Impact of Skeletal Muscle Depletion on Patients with Myelodysplastic Syndrome Treated with Azacitidine

Author:

Takada Eri1,Nakamura Nobuhiko2ORCID,Kaneda Yuto2,Fukuno Kenji3,Lee Shin4,Fujita Kei4,Morishita Tetsuji4,Ikoma Yoshikazu2,Matsumoto Takuro2,Nakamura Hiroshi2,Kitagawa Junichi5,Kanemura Nobuhiro2ORCID,Kasahara Senji5,Hara Takeshi4,Tsurumi Hisashi24,Shimizu Masahito2

Affiliation:

1. Department of Hematology, Gifu-Seino Medical Center, Ibi Kosei Hospital, Gifu 501-0619, Japan

2. Department of Hematology and Infectious Disease, Gifu University Hospital, Gifu 501-1194, Japan

3. Department of Hematology, Takayama Red Cross Hospital, Gifu 506-8550, Japan

4. Department of Hematology, Matsunami General Hospital, Gifu 501-6062, Japan

5. Department of Hematology, Gifu Municipal Hospital, Gifu 500-8513, Japan

Abstract

Background: Azacitidine (AZA) is the standard treatment for patients with high-risk myelodysplastic syndromes (MDS). The impact of skeletal muscle depletion (SMD), which is associated with outcomes of hematological malignancies, on the clinical course of MDS patients treated with AZA was investigated. Methods: This retrospective, observational study included 50 MDS patients treated with AZA. Muscle mass was evaluated using the skeletal muscle index (SMI), which is the area of muscle mass at the third lumbar vertebra on CT images divided by the square of the height. Results: Of the enrolled patients, 39 were males, and their median age was 69.5 years. Twenty-seven (20 male and 7 female) patients showed SMD. The median survival was 13.4 months in the SMD group and 15.2 months in the non-SMD group, with no significant difference and no significant association between the response rate or severe non-hematological toxicities and the presence of SMD. By contrast, grade 3–4 anemia and thrombocytopenia were significantly more frequent in the SMD group than in the non-SMD group. SMD was associated with severe anemia and thrombocytopenia in MDS patients treated with AZA. Conclusion: Reduced skeletal muscle mass may predict severe hematological toxicity in MDS patients treated with AZA.

Publisher

MDPI AG

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