Proposed European Competence Network on Mastocytosis-American Initiative in Mast Cell Diseases (ECNM-AIM) Response Criteria in Advanced Systemic Mastocytosis.
Advanced systemic mastocytosis
Avapritinib
International Working-Group for Myeloproliferative Neoplasms Research and Treatment and European Competence Network on Mastocytosis
KIT D816V
Midostaurin
Pure pathologic response
Journal
The journal of allergy and clinical immunology. In practice
ISSN: 2213-2201
Titre abrégé: J Allergy Clin Immunol Pract
Pays: United States
ID NLM: 101597220
Informations de publication
Date de publication:
08 2022
08 2022
Historique:
received:
21
02
2022
revised:
23
05
2022
accepted:
25
05
2022
pubmed:
21
6
2022
medline:
17
8
2022
entrez:
20
6
2022
Statut:
ppublish
Résumé
Advanced systemic mastocytosis (AdvSM) is characterized by the presence of KIT D816V and other somatic mutations (eg, in SRSF2, ASXL1, and RUNX1) in 95% and 60% to 70% of patients, respectively. The biological and clinical consequences of AdvSM include multilineage involvement (eg, associated hematologic neoplasm) in 60% to 80% of patients, variable infiltration and damage (C-findings) of predominantly bone marrow and visceral organs through affected mast cell (MC) and non-MC lineages, and elevated levels of serum tryptase. Recently, the treatment landscape has substantially changed with the introduction of the multikinase/KIT inhibitor midostaurin and the selective KIT D816V inhibitor avapritinib. In this review, we discuss the evolution of AdvSM response criteria that have been developed to better capture clinical benefit (eg, improved responses and progression-free and overall survival). We propose refined response criteria from European Competence Network on Mastocytosis and American Initiative in Mast Cell Diseases investigators that use a tiered approach to segregate the effects of histopathologic (eg, bone marrow MC burden, tryptase), molecular (eg, KIT D816V variant allele frequency), clinical (eg, C-findings), and symptom response on long-term outcomes. These response criteria require evaluation in future prospective clinical trials of selective KIT inhibitors and other novel agents.
Identifiants
pubmed: 35724948
pii: S2213-2198(22)00585-2
doi: 10.1016/j.jaip.2022.05.034
pii:
doi:
Substances chimiques
Proto-Oncogene Proteins c-kit
EC 2.7.10.1
Tryptases
EC 3.4.21.59
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Intramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
2025-2038.e1Informations de copyright
Copyright © 2022. Published by Elsevier Inc.