New gene findings will help guide treatment in infant leukemia
Researchers identified partner genes that fuse with MLL, driving fatal leukemia in infants. Accurate predictions and treatments are expected based on this knowledge.
Researchers identified partner genes that fuse with MLL, driving fatal leukemia in infants. Accurate predictions and treatments are expected based on this knowledge.
A new study demonstrates advances in optimizing treatments and quality of life for patients with multiple myeloma. The research explores optimal induction therapies, advance care planning, and a potential new first-line therapy for non-Hodgkin lymphoma.
A new three-drug combination has shown a highly effective regimen in treating newly diagnosed patients with multiple myeloma, with partial responses or better seen in all 66 patients. The treatment also resulted in encouraging complete or near-complete responses at 54 percent.
Dr. Donald F. Steiner has made significant contributions to the understanding of insulin secretion and related disorders through his research on proinsulin and C-peptide measurement. His work has led to major improvements in therapeutic insulin development, diagnosis of pancreatic tumors, and islet transplants.
A JAK2 inhibitor has been shown to provide significant and durable relief for patients with myelofibrosis, a rare and debilitating bone marrow disorder. The drug has demonstrated a 33% reduction in spleen volume and improvements in quality of life, exercise capacity, and fatigue.
Researchers found that vitamin D levels in patients with diffuse large B-cell lymphoma were strongly associated with cancer progression and overall survival. Patients with deficient vitamin D levels had a 1.5-fold greater risk of disease progression.
Researchers have developed a new protocol to improve the survival of patients with acute promyelocytic leukemia and chronic myeloid leukemia, particularly in developing countries. The study found a significant improvement in early mortality and long-term outcomes, with high rates of complete remission.
Researchers found that omacetaxine achieved durable responses in CML patients with the T315I mutation, who have limited treatment options. The injectable drug works by a different mechanism than current therapies and has shown promise for expanded use.
Researchers developed a new approach to prevent graft-versus-host disease and enhance immune recovery after haploidentical transplants. The study showed long-term protection from graft-versus-host disease in 25 of 26 patients, with improved immune system reconstitution.