Redefining chemotherapy-induced peripheral neuropathy through symptom cluster analysis and patient-reported outcome data over time.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
27 Nov 2019
Historique:
received: 12 03 2019
accepted: 11 11 2019
entrez: 29 11 2019
pubmed: 30 11 2019
medline: 4 4 2020
Statut: epublish

Résumé

Chemotherapy-induced peripheral neuropathy (CIPN) is common among cancer patients treated with neurotoxic chemotherapy agents. Better knowledge on symptom clusters of CIPN may help improve symptom management in clinical practice. This study aimed to identify symptom clusters of CIPN and to map their trajectories before initiation of chemotherapy to 12-month follow-up. A secondary analysis of a longitudinal dataset was conducted using principal component approach. The European Organization for the Research and Treatment of Cancer Quality of Life Questionnaires Core 30 and CIPN 20 were used to measure symptom clusters of CIPN in patients with mixed cancer diagnosis across 10 time points over 12 months. Sample size in each assessment point ranged from 118 to 343 participants. Four CIPN symptom clusters were identified, including a clear sensory neuropathy symptom cluster, a mixed motor-sensory neuropathy symptom cluster, a mixed sensorimotor neuropathy symptom cluster, and a less clear autonomic neuropathy symptom cluster. The core symptoms in each symptom cluster were mostly stable while the secondary symptoms changed over time. The analysis suggests that CIPN is predominantly a sensory neuropathy with no evidence of a pure motor dysfunction but with mixed motor-related and autonomic changes accompanying sensory dysfunctions over time. Future symptom management strategies can be designed based on the morphology of CIPN.

Sections du résumé

BACKGROUND BACKGROUND
Chemotherapy-induced peripheral neuropathy (CIPN) is common among cancer patients treated with neurotoxic chemotherapy agents. Better knowledge on symptom clusters of CIPN may help improve symptom management in clinical practice. This study aimed to identify symptom clusters of CIPN and to map their trajectories before initiation of chemotherapy to 12-month follow-up.
METHODS METHODS
A secondary analysis of a longitudinal dataset was conducted using principal component approach. The European Organization for the Research and Treatment of Cancer Quality of Life Questionnaires Core 30 and CIPN 20 were used to measure symptom clusters of CIPN in patients with mixed cancer diagnosis across 10 time points over 12 months.
RESULTS RESULTS
Sample size in each assessment point ranged from 118 to 343 participants. Four CIPN symptom clusters were identified, including a clear sensory neuropathy symptom cluster, a mixed motor-sensory neuropathy symptom cluster, a mixed sensorimotor neuropathy symptom cluster, and a less clear autonomic neuropathy symptom cluster. The core symptoms in each symptom cluster were mostly stable while the secondary symptoms changed over time.
CONCLUSIONS CONCLUSIONS
The analysis suggests that CIPN is predominantly a sensory neuropathy with no evidence of a pure motor dysfunction but with mixed motor-related and autonomic changes accompanying sensory dysfunctions over time. Future symptom management strategies can be designed based on the morphology of CIPN.

Identifiants

pubmed: 31775665
doi: 10.1186/s12885-019-6352-3
pii: 10.1186/s12885-019-6352-3
pmc: PMC6882224
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1151

Subventions

Organisme : This study was supported by a Polytechnic University Direct grant (in HK) and an NCIS Seed Funding Grant, National Medical Research Council (Singapore).
ID : n/a

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Auteurs

Mian Wang (M)

School of Nursing, The Hong Kong Polytechnic University, Hong Kong, Hong Kong SAR.

Hui Lin Cheng (HL)

School of Nursing, The Hong Kong Polytechnic University, Hong Kong, Hong Kong SAR.

Violeta Lopez (V)

Alice Lee Centre for Nursing Studies, National University of Singapore, Singapore, Singapore.

Raghav Sundar (R)

The N.1 Institute of Health, National University of Singapore, Singapore, Singapore.

Janelle Yorke (J)

Division of Nursing, Midwifery & Social Work, University of Manchester, Manchester, UK.
Christie Patient Centred Research (CPCR), The Christie NHS Foundation Trust, Manchester, UK.

Alex Molassiotis (A)

School of Nursing, The Hong Kong Polytechnic University, Hong Kong, Hong Kong SAR. alex.molasiotis@polyu.edu.hk.

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