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. 2018 Mar 27;18(1):350.
doi: 10.1186/s12885-018-4293-x.

Quality of life of survivors of malignant pleural mesothelioma in Japan: a cross sectional study

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Quality of life of survivors of malignant pleural mesothelioma in Japan: a cross sectional study

Yasuko Nagamatsu et al. BMC Cancer. .

Abstract

Background: Previous studies have indicated that people with malignant pleural mesothelioma (MPM) have a poor quality of life (QOL); however, information about the QOL of people with MPM in Japan is anecdotal. The aims of this study were to investigate the QOL of survivors of MPM in Japan and to determine the factors that correlate with their QOL.

Methods: This was a cross sectional study. The included patients were those diagnosed with MPM in Japan. We created a self-administered questionnaire consisting of 64 questions. The questionnaires were sent to hospitals and patient advocacy groups, distributed to the patients, completed, and sent back to the researchers by postal mail. QOL was assessed with the European Organization for Research and Treatment of Cancer 16 questionnaire (QLQ) and the short version of the core domains of the Comprehensive Quality of Life Outcome questionnaire (CoQoLo).

Results: In total, 133 questionnaires were collected. The QLQ assessments demonstrated that the survivors of MPM most frequently complained of fatigue, pain, sleep disturbances, and dyspnea. The symptom scales were acceptable, but the functional scales were significantly poorer for the patients with poor performance statuses (PSs). The short CoQoLo assessment was very unfavorable for 'Being free from physical pain.' Being a long-term survivor and a survivor with a poor PS were significantly correlated with poor global health status.

Conclusions: Survivors of MPM have impaired function, a variety of symptoms, and lower QOL. Survivors of MPM, even those in good physical condition, need broad support.

Keywords: Asbestos; CoQoLo; Mesothelioma; Palliative care; Quality of life; Questionnaire.

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Conflict of interest statement

Ethics approval and consent to participate

This study was approved by the institutional review board of Okayama Rosai Hospital (approval no. 2017–22). This study was also approved by the institutional review board of each hospital or institution that distributed the questionnaire to their patients according to their policy. The study was conducted based on the ethical principles of avoiding harm, voluntary participation, anonymity, and protection of privacy and personal information. The purpose, procedures, and confidentiality of the study were explained in written format. The participants were informed that nonparticipation would not disadvantage them. Return of the answered questionnaire was considered to constitute the patient’s consent.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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