Potential Biomarker, Drug Target ID’d for Adult Leukemia
Tumors from adults with B-cell precursor acute lymphoblastic leukemia have epigenetic changes.
Tumors from adults with B-cell precursor acute lymphoblastic leukemia have epigenetic changes.
Teva Pharmaceuticals announced that the FDA has approved Synribo (omacetaxine mepesuccinate) for Injection to treat adult patients with chronic phase (CP) or accelerated phase (AP) chronic myeloid leukemia (CML) with resistance and/or intolerance to two or more tyrosine kinase inhibitors (TKIs).
AML patients whose peripheral blasts clear six days or less after chemotherapy have better survival
ARIAD Pharmaceuticals announced that the FDA has accepted for filing the New Drug Application (NDA) of ponatinib for patients with resistant or intolerant chronic myeloid leukemia (CML) or Philadelphia-chromosome positive acute lymphoblastic leukemia (Ph+ ALL); the FDA also has granted ARIAD’s request for Priority Review.
The longer a child is fed formula and the later the age solid foods are introduced, the greater the risk for developing acute lymphoblastic leukemia.
A new profiling technique determines acute myeloid leukemia (AML) cells’ “readiness” for apoptotic cell death – and hence, their likely responses to chemotherapy.
Treating patients with chronic lymphocytic leukemia (CLL) with a proprietary extract of Panax quinquefolius, CVT-E002, resulted in a trend toward reduced rates of moderate to severe acute respiratory illness (ARI); however, the agent did not significantly reduce ARI days or antibiotic use.
Information provided by BH3 profiling, an assay of mitochondrial apoptotic function, can “potentially be exploited” to personalize therapy for patients with acute myelogenous leukemia.
In HIV-positive patients with Hodgkin lymphoma treated with ABVD chemotherapy, despite more extensive disease, worse prognosis but not worse outcome.
Survivors of Hodgkin lymphoma had significantly fewer children after treatment than matched population controls.