with these therapies, more specifically with reductions in prostate-specific antigen levels and extended survival. Fatigue was commonly linked to poor HRQoL and responses indicated that significantly fewer patients in the AAP group reported feeling usually tired or fatigued in the last week compared to the ENZ group (33% vs. 55%, p = 0.006 respectively). Findings highlight the benefit of AAP and ENZ in promoting the "quality" of extended survival. That fatigue was lower among patients receiving AAP may be important for informing treatment decisions. Further research is needed to gain deeper insights.

Identifiants

pubmed: 30408244
doi: 10.1111/ecc.12949
doi:

Substances chimiques

Antineoplastic Agents 0
Benzamides 0
Nitriles 0
Phenylthiohydantoin 2010-15-3
enzalutamide 93T0T9GKNU
Abiraterone Acetate EM5OCB9YJ6
Prednisone VB0R961HZT

Types de publication

Journal Article

Langues

eng

Pagination

e12949

Subventions

Organisme : Janssen Pharmaceuticals

Informations de copyright

© 2018 John Wiley & Sons Ltd.

Auteurs

Lindsay Dearden (L)

Janssen EMEA HEMAR, High Wycombe, UK.

Natalie Shalet (N)

Janssen EMEA HEMAR, High Wycombe, UK.

Cristiana Artenie (C)

Adelphi Research UK, Bollington, UK.

Andrew Mills (A)

Adelphi Research UK, Bollington, UK.

Claire Jackson (C)

Adelphi Research UK, Bollington, UK.

Laura Grant (L)

Adelphi Values, Bollington, UK.

Adam Gater (A)

Adelphi Values, Bollington, UK.

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Classifications MeSH