Efficacy and safety of mammalian target of rapamycin inhibitors in systemic mastocytosis: A nationwide French pilot study

Systemic mastocytosis (SM) corresponds to a rare and heterogeneous spectrum of diseases characterized by the accumulation of atypical mast cells (MCs). Advanced mastocytosis (Adv‐SM) is associated with poor survival; in contrast, patients with non‐advanced SM (non‐Adv‐SM) usually have a normal life...

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Published inAmerican journal of hematology Vol. 99; no. 6; pp. 1095 - 1102
Main Authors Moraly, Josquin, Rossignol, Julien, Rouzaud, Claire, Gabas, Thomas, Bouktit, Hassiba, Lhermitte, Ludovic, Canioni, Danielle, Fraitag, Sylvie, Bruneau, Julie, Barete, Stéphane, Suarez, Felipe, Ballul, Thomas, Meni, Cécile, Polivka, Laura, Terriou, Louis, Launay, David, Bouillet, Laurence, Gaudy‐Marqueste, Caroline, Gousseff, Marie, Le Mouel, Edwige, Neel, Antoine, Ranta, Dana, Jaussaud, Roland, Guilpain, Philippe, Frenzel, Laurent, Agopian, Julie, Dubreuil, Patrice, Greco, Céline, Dimicoli‐Salazar, Sophie, Heiblig, Mael, Gourguechon, Clément, Tournilhac, Olivier, Javier, Rose‐Marie, Castelain, Florence, Cabrera, Quentin, Gourin, Marie Pierre, Wierzbicka‐Hainaut, Ewa, Torregrosa‐Diaz, Jose Miguel, Bulai, Cristina, Lavigne, Christian, Hoarau, Cyrille, Arock, Michel, Damaj, Gandhi, Lortholary, Olivier, Hermine, Olivier
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.06.2024
Wiley Subscription Services, Inc
Wiley
SeriesAmerican Journal of Hematology
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Online AccessGet full text
ISSN0361-8609
1096-8652
1096-8652
DOI10.1002/ajh.27323

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Summary:Systemic mastocytosis (SM) corresponds to a rare and heterogeneous spectrum of diseases characterized by the accumulation of atypical mast cells (MCs). Advanced mastocytosis (Adv‐SM) is associated with poor survival; in contrast, patients with non‐advanced SM (non‐Adv‐SM) usually have a normal life expectancy but may experience poor quality of life. Despite recent therapeutic progress including tyrosine kinase inhibitors, new treatment options are needed for refractory and/or intolerant patients with both severely symptomatic and Adv‐SM. In vitro, the mTOR pathway is activated in MCs from patients bearing the KIT D816V mutation. Furthermore, rapamycin induces the apoptosis of KIT D816V MCs selectively. In this nationwide study, we report the outcomes of patients diagnosed with SM and treated with a mammalian target of rapamycin inhibitor (imTOR) within the French National Reference Center for mastocytosis (CEREMAST). All patients registered were relapsing, treatment‐refractory, or ineligible for other cytoreductive therapy. Non‐Adv‐SM patients received imTOR as a monotherapy (rapamycin/everolimus), and Adv‐SM patients received imTOR as a monotherapy or in combination with cytarabine. The objective response rate (ORR) in non‐Adv‐SM was 60% (partial response in 40% and major response in 20%), including reductions in skin involvement, mediator release symptoms, and serum tryptase. In the Adv‐SM group, the ORR was 20% (including one major response and one partial response, both in patients with a KIT D816V mutation), which enabled a successful bridge to allogeneic stem cell transplantation in one patient. Our results suggest that imTOR treatment has potential benefits in patients with SM harboring a KIT D816V mutation.
Bibliography:Olivier Lortholary, Olivier Hermine, Josquin Moraly, and Julien Rossignol contributed equally to this study.
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ISSN:0361-8609
1096-8652
1096-8652
DOI:10.1002/ajh.27323