Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Since its approval in 2011, the Janus kinase 1/2 (JAK1/2) inhibitor ruxolitinib has evolved to become the centerpiece of therapy for myelofibrosis (MF), and its use in patients with hydroxyurea resistant or intolerant polycythemia vera (PV) is steadily increasing.
|
28500170 |
2017 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Selective JAK1 inhibition alone is unlikely to succeed in myelofibrosis.
|
28441920 |
2017 |
Primary Myelofibrosis
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In this open-label phase II study, we evaluated the efficacy and safety of three dose levels of INCB039110, a potent and selective oral JAK1 inhibitor, in patients with intermediate- or high-risk myelofibrosis and a platelet count ≥50×10<sup>9</sup>/L.
|
27789678 |
2017 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Purpose We evaluated the efficacy and safety of momelotinib, a potent and selective Janus kinase 1 and 2 inhibitor (JAKi), compared with ruxolitinib, in JAKi-naïve patients with myelofibrosis.
|
28930494 |
2017 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Janus kinase 1/2 (JAK1/2) inhibitor therapy is effective in alleviating myelofibrosis (MF)-related symptoms.
|
26659587 |
2016 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Ruxolitinib is a potent and specific JAK1/JAK2 inhibitor recently approved for the treatment of myelofibrosis.
|
25441108 |
2015 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
JAK1/2 inhibitors have broadened the therapeutic options in myelofibrosis.
|
25189727 |
2014 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
The JAK1/JAK2 inhibitor ruxolitinib produced significant reductions in splenomegaly and symptomatic burden and improved survival in patients with myelofibrosis (MF), irrespective of their JAK2 mutation status, in 2 phase III studies against placebo (COMFORT-I) and best available therapy (COMFORT-II).
|
24458439 |
2014 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Only one JAK1/JAK2 inhibitor has gained FDA approval for treatment of myelofibrosis.
|
24766055 |
2014 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
JAK2 inhibition became a reality with first patients receiving drugs that targeted JAK2 in 2007 and was marked by the first approval in 2011 of Ruxolitinib a JAK 1 and 2-inhibitor to treat myelofibrosis (MF).
|
25189729 |
2014 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
The in vitro treatment of splenic and peripheral blood MF CD34(+) cells with the JAK1/2/3 inhibitor, AZD1480, reduced the absolute number of CD34(+), CD34(+)CD90(+), and CD34(+)CXCR4(+) cells as well as assayable hematopoietic progenitor cells (HPCs) irrespective of the JAK2 and calreticulin mutational status.
|
25193869 |
2014 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Of these, the JAK1/2 inhibitor, ruxolitinib (INCB018424, Incyte Corporation) was recently approved for the treatment of patients with myelofibrosis (MF).
|
23670175 |
2013 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Ruxolitinib is a small-molecule inhibitor of JAK1 and JAK2 and recently became the first drug approved by the United States Food and Drug Administration for the treatment of symptomatic intermediate- or high-risk myelofibrosis.
|
23307549 |
2013 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Clinical trials demonstrated that JAK1/2 inhibitors ameliorate constitutional symptoms and reduce spleen size in patients with myelofibrosis.
|
23313046 |
2013 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Ruxolitinib is an oral JAK1 and JAK2 inhibitor that has recently been approved for the treatment of myelofibrosis and has been tested against other hematologic malignancies.
|
23406773 |
2013 |
Primary Myelofibrosis
|
0.100 |
Biomarker
|
disease |
BEFREE |
Ruxolitinib is the first JAK1/2 inhibitor approved by the Food and Drug Administration (FDA) for the treatment of patients with intermediate- or high-risk MF.
|
23042420 |
2012 |