Review explores impact of targeted KIT drugs on SM anaphylaxis
KIT-targeting drugs can lower abnormal mast cell burden and reduce the frequency and severity of life-threatening reactions.
KIT-targeting drugs can lower abnormal mast cell burden and reduce the frequency and severity of life-threatening reactions.
Only 25% of patients with indolent SM report their disease is well controlled, despite most clinicians believing control is common.
If approved, dibutepinephrine could offer patients with SM a needle-free epinephrine option that is easier to carry and use.
Gastrointestinal mastocytosis occurs in about one-third of patients with systemic mastocytosis and strongly predicts bone marrow involvement.
Research on shortened telomeres in children’s mast cells may help develop ways to trigger natural disease remission in SM.
Bezuclastinib received Breakthrough Therapy Designation from the FDA for certain patients with nonadvanced SM.
Scientists found five genetic changes in people with systemic mastocytosis (SM), including two never reported before.
Osteoporosis affects 42% of people with indolent systemic mastocytosis (ISM) and is linked to spine and peripheral fractures.
The commonly known KIT D816V mutation appeared only in systemic disease, while other KIT mutations were seen in skin-limited cases.
In patients with SM and blood cancer, a stem cell transplant rapidly removed the disease-causing mutation, but tryptase levels took longer.