Hypoxia-Inducible Factor-Prolyl-Hydroxylase and Sodium-Glucose Cotransporter 2 Inhibitors for Low-Risk Myelodysplastic Syndrome-Related Anemia in Patients with Chronic Kidney Disease: A Report of Three Cases.
Hypoxia-Inducible Factor-Prolyl-Hydroxylase and Sodium-Glucose Cotransporter 2 Inhibitors for Low-Risk Myelodysplastic Syndrome-Related Anemia in Patients with Chronic Kidney Disease: A Report of Three Cases.
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DOI:
10.3390/hematolrep15010019
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发表时间:
2023-03-06
影响因子:
0.9
通讯作者:
Horiuchi, Takahiko
中科院分区:
文献类型:
--
作者:
Yamasaki, Satoshi;Horiuchi, Takahiko
关键词:
Although daprodustat, a hypoxia-inducible factor prolyl hydroxylase inhibitor, and dapagliflozin, a sodium-glucose cotransporter 2 inhibitor, have been approved for the treatment of renal anemia in Japan, their efficacy and safety for patients aged 80 years or older with low-risk myelodysplastic syndrome (MDS)-related anemia have not been demonstrated. Our case series comprised two men and one woman aged >80 years with low-risk MDS-related anemia and diabetic mellitus (DM)-related chronic kidney disease who were dependent on red blood cell transfusions and in whom erythropoiesis-stimulating agents had been insufficient. All three patients received daprodustat and additional dapagliflozin achieved red blood cell transfusion independence and were followed up for >6 months. Daily oral daprodustat was well tolerated. There were no fatalities or progression to acute myeloid leukemia during the >6-month follow-up after daprodustat initiation. On the basis of these outcomes, we consider 24 mg of daprodustat combined with 10 mg of dapagliflozin daily an effective form of treatment for low-risk MDS-related anemia. Further studies are required to clarify the synergistic effects of daprodustat and dapagliflozin, which correct chronic kidney disease-related anemia by promoting endogenous erythropoietin production and normalizing iron metabolism to manage low-risk MDS in the long term.
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影响因子:
11.4
作者:
通讯作者:
--
DOI:
10.1084/jem.20201544
发表时间:
2021-07-05
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Trowbridge JJ;Starczynowski DT
通讯作者:
Starczynowski DT
影响因子:
12.8
作者:
Steensma DP
通讯作者:
Steensma DP
影响因子:
3.2
作者:
Kurata, Yu;Nangaku, Masaomi
通讯作者:
Nangaku, Masaomi
DOI:
10.1124/jpet.117.242503
发表时间:
2017-12-01
影响因子:
3.5
作者:
Ariazi, Jennifer L.;Duffy, Kevin J.;Erickson-Miller, Connie
通讯作者:
Erickson-Miller, Connie