TY - JOUR
T1 - Standards of Genetic Testing in the Diagnosis and Prognostication of Systemic Mastocytosis in 2022
T2 - Recommendations of the EU-US Cooperative Group
AU - Hoermann, Gregor
AU - Sotlar, Karl
AU - Jawhar, Mohamad
AU - Kristensen, Thomas
AU - Bachelot, Guillaume
AU - Nedoszytko, Boguslaw
AU - Carter, Melody C.
AU - Horny, Hans Peter
AU - Bonadonna, Patrizia
AU - Sperr, Wolfgang R.
AU - Hartmann, Karin
AU - Brockow, Knut
AU - Lyons, Jonathan J.
AU - Kluin-Nelemans, Hanneke C.
AU - Hermine, Olivier
AU - Akin, Cem
AU - Broesby-Olsen, Sigurd
AU - Triggiani, Massimo
AU - Butterfield, Joseph H.
AU - Schwaab, Juliana
AU - Reiter, Andreas
AU - Gotlib, Jason
AU - Metcalfe, Dean D.
AU - George, Tracy I.
AU - Orfao, Alberto
AU - Valent, Peter
AU - Arock, Michel
N1 - Funding Information:
D.D.M., J.J.L., and M.C.C. were supported by the Division of Intramural Research , National Institute of Allergy and Infectious Diseases, National Institutes of Health . P.V. was supported by the Austrian Science Fund ( FWF ) (grant nos. F4704-B20 and P32470-B ).
Publisher Copyright:
© 2022 American Academy of Allergy, Asthma & Immunology
PY - 2022/8
Y1 - 2022/8
N2 - Mastocytosis comprises rare heterogeneous diseases characterized by an increased accumulation of abnormal mast cells in various organs/tissues. The pathogenesis of mastocytosis is strongly linked to the presence of KIT-activating mutations. In systemic mastocytosis (SM), the most frequent mutation encountered is KIT p.D816V, whose presence constitutes one of the minor diagnostic criteria. Different techniques are used to search and quantify the KIT p.D816V mutant; however, allele-specific quantitative PCR and droplet digital PCR are today the most sensitive. The analysis of the KIT p.D816V allele burden has undeniable interest for diagnostic, prognostic, and therapeutic monitoring. The analysis of non–mast cell hematological compartments in SM is similarly important because KIT p.D816V multilineage involvement is associated with a worse prognosis. In addition, in advanced forms of SM, mutations in genes other than KIT are frequently identified and affect negatively disease outcome and response to therapy. Thus, combined quantitative and sensitive analysis of KIT mutations and next-generation sequencing of other recurrently involved myeloid genes make it possible to better characterize the extent of the affected cellular compartments and additional molecular aberrations, providing a more detailed overview of the complex mutational landscape of SM, in relation with the clinical heterogeneity of the disease. In this article, we report the latest recommendations of the EU-US Cooperative Group presented in September 2020 in Vienna during an international working conference, on the techniques we consider standard to detect and quantify the KIT p.D816V mutant in SM and additional myeloid mutations found in SM subtypes.
AB - Mastocytosis comprises rare heterogeneous diseases characterized by an increased accumulation of abnormal mast cells in various organs/tissues. The pathogenesis of mastocytosis is strongly linked to the presence of KIT-activating mutations. In systemic mastocytosis (SM), the most frequent mutation encountered is KIT p.D816V, whose presence constitutes one of the minor diagnostic criteria. Different techniques are used to search and quantify the KIT p.D816V mutant; however, allele-specific quantitative PCR and droplet digital PCR are today the most sensitive. The analysis of the KIT p.D816V allele burden has undeniable interest for diagnostic, prognostic, and therapeutic monitoring. The analysis of non–mast cell hematological compartments in SM is similarly important because KIT p.D816V multilineage involvement is associated with a worse prognosis. In addition, in advanced forms of SM, mutations in genes other than KIT are frequently identified and affect negatively disease outcome and response to therapy. Thus, combined quantitative and sensitive analysis of KIT mutations and next-generation sequencing of other recurrently involved myeloid genes make it possible to better characterize the extent of the affected cellular compartments and additional molecular aberrations, providing a more detailed overview of the complex mutational landscape of SM, in relation with the clinical heterogeneity of the disease. In this article, we report the latest recommendations of the EU-US Cooperative Group presented in September 2020 in Vienna during an international working conference, on the techniques we consider standard to detect and quantify the KIT p.D816V mutant in SM and additional myeloid mutations found in SM subtypes.
KW - allele burden
KW - diagnosis
KW - KIT mutations
KW - Mast cell
KW - mastocytosis
KW - next-generation sequencing
KW - prognosis
U2 - 10.1016/j.jaip.2022.03.001
DO - 10.1016/j.jaip.2022.03.001
M3 - Review article
C2 - 35283331
AN - SCOPUS:85127335143
SN - 2213-2198
VL - 10
SP - 1953
EP - 1963
JO - The Journal of Allergy and Clinical Immunology: In Practice
JF - The Journal of Allergy and Clinical Immunology: In Practice
IS - 8
ER -