FDA grants Breakthrough Designation to bezuclastinib for nonadvanced SM
Bezuclastinib received Breakthrough Therapy Designation from the FDA for certain patients with nonadvanced 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.
Tryptase genotyping helps determine whether a high tryptase level reflects disease or genetics in systemic mastocytosis (SM).
Patients with systemic mastocytosis (SM) face significantly increased risks of melanoma and other skin cancers.
HT-KIT cut KIT protein levels by more than 80% and halted tumor growth in systemic mastocytosis (SM) models.
A patient with systemic mastocytosis suffered a life-threatening immune reaction after receiving an mRNA-1273 COVID-19 booster.