Cited by 172Mast cells and histamineFood Allergy and Anaphylaxis ResearchDrug-Induced Adverse Reactions

Omalizumab for the treatment of unprovoked anaphylaxis in patients with systemic mastocytosis

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Carter, Melody C., Robyn, Jamie A., Bressler, Peter B., Walker, John C., Shapiro, Gail G., Metcalfe, Dean D.·2007·Journal of Allergy and Clinical Immunology

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Crossref · 10.1016/j.jaci.2007.03.032

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  • Response to additional drugs, including multitargeted tyrosine kinase inhibitors (in patients with SM, such as midostaurin) and anti-IgE therapy (omalizumab), may be considered an indirect sign of MCA or MCAS.

    “Response to additional drugs, including multitargeted tyrosine kinase inhibitors (in patients with SM, such as midostaurin) and anti-IgE therapy (ie, omalizumab) may be considered an indirect sign of MCA or MCAS.”

    From Selecting the Right Criteria and Proper Classification to Diagnose Mast Cell Activation Syndromes: A Critical Review (2021) · cites this paper as [81]

    The PATIENT 1 and PATIENT 2 sections (page not available) report fewer or no anaphylaxis episodes after omalizumab in two patients with systemic mastocytosis. The paper does not present treatment response as an indirect sign of mast-cell activation or MCAS, and it does not address midostaurin or other multitargeted tyrosine kinase inhibitors. (LLM, conf=0.84)

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  1. Melody C. Carter, MD a Jamie A. Robyn, MD, PhD a Peter B. Bressler, MD b John C. Walker, MD c Gail G. Shapiro, MD d Dean D. Metcalfe, MD a From a the National Institutes of Health, National Institute of Allergy and Infectious Diseases, Laboratory of Allergic Disease, Bethesda, Md; b Caro- lina Allergy and Asthma, Chapel Hill, NC; c the Northwest Allergy and Asthma Center, University of Washington Children's Hospital and Re- gional Medical Center, Richland, Wash; and d the Northwest Allergy and Asthma Center, University of Washington School of Medicine, Seattle, Wash. E-mail: mcarter@niaid.nih.gov. Supported by the Intramural Research Program of the National Institutes of Health, National Institute of Allergy and Infectious Diseases. Disclosure of potential conflict of interest: P. B. Bressler has received grant support from Genentech/Novartis and is on the speakers' bureau for Sanofi-Aventis, AstraZeneca, and Schering-Plough. The rest of the authors have declared that they have no conflict of interest. Editor's note: Readers interested in this topic may also be interested in a forthcoming Letter to the Editor in which Siebenhaar and colleagues pre- sent a case report of ''Successful treatment of cutaneous mastocytosis with anti-IgE.'' Look for this article in the July 2007 issue of the JACI, or ahead of print publication in the Articles in Press section of the JACI Web site, www.jacionline.org.

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Authors
Carter, M. C., Robyn, J. A., Bressler, P. B., Walker, J. C., Shapiro, G. G., & Metcalfe, D. D.
Affiliations
  • National Institutes of Health (US)
  • Allergy, Asthma and Clinical Research Center (US)
  • University of Washington (US)
Corresponding author
Carter, Melody C.
Venue
Journal of Allergy and Clinical Immunology
Publisher
Elsevier BV
Published
2007-06
Volume
119
Issue
6
Pages
1550-1551
ISSN
0091-6749 (ISSN-L)
OpenAlex
W2061452912
Cited by
172
References
4
Citations by year
2026: 4 · 2025: 11 · 2024: 2 · 2023: 5 · 2022: 1 · 2021: 14 · 2020: 8 · 2019: 17 · 2018: 9 · 2017: 12 · 2016: 7 · 2015: 12 · 2014: 13 · 2013: 12 · 2012: 9
FWCI
3.80
Type
journal article
Language
en
Open access
Locations
  • Journal of Allergy and Clinical Immunology (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institutes of Health
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
  • Health Sciences › Medicine › Immunology and Allergy › Food Allergy and Anaphylaxis Research
  • Health Sciences › Medicine › Pharmacology › Drug-Induced Adverse Reactions
Keywords
omalizumab, systemic mastocytosis, urticaria pigmentosa, anti-IgE therapy, mast cell activation, c-kit D816V mutation, hypotension, mast cell proliferation, mast cell survival, mast cell mediators, mast cell degranulation
MeSH terms
Omalizumab, Adolescent, Anaphylaxis, Antibodies, Anti-Idiotypic, Antibodies, Monoclonal, Humans, Male, Middle Aged, Urticaria Pigmentosa, Receptors, IgE, Anti-Allergic Agents, Mastocytosis, Systemic, Antibodies, Monoclonal, Humanized

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