2021
A Randomized Open-Label, Phase 3 Study to Evaluate Imetelstat Versus Best Available Therapy (BAT) in Patients with Intermediate-2 (Int-2) or High-Risk Myelofibrosis (MF) Refractory to Janus Kinase Inhibitor (JAKi)
Abstract: MF is a life-threatening myeloproliferative neoplasm. The JAKi ruxolitinib and fedratinib are the only FDA approved treatment options for MF. Despite benefits reported with ruxolitinib in the front-line setting, a high proportion of patients (pts) discontinue treatment (Abdelrahman 2015), and the median overall survival (OS) is 13-16 months (Kuykendall 2018; Newberry 2017; Schain 2019; Palandri 2019; Mcnamara 2019), highlighting a great unmet need for pts non-responsive to a JAKi treatment. Imet…
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“…However, treatment with imetelstat was associated with grade 3 or higher neutropenia (in 68%) and thrombocytopenia (in 62%) [85]. Recently, in 2024, imetelstat received FDA approval for LR-MDS, relapsed or refractory to ESAs, while investigations are ongoing in MF [86,87].…”
Section: Imetelstat
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confidence: 99%