Clinical impact of the CONUT score in patients with multiple myeloma.

Hidekazu Itamura, Shinya Kimura, Eisaburo Sueoka, Atsushi Kawaguchi, Kensuke Kojima, Toshihiko Ando, Yasushi Kubota, Takero Shindo, Masako Yokoo, Mariko Yoshimura, Sho Okamoto, Kazuharu Kamachi, Kyosuke Yamaguchi, Atsujiro Nishioka, Haruhiko Sano, Haruna Kizuka-Sano, Kana Kusaba, Keisuke Kidoguchi, Hiroshi Ureshino

Journal: Annals of hematology 2020;99(1):113-119

PMID: 31768678

Abstract

Novel anti-myeloma drugs have significantly improved the overall survival (OS) of patients with multiple myeloma (MM). However, not all MM patients treated with these drugs show survival benefits, and biologic and genetic prognostic factors are insufficient to predict the response to treatment. Decreasing treatment-related complications is important to improve the efficacy of treatment in patients with MM. The Controlling Nutritional Status (CONUT) score is a screening method for poor nutritional status, which is associated with poor prognosis in several cancers because it increases the rate of treatment-related complications. We retrospectively analyzed the OS of 64 patients with symptomatic MM and evaluated the correlation between the CONUT score and patient prognosis in MM. The median age at diagnosis was 66 years, and multivariate analysis showed that a high CONUT score (≥ 5; hazard ratio, 3.937; 95% confidence interval, 1.214-12.658; P = 0.022) was an independent prognostic risk factor. Subgroup analysis was performed according to patient age because the choice of treatment strategy, particularly autologous peripheral blood stem cell transplantation (auto-PBSCT), can vary depending on age in MM patients. Younger patients (< 65 years old) who received auto-PBSCT and had a lower CONUT score (0-3) showed a significantly better survival outcome than those with a higher CONUT score (≥ 4) (median OS, not reached vs. 64.1 months; P = 0.011). The CONUT score is simple to calculate and provides a useful prognostic indicator in patients with MM, especially transplant-eligible patients.

Address: Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan.; Department of Internal Medicine, Saga-ken Medical Centre Koseikan, Saga, Japan.; Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan. [email protected].; Department of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan. [email protected].; Department of Hematology and Oncology, Kyoto University Graduate School of Medicine, Kyoto, Japan.; Center for Comprehensive Community Medicine, Faculty of Medicine, Saga University, Saga, Japan.; Department of Clinical Laboratory Medicine, Faculty of Medicine, Saga University, Saga, Japan.; Department of Laboratory Medicine, Saga University Hospital, Saga, Japan.; Department of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.

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