Study reveals gap in how indolent systemic mastocytosis control is viewed
Only 25% of patients with indolent SM report their disease is well controlled, despite most clinicians believing control is common.
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.
Patients with systemic mastocytosis can safely extend venom immunotherapy (VIT) maintenance intervals to 12 weeks after five years.