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Merck

A promising immunosuppressive strategy of cyclosporine alternately combined with levamisole is highly effective for moderate aplastic anemia.

Annals of hematology (2013-04-27)
Xingxin Li, Yingqi Shao, Meili Ge, Jun Shi, Jinbo Huang, Zhendong Huang, Jing Zhang, Neng Nie, Yizhou Zheng
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The appropriate management of patients with moderate aplastic anemia (mAA) remains to be unclear and controversial. A cohort of 118 patients with mAA received a novel immunosuppressive strategy of cyclosporine alternately combined with levamisole (CSA and LMS regimen), which included 42 newly diagnosed and 76 chronic (disease duration >6 months) cases. CSA and LMS regimen was orally administrated with the initial dose of CSA 3 mg/kg per day in adults or 5 mg/kg per day in children, and LMS 150 mg per day in adults or 2.5 mg/kg per day in children, continued for 12 more months after achieving maximal hematologic response, followed by a slow tapering. The overall response rates were of 100 and 86.8 % for newly diagnosed and chronic group, respectively. The 24-month progression-free survival were 95.2 % (95 % confidence intervals [CI], 85.9-100 %) and 93.6 % (95 % CI, 86.9-100 %) for newly diagnosed and chronic group, respectively (P = 0.50). The 2-year event-free survival for the patients in newly diagnosed group (86.6 %; 95 % CI, 70.4-100 %) was superior to that in chronic group (57.0 %; 95 % CI, 43.5-70.4 %, P = 0.001). To date, 11 patients relapsed and no patients evolved to clonal disorders. Thus, CSA and LMS regimen represents a promising immunosuppressive strategy for mAA.

MATERIALS
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Supelco
Levamisol hydrochloride, VETRANALยฎ, analytical standard
Levamisole hydrochloride for system suitability, European Pharmacopoeia (EP) Reference Standard
Levamisole hydrochloride, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
(โˆ’)-Tetramisole hydrochloride, ≥99% (GC)