Myelofibrosis
F Passamonti, B Mora - Blood, 2023 - ashpublications.org
The clinical phenotype of primary and post–polycythemia vera and postessential
thrombocythemia myelofibrosis (MF) is dominated by splenomegaly, symptomatology, a …
thrombocythemia myelofibrosis (MF) is dominated by splenomegaly, symptomatology, a …
Telomerase-targeted therapies in myeloid malignancies
Human telomeres are tandem arrays that are predominantly composed of 5′-TTAGGG-3′
nucleotide sequences at the terminal ends of chromosomes. These sequences serve 2 …
nucleotide sequences at the terminal ends of chromosomes. These sequences serve 2 …
Addition of navitoclax to ongoing ruxolitinib therapy for patients with myelofibrosis with progression or suboptimal response: phase II safety and efficacy
CN Harrison, JS Garcia, TCP Somervaille… - Journal of Clinical …, 2022 - ascopubs.org
PURPOSE Targeting the BCL-XL pathway has demonstrated the ability to overcome Janus
kinase inhibitor resistance in preclinical models. This phase II trial investigated the efficacy …
kinase inhibitor resistance in preclinical models. This phase II trial investigated the efficacy …
Momelotinib versus danazol in symptomatic patients with anaemia and myelofibrosis (MOMENTUM): results from an international, double-blind, randomised …
S Verstovsek, AT Gerds, AM Vannucchi, HK Al-Ali… - The Lancet, 2023 - thelancet.com
Background Janus kinase (JAK) inhibitors approved for myelofibrosis provide spleen and
symptom improvements but do not meaningfully improve anaemia. Momelotinib, a first-in …
symptom improvements but do not meaningfully improve anaemia. Momelotinib, a first-in …
MANIFEST: pelabresib in combination with ruxolitinib for Janus kinase inhibitor treatment-naive myelofibrosis
J Mascarenhas, M Kremyanskaya… - Journal of Clinical …, 2023 - ascopubs.org
PURPOSE Standard therapy for myelofibrosis comprises Janus kinase inhibitors (JAKis), yet
spleen response rates of 30%-40%, high discontinuation rates, and a lack of disease …
spleen response rates of 30%-40%, high discontinuation rates, and a lack of disease …
Randomized, single-blind, multicenter phase II study of two doses of imetelstat in relapsed or refractory myelofibrosis
J Mascarenhas, RS Komrokji, F Palandri… - Journal of Clinical …, 2021 - ascopubs.org
PURPOSE Patients with myelofibrosis who are relapsed or refractory (R/R) to Janus-
associated kinase inhibitors (JAKis) have poor clinical outcomes including dismal overall …
associated kinase inhibitors (JAKis) have poor clinical outcomes including dismal overall …
Fedratinib in patients with myelofibrosis previously treated with ruxolitinib: an updated analysis of the JAKARTA2 study using stringent criteria for ruxolitinib failure
CN Harrison, N Schaap, AM Vannucchi… - American journal of …, 2020 - Wiley Online Library
Fedratinib is an oral, selective Janus kinase 2 (JAK2) inhibitor. The phase II JAKARTA2
study assessed fedratinib in patients with intermediate‐or high‐risk myelofibrosis (MF) who …
study assessed fedratinib in patients with intermediate‐or high‐risk myelofibrosis (MF) who …
A prognostic model to predict survival after 6 months of ruxolitinib in patients with myelofibrosis
Ruxolitinib (RUX) is extensively used in myelofibrosis (MF). Despite its early efficacy, most
patients lose response over time and, after discontinuation, have a worse overall survival …
patients lose response over time and, after discontinuation, have a worse overall survival …
Overall survival in the SIMPLIFY-1 and SIMPLIFY-2 phase 3 trials of momelotinib in patients with myelofibrosis
Janus kinase inhibitors (JAKi) approved for myelofibrosis provide spleen and symptom
improvements but do not address anemia, a negative prognostic factor. Momelotinib, an …
improvements but do not address anemia, a negative prognostic factor. Momelotinib, an …
Addition of navitoclax to ongoing ruxolitinib treatment in patients with myelofibrosis (REFINE): a post-hoc analysis of molecular biomarkers in a phase 2 study
N Pemmaraju, JS Garcia, J Potluri, JG Harb… - The Lancet …, 2022 - thelancet.com
Background Primary analyses of cohort 1a of the REFINE trial showed that addition of
navitoclax to ruxolitinib induced a 35% or greater reduction in spleen volume (SVR 35) and …
navitoclax to ruxolitinib induced a 35% or greater reduction in spleen volume (SVR 35) and …