Study shows most children with mastocytosis improve over time
Most children with mastocytosis limited to the skin improve or fully resolve, often within a few years, rather than progress to SM.
Most children with mastocytosis limited to the skin improve or fully resolve, often within a few years, rather than progress to SM.
The application is supported by results from the SUMMIT trial. A decision is expected by December 30, 2026.
Aggressive SM should be considered in older adults with unexplained symptoms when no primary cancer is identified.
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.