Symptoms and health-related quality of life in patients with newly diagnosed multiple myeloma: a multicenter prospective cohort study

Author:

Suzuki Nana123ORCID,Okuyama Toru4,Akechi Tatsuo12,Kusumoto Shigeru3,Ri Masaki3,Inagaki Atsushi5,Kayukawa Satoshi6,Yano Hiroki7,Yoshida Takashi6,Shiraga Kazuhide3,Hashimoto Hiroya8,Aiki Sayo9,Iida Shinsuke3

Affiliation:

1. Department of Psychiatry and Cognitive-Behavioral Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan

2. Division of Psycho-Oncology and Palliative Care, Nagoya City University Hospital, Nagoya, Japan

3. Department of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan

4. Department of Psychiatry, Nagoya City University West Medical Center, Nagoya, Japan

5. Department of Hematology and Oncology, Nagoya City West Medical Center, Nagoya, Japan

6. Department of Hematology and Oncology, Nagoya Memorial Hospital, Nagoya, Japan

7. Department of Hematology, Kainan Hospital, Yatomi, Japan

8. Core Laboratory, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan

9. Department of Palliative Care, National Hospital Organization Osaka National Hospital, Osaka, Japan

Abstract

Abstract Objective Existing cross-sectional observational studies indicate that patients with multiple myeloma experience negative physical and psychological symptoms and low health-related quality of life. The study aim was to determine symptom prevalence, health-related quality of life and symptoms associated with health-related quality of life in patients with newly diagnosed multiple myeloma. Methods This multicenter longitudinal cohort study was conducted in four hospitals in Japan. Patients with newly diagnosed multiple myeloma were asked to report their symptom intensity and health-related quality of life using validated questionnaires at three points: at diagnosis (T1), 1 month (T2) and 12 months after diagnosis (T3). Symptoms associated with health-related quality of life were explored using a mixed-effects model. Results A total of 106 patients completed the assessment at T1. The symptoms more than 30% of patients reported were pain, disturbed sleep and distress at T1, pain, dry mouth, disturbed sleep and fatigue at T2, fatigue, numbness of tingling and pain and numbness or tingling at T3. Pain and depression were significantly associated with health-related quality of life negatively. Conclusions The finding suggests that more than 30% of multiple myeloma patients suffered from pain and various symptoms and they received suboptimal palliative care within a year after starting initial chemotherapy. Pain and depression should be the main targets of interventions to improve health-related quality of life in this population.

Funder

Cancer Research from the Ministry of Health, Labour and Welfare

Japanese Society for the Promotion of Science

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

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