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In a Letter to the Editor of the American Journal of Hematology, Salem Bahashwan and colleagues from Clermont Auvergne University, Clermont-Ferrand, France, reported data from their study which evaluated the efficacy and tolerance of gemtuzumab ozogamicin, intermediate-dose cytarabine, and mitoxantrone (MIDAM) as salvage therapy in patients with relapsed or refractory (R/R) acute myeloid leukemia (AML). The impact of post-remission therapy after MIDAM therapy was also evaluated.
Eighty-six patients (median age = 60 years; range: 17–75) with relapsed (n = 62) or refractory (n = 24) AML who were treated with MIDAM regimen between 2008 and 2013 at Clermont Auvergne University Hospital were included in this study. Patients received a MIDAM regimen consisting of gemtuzumab ozogamicin (9 mg/m2 on day 4), cytarabine (1 g/m2 every 12 hours on day 1–5), and mitoxantrone (12 mg/m2/d on day 1–3) as salvage therapy after one (n = 73) or more (n = 13) prior therapy lines.
Of the 54 patients with CR or CRp, post-remission therapy consisted of chemo-based approaches (chemotherapy only, n = 10; chemotherapy plus autologous transplantation, n = 3) and allogeneic hematopoietic stem cell transplantation (allo-HSCT, n = 29). Seven patients who underwent allo-HSCT received consolidation therapy prior to allo-HSCT.
This study represents the largest cohort of patients treated with MIDAM who have been analyzed. The findings of this study demonstrate that MIDAM regimen is a valid therapeutic option as salvage chemotherapy in patients with R/R AML and it is associated with an “acceptable toxicity profile.”
In addition, allo-HSCT was found to be the consolidation strategy of choice after MIDAM regimen and it is associated with no increased risk of VOD.
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