Physical function patient-reported outcomes among adolescent and young adult cancer survivors: A systematic review.

adolescent cancer cancer survivors patient‐reported outcome measures physical function routinely collected health data young adult

Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
Mar 2024
Historique:
revised: 19 01 2024
received: 27 10 2023
accepted: 13 02 2024
medline: 23 3 2024
pubmed: 23 3 2024
entrez: 23 3 2024
Statut: ppublish

Résumé

The physical challenges faced by adolescents and young adults (AYA) after a cancer diagnosis may be different from those experienced by paediatric and older adult cancer patients. Patient-reported outcome measures (PROMs) are valuable tools that can be useful in exploring the experiences of AYAs and identifying important issues, recurrent themes and areas to potentially improve quality of life. We compared patient-reported physical function outcomes between AYAs diagnosed with cancer and non-cancer controls. This paper builds on a scoping review published in early 2023 and focuses on PROMs related to physical function. This systematic review includes 16 studies that measured and reported on physical function PROMs in AYA cancer survivors compared with their cancer-free peers. Of these studies, 14 found that physical function in AYA survivors was significantly worse. This paper also includes a meta-analysis conducted on 5 studies using the EORTC-QLQ-C30 to measure physical function, which found that physical function score was an average of 7.03 (95% CI: -10.21, -3.86) points lower in the AYA cancer group, compared to their cancer free-peers, a difference that is clinically meaningful. The results overwhelmingly demonstrate that AYAs post a cancer diagnosis have worse health-related quality of life from a physical function perspective than their cancer-free peers, providing a compelling argument for the need to address this issue. All but one of the studies were cross-sectional, which highlights the need for further assessment of this group longitudinally throughout their cancer journey.

Sections du résumé

BACKGROUND BACKGROUND
The physical challenges faced by adolescents and young adults (AYA) after a cancer diagnosis may be different from those experienced by paediatric and older adult cancer patients. Patient-reported outcome measures (PROMs) are valuable tools that can be useful in exploring the experiences of AYAs and identifying important issues, recurrent themes and areas to potentially improve quality of life.
OBJECTIVE OBJECTIVE
We compared patient-reported physical function outcomes between AYAs diagnosed with cancer and non-cancer controls.
METHOD METHODS
This paper builds on a scoping review published in early 2023 and focuses on PROMs related to physical function.
RESULTS RESULTS
This systematic review includes 16 studies that measured and reported on physical function PROMs in AYA cancer survivors compared with their cancer-free peers. Of these studies, 14 found that physical function in AYA survivors was significantly worse. This paper also includes a meta-analysis conducted on 5 studies using the EORTC-QLQ-C30 to measure physical function, which found that physical function score was an average of 7.03 (95% CI: -10.21, -3.86) points lower in the AYA cancer group, compared to their cancer free-peers, a difference that is clinically meaningful.
CONCLUSIONS CONCLUSIONS
The results overwhelmingly demonstrate that AYAs post a cancer diagnosis have worse health-related quality of life from a physical function perspective than their cancer-free peers, providing a compelling argument for the need to address this issue. All but one of the studies were cross-sectional, which highlights the need for further assessment of this group longitudinally throughout their cancer journey.

Identifiants

pubmed: 38520164
doi: 10.1002/cam4.7046
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e7046

Informations de copyright

© 2024 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Sarah Tanner (S)

Centre for Health Services Research, The University of Queensland, Herston, Queensland, Australia.

Teyl Engstrom (T)

Centre for Health Services Research, The University of Queensland, Herston, Queensland, Australia.

Cheryl Forbes (C)

Centre for Health Services Research, The University of Queensland, Herston, Queensland, Australia.

Dhaval Patel (D)

Centre for Health Services Research, The University of Queensland, Herston, Queensland, Australia.

Wen Ray Lee (WR)

Child Health Research Centre, The University of Queensland, South Brisbane, Queensland, Australia.

Rick Walker (R)

School of Medicine, The University of Queensland, Herston, Queensland, Australia.
Queensland Children's Hospital, Brisbane, Queensland, Australia.
Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Natalie Bradford (N)

Cancer and Palliative Care Outcomes Centre at Centre for Children's Health Research, Queensland University of Technology, Brisbane, Queensland, Australia.

Jason D Pole (JD)

Centre for Health Services Research, The University of Queensland, Herston, Queensland, Australia.
The University of Toronto, Dalla Lana School of Public Health, Toronto, Ontario, Canada.

Classifications MeSH