July 28th 2025
Following the lifting of a clinical hold, the FDA has again accepted the BLA for tabelecleucel in adult and pediatric patients with EBV-positive PTLD.
Researchers Identify an Underlying Cause of Some Myelomas Associated With Gaucher Disease
February 12th 2016Researchers have uncovered the mechanism that causes about one-third of myeloma cases associated with Gaucher disease, showing that myeloma cells target certain lipids that are elevated in the blood of a subset of patients.
Age, Gender Among Factors Associated With Depression and Fatigue After HCT
February 11th 2016A number of clinical and sociodemographic factors, including age and gender, were found to be independently associated with fatigue and depression among cancer patients who were treated with hematopoietic cell transplantation.
MTSS1 Protein May Act As Tumor Suppressor, Downregulated in CML
January 29th 2016Laboratory studies of mice and human cells found that a protein called Metastasis suppressor 1 (Mtss1) is downregulated in hematopoietic and progenitor cells when chronic myeloid leukemia is present. Mtss1 levels are restored when complete remission is achieved, suggesting the pathway might represent a new therapeutic target.
FDA Expands Label for Carfilzomib in Multiple Myeloma
January 25th 2016The FDA recently expanded the drug label for carfilzomib (Kyprolis), which is now approved in combination with dexamethasone or with lenalidomide plus dexamethasone for patients with relapsed or refractory disease who have received one to three lines of therapy.
Pioglitazone, Other TZDs May Add Benefit to TKI Therapy in CML
January 11th 2016A laboratory study showed that peroxisome proliferator-activated receptor gamma agonists such as pioglitazone could help treat chronic myeloid leukemia patients who are resistant or otherwise unresponsive to treatment with tyrosine kinase inhibitors.
Real-Time Classification Finds High-Risk ALL With Favorable Outcomes
December 8th 2015Real-time classification can identify a previously unrecognized subset of high-risk patients with childhood B-cell acute lymphoblastic leukemia who have excellent chances for cure without further intensification of treatment.