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Quality of Life of Patients With Osteosarcoma in the European American Osteosarcoma Study-1 (EURAMOS-1): Development and Implementation of a Questionnaire Substudy.
Calaminus, Gabriele; Jenney, Meriel; Hjorth, Lars; Baust, Katja; Bernstein, Mark; Bielack, Stefan; Vos, Patricia De; Hogendoorn, Pancras C W; Jovic, Gordana; Krailo, Mark; Kreitz, Kiana; Marina, Neyssa; Popoola, Babasola O; Sauerland, Cristina; Smeland, Sigbjørn; Teske, Carmen; Schweinitz, Clara V; Whelan, Jeremy; Wiener, Andreas; Sydes, Matthew R; Nagarajan, Rajaram.
Afiliação
  • Calaminus G; Department of Pediatric Hematology and Oncology, University Hospital Bonn, Bonn, Germany.
  • Jenney M; Children & Women's Services Clinical Board, University Hospital of Wales, Cardiff, United Kingdom.
  • Hjorth L; Pediatrics, Department of Clinical Sciences Lund, Skane University Hospital, Lund University, Lund, Sweden.
  • Baust K; Department of Pediatric Hematology and Oncology, University Hospital Bonn, Bonn, Germany.
  • Bernstein M; IWK Health Centre, Dalhousie University, Halifax, NS, Canada.
  • Bielack S; Cooperative Osteosarcoma Study Group, Klinikum Stuttgart - Olgahospital, Stuttgart, Germany.
  • Vos P; Department of Pediatric Hematology and Oncology, Gent University Hospital, Gent, Belgium.
  • Hogendoorn PCW; Department of Pathology, Leiden University Medical Center, Leiden, Netherlands.
  • Jovic G; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, University College London, London, United Kingdom.
  • Krailo M; Department of Preventive Medicine, Keck Medical Center at the University of Southern California, Los Angeles, CA, United States.
  • Kreitz K; Children's Oncolgy Group, Arcadia, CA, United States.
  • Marina N; Institute of Biostatistics and Clinical Research, University of Muenster, Muenster, Germany.
  • Popoola BO; Five Prime Therapeutics Inc, South San Francisco, CA, United States.
  • Sauerland C; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, University College London, London, United Kingdom.
  • Smeland S; Institute of Biostatistics and Clinical Research, University of Muenster, Muenster, Germany.
  • Teske C; Division of Cancer Medicine and Scandinavian Sarcoma Group, Oslo University Hospital, Oslo, Norway.
  • Schweinitz CV; Institute for Clinical Medicine, University of Oslo, Oslo, Norway.
  • Whelan J; Department of Pediatric Hematology and Oncology, University Hospital Bonn, Bonn, Germany.
  • Wiener A; Department of Pediatric Hematology and Oncology, University Hospital Bonn, Bonn, Germany.
  • Sydes MR; Department of Oncology, University College Hospital, London, United Kingdom.
  • Nagarajan R; West German Proton Therapy Centre Essen, Essen, Germany.
JMIR Res Protoc ; 8(8): e14406, 2019 Sep 26.
Article em En | MEDLINE | ID: mdl-31573951
ABSTRACT

BACKGROUND:

The quality of life (QoL) of patients with osteosarcoma (OS) may be adversely affected by the disease or its treatment. Therefore, it is important to understand the QoL of patients undergoing treatment for OS to improve the QoL. We report on the first prospective international QoL study that was embedded within a large randomized clinical trial from 4 national study groups.

OBJECTIVE:

This paper aimed to describe the QoL study development, methodology, accrual details, and characteristics of the QoL cohort.

METHODS:

A total of 2260 patients registered in the EURopean AMerican Osteosarcoma Study-1 (EURAMOS-1), of whom 97.92% (2213/2260) were eligible for the optional QoL assessment and could participate in terms of questionnaire availability. Overall, 61.86% (1369/2213) of patients and/or proxies completed the QoL evaluation at the first assessment time point (E1) after the start of preoperative treatment. The QoL measures used (self- and/or proxy reports) depending on the patient's age and national study group. Participants and nonparticipants in the ancillary QoL study were compared regarding relevant demographic and disease-related characteristics at registration in the trial.

RESULTS:

The participation rate at time point E1 did not differ with regard to age, gender, the occurrence of pathological fracture, or the presence of any metastases at diagnosis. No differences were found regarding the primary tumor site. Only the national study group affiliation had an influence on participation. Participation decreased linearly with trial progress up to 20% at the final time point of QoL assessment.

CONCLUSIONS:

This study demonstrates the feasibility of international cooperation for the purpose of assessing and understanding the QoL of pediatric and adolescent/young adult patients with cancer. Future outcomes of this QoL substudy will help to adapt interventions to improve QoL.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2019 Tipo de documento: Article