Assessing Health-related Quality of Life in Sarcoma Patients

Sponsor
The Netherlands Cancer Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT04071704
Collaborator
Radboud University Medical Center (Other), Leiden University Medical Center (Other), Centre Leon Berard (Other), University Hospital Carl Gustav Carus (Other), Heidelberg University (Other), Johannes Gutenberg University Mainz (Other), Fondazione IRCCS Istituto Nazionale dei Tumori, Milano (Other), National Cancer Institute, Naples (Other), Maria Sklodowska-Curie National Research Institute of Oncology (Other), Hospital San Carlos, Madrid (Other), Royal Marsden NHS Foundation Trust (Other), Beatson West of Scotland Cancer Centre (Other), University Hospital Southampton NHS Foundation Trust (Other), Royal National Orthopaedic Hospital NHS Trust (Other), Bank of Cyprus Oncology Centre (Other), Institut Català d'Oncologia (Other), University of Adelaide (Other), King Hussein Cancer Center (Other), Oslo University Hospital (Other), Erasmus Medical Center (Other), University Medical Center Groningen (Other), Centre Oscar Lambret (Other), Aretaieio Hospital (Other), Hospital Universitario Fundación Jiménez Díaz (Other), The Christie NHS Foundation Trust (Other), Ain Shams University (Other), Prince of Wales Hospital, Shatin, Hong Kong (Other), Sheba Medical Center (Other)
689
3
47
229.7
4.9

Study Details

Study Description

Brief Summary

Although the clinical effectiveness of sarcoma treatment has improved, long-lasting and cumulative treatment side-effects may often detract from the overall marginal advantage. Information only on survival is insufficient to determine the net clinical benefit of a treatment. It is important to assess treatment effectiveness both in terms of objective outcomes (e.g., response, recurrence and survival) and in terms of subjective patient reported outcomes (PROs), objective functional outcomes including health-related quality of life (HRQoL).

Previous studies have predominantly used generic HRQoL instruments, which cover some relevant issues but do not capture all the unique experiences of patients with sarcoma, and thus lack content validity. A sarcoma-specific questionnaire should be able to detect, with more sensitivity, side-effects, symptoms and problems with function that are particularly relevant to patients with sarcoma. To date , there is no specific sarcoma HRQoL instrument available; and, given the heterogeneity of the disease in terms of subtype, location, age and treatment, the development of such an instrument may be challenging.

The aim of this collaborative project between the EORTC Quality of Life Group (QLG) and the EORTC Soft Tissue and Bone Sarcoma Group (STBSG) is to raise the standard of HRQoL measurement in patients with sarcoma. An important question remains to be answered: Is it possible to develop one PROs questionnaire covering HRQoL issues that are relevant to all adult patients with sarcoma, or are the HRQoL issues related to the different localization / treatment sufficiently different to warrant the creation of separate item lists selected from the EORTC QLG Item Library?

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The investigators will follow the EORTC QLG questionnaire development guidelines. First, a computerized search of the academic literature will be performed to identify all relevant HRQoL issues for and existing HRQoL questionnaires currently used among patients with sarcoma. In parallel, semi-structured interviews will be conducted worldwide with patients with sarcoma(N=179) and health care professionals (HCPs; N=35; phase 1a). The patient sample will be stratified to capture diversity across the sarcoma population tumour location (extremities, axial, head and neck, thorax, retroperitoneal/intra-abdominal and gynecological), stage (localized vs. metastatic disease ) and type or lines of treatment .

    This list of HRQoL issues generated by the a) literature search, b) relevant items from the Item Library, and c) semi-structured patient and HCP interviews, and will be consolidated into a comprehensive list of issues for all languages of collaborating countries.

    In phase 1b, the new list of HRQoL issues will be presented to another group of patients with sarcoma(N=475) and HCPs (N=72). Patients and HCPs will be asked to rate the HRQoL issues on relevance (4point Likert scale) and to prioritize the 10 most important issues.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    689 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Incorporating the Patient Voice in Sarcoma Research: How Can we Assess Health-related Quality of Life in This Heterogeneous Group of Patients?
    Actual Study Start Date :
    May 1, 2019
    Anticipated Primary Completion Date :
    Mar 31, 2023
    Anticipated Study Completion Date :
    Mar 31, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Patients

    Patients who have been or are being treated for sarcoma.

    Health care professionals

    Health care professionals with extensive experience in sarcoma care (medical oncologists, radiation oncologists, surgical oncologists, orthopaedic surgeons, nurse specialists, psychologists, physiotherapists)

    Outcome Measures

    Primary Outcome Measures

    1. a framework for a HRQoL measure for patients with sarcoma [1 week (and for several issues 4 weeks according to EORTC questionnaire guidelines)]

      the framework will outline which strategy to adopt for HRQoL in patients with sarcoma: the EORTC Quality of Life Questionnaire (QLQ)-C30 + one sarcoma module; EORTC QLQ-C30 + one sarcoma module + an item list; EORTC QLQ-C30 + item list. This will be based on analysis of the interview data (patients and HCPs) and the relevance of certain HRQoL rated by patients and health care professionals and possible identification of certain subgroups (according to tumour localization, type of sarcoma, disease stage and treatment).

    Secondary Outcome Measures

    1. an exhaustive list of all HRQoL issues relevant to sarcoma patients [1 week (and for several issues 4 weeks according to EORTC questionnaire guidelines)]

      based on a literature review, analysis of interviews with patients and health care professionals we will create an exhaustive list of all HRQoL issues relevant to sarcoma patients.

    2. the coverage of issues/items already available in the EORTC Item Library [1 week (and for several issues 4 weeks according to EORTC questionnaire guidelines)]

      the interview data and rating of HRQoL issues will be used to determine the overage of issues/ items in the EORTC Item Library and how the Item Library can be optimally used for the HRQoL measure for patients with sarcoma.

    3. the proportion of patients in subgroups rating issues/items as relevant [1 week (and for several issues 4 weeks according to EORTC questionnaire guidelines)]

      In order to determine if issues are sarcoma-generic or dependent of sarcoma localization, sarcoma subtype, disease stage or treatment we will analyze the proportion of patients in each subgroup rating HRQoL issues or items as relevant

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age at diagnosis 18 years or older

    • Having a confirmed diagnosis of sarcoma

    Exclusion Criteria:
    • Having any psychiatric condition or cognitive impairment that would hamper participation in interview/completion of self-reported questionnaires.

    • Patients with a Gastrointestinal Stroma Tumour (GIST) diagnosis, as they are quite unique in terms of type of disease and treatment.

    • Patients with Kaposi sarcoma, as this disease occurs quite often in people with AIDS

    • Patients with Carcinosarcoma as this disease is generally seen as a carcinoma

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital Carl Gustav Carus Dresden Germany
    2 Johannes Gutenberg University Mainz Mainz Germany
    3 Kiing Hussein Cancer Centre Amman Jordan

    Sponsors and Collaborators

    • The Netherlands Cancer Institute
    • Radboud University Medical Center
    • Leiden University Medical Center
    • Centre Leon Berard
    • University Hospital Carl Gustav Carus
    • Heidelberg University
    • Johannes Gutenberg University Mainz
    • Fondazione IRCCS Istituto Nazionale dei Tumori, Milano
    • National Cancer Institute, Naples
    • Maria Sklodowska-Curie National Research Institute of Oncology
    • Hospital San Carlos, Madrid
    • Royal Marsden NHS Foundation Trust
    • Beatson West of Scotland Cancer Centre
    • University Hospital Southampton NHS Foundation Trust
    • Royal National Orthopaedic Hospital NHS Trust
    • Bank of Cyprus Oncology Centre
    • Institut Català d'Oncologia
    • University of Adelaide
    • King Hussein Cancer Center
    • Oslo University Hospital
    • Erasmus Medical Center
    • University Medical Center Groningen
    • Centre Oscar Lambret
    • Aretaieio Hospital
    • Hospital Universitario Fundación Jiménez Díaz
    • The Christie NHS Foundation Trust
    • Ain Shams University
    • Prince of Wales Hospital, Shatin, Hong Kong
    • Sheba Medical Center

    Investigators

    • Principal Investigator: Olga Husson, PhD, The Netherlands Cancer Institute
    • Principal Investigator: Winette van der Graaf, PhD, MD, The Netherlands Cancer Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    The Netherlands Cancer Institute
    ClinicalTrials.gov Identifier:
    NCT04071704
    Other Study ID Numbers:
    • EORTC-1749
    First Posted:
    Aug 28, 2019
    Last Update Posted:
    Jan 6, 2022
    Last Verified:
    Dec 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by The Netherlands Cancer Institute
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 6, 2022