Quality-of-Life Assessment in Pediatric Advanced Cancer: Development of the Patient-Reported Outcome Measure Advance QoL

Author:

Robichaud Lye-Ann12ORCID,Felipe Julie1,Duval Michel34,Michon Bruno5,Olivier-D’Avignon Marianne6,Perreault Sébastien27,Tyo-Gomez Mathias8,Marquis Marc-Antoine39ORCID,Sultan Serge123ORCID

Affiliation:

1. Department of Psychology, Université de Montréal, Montréal, QC H3C 3J7, Canada

2. Azrieli Research Centre, CHU Sainte-Justine, Montréal, QC H3T 1C5, Canada

3. Department of Pediatrics, Université de Montréal, Montréal, QC H3C 3J7, Canada

4. Department of Hematology-Oncology, CHU Sainte-Justine, Montréal, QC H3T 1C5, Canada

5. Centre Mère-Enfant Soleil, CHU de Québec-Université Laval, Québec, QC G1V 4G2, Canada

6. School of Social Work, Université Laval, Québec, QC G1V 0A6, Canada

7. Department of Neurology, CHU Sainte-Justine, Montréal, QC H3T 1C5, Canada

8. Psycho-Oncology Center (CPO), CHU Sainte-Justine, Montreal, QC H3T 1C5, Canada

9. Department of General Pediatrics, CHU Sainte-Justine, Montréal, QC H3T 1C5, Canada

Abstract

A recent measure was developed to assess the Quality of Life (QoL) of young people with advanced cancer and is available for parents and professionals (Advance QoL). The present study aimed to elaborate self-reported versions for children and adolescents with advanced cancer. We adopted a four-phase research plan: (1) to elaborate the Advance QoL questionnaire for youth (8–12 and 13–18 years old) with a team of young research partners; (2) to evaluate the understandability of these versions in a sample of 12 young patients from the target population using cognitive interviews; (3) to assess social validity in the same group using a questionnaire and the content validity index (CVI); and (4) to refine the questionnaires according to these results. Four major themes were identified: (1) issues affecting the understanding of the tool; (2) issues that did not affect the understanding of the tool; (3) modifications to improve the tool; and (4) positive features of the tool. Advance QoL was well received, and feedback was positive. Adjustments were made according to young people’s comments and two self-reported versions are now available. It is essential to measure the key domains of QoL in advanced cancer. Advance QoL self-report versions will help target the specific needs of young people with this condition and their families.

Funder

Canadian Institutes of Health Research

Fondation du CHU Sainte-Justine

Réseau québécois de recherche en soins palliatifs et de fin de vie

Coast-to-Coast Canada Foundation

Publisher

MDPI AG

Reference50 articles.

1. American Cancer Society (2021, November 19). Cancer in Children. Available online: https://canceratlas.cancer.org/the-burden/cancer-in-children/.

2. Comité Consultatif des Statistiques Canadiennes sur le Cancer, Société Canadienne du Cancer, and Statistique Canada et l’Agence de la Santé Publique du Canada (2021). Statistiques Canadiennes sur le Cancer 2021, Société Canadienne du Cancer.

3. Global childhood cancer survival estimates and priority-setting: A simulation-based analysis;Ward;Lancet Oncol.,2019

4. Research Priorities in Pediatric Palliative Care;Baker;J. Pediatr.,2015

5. Mongeau, S., Champagne, M., and Lussier, L. (2014). Le Soutien aux Familles D‘enfants Gravement Malades: Regards sur des Pratiques Novatrices, Presses de l‘Université du Québec. Collection Problèmes Sociaux et Interventions Sociales.

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