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.
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S.K. received research funding from Celgene, Janssen, Bristol-Myers Squibb, Novartis, Takeda Pharmaceutical Co., LTD, and Ono Pharmaceutical Co., LTD; K.K. has sponsored research agreements with Janssen Research and Development; T.S. received research funding from Celgene. The other authors declare no conflicts of interest.
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Okamoto, S., Ureshino, H., Kidoguchi, K. et al. Clinical impact of the CONUT score in patients with multiple myeloma. Ann Hematol 99, 113–119 (2020). https://doi.org/10.1007/s00277-019-03844-2
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DOI: https://doi.org/10.1007/s00277-019-03844-2