Through 2018, five new drugs will launch for the treatment of myelodysplastic syndromes (MDS), three of which are expected to offer much-needed second-line therapeutic options in the hypomethylating agent (HMA)-refractory higher-risk MDS population, according to a new report from health care advisory firm Decision Resources.
Currently, there is only one curative treatment for MDS - allogeneic hematopoietic stem cell transplant (HSCT). However, old age and poor general performance status classifies approximately 75% of patients as ineligible for this treatment.
Between 2004 and 2006, the US MDS market expanded when the first drug therapy options were approved for the indication - azacitidine (Celgene’s Vidaza), lenalidomide (Celgene’s Revlimid) and decitabine (Eisai/MGI Pharma’s Dacogen). No new therapies have been approved in the USA for MDS since 2006; only azacitidine has been approved for MDS in Europe, although experts believe an EU approval for lenalidomide is imminent.
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