PMID- 30697883 OWN - NLM STAT- MEDLINE DCOM- 20200114 LR - 20200114 IS - 1529-8019 (Electronic) IS - 1396-0296 (Linking) VI - 32 IP - 3 DP - 2019 May TI - The efficacy of omalizumab in Cutaneous Mastocytosis: A case series. PG - e12848 LID - 10.1111/dth.12848 [doi] AB - BACKGROUND: Mastocytosis describes a heterogeneous group of disorders arising from a clonal proliferation of mast cells. Given the lack of curative treatments for the cutaneous form, there is a significant need for superior therapies. Omalizumab is a recombinant DNA-derived humanized IgG monoclonal antibody that selectively binds to human immunoglobulin E (IgE). It represents a potential treatment for the management of cutaneous mastocytosis, which currently has no standard treatment. METHODS: Two patients were treated with subcutaneous omalizumab 300 mg every 4 weeks. DISCUSSION: Patient 1 experienced 50% reduction in cutaneous infiltration and moderate improvement in pruritus. Patient 2 underwent 90% complete clearance of cutaneous lesions and reported full resolution of pruritus. The median duration of treatment was 24 weeks and time to response was 8 weeks. No significant changes in tryptase levels were observed. Both patients experienced injection site reactions. CONCLUSION: We provide evidence from two cases supporting the efficacy of IgE-mediated therapy in the treatment of cutaneous mastocytosis. Even at a higher-than-standard dose (300 mg vs. 150 mg), the drug was well-tolerated. As we await the results of pivotal clinical trials, omalizumab appears to be a promising treatment option in patients with cutaneous mastocytosis unresponsive to traditional therapies. CI - (c) 2019 Wiley Periodicals, Inc. FAU - Hinojosa, Tiffany AU - Hinojosa T AUID- ORCID: 0000-0001-5809-698X AD - Dermatology Department, Center for Clinical Studies, Houston, Texas. FAU - Lewis, Daniel J AU - Lewis DJ AD - Department of Internal Medicine, Memorial Sloan Kettering Cancer Center, New York, New York. AD - Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, Texas. FAU - Vangipuram, Ramya AU - Vangipuram R AD - Department of Dermatology, University of Texas Health Science Center at Houston, Houston, Texas. FAU - Safeer, Laraib AU - Safeer L AD - School of Medicine, Baylor College of Medicine, Houston, Texas. FAU - Mui, Uyen Ngoc AU - Mui UN AD - Dermatology Department, Center for Clinical Studies, Houston, Texas. FAU - Haley, Christopher AU - Haley C AD - Dermatology Department, Center for Clinical Studies, Houston, Texas. FAU - Konoplev, Sergej AU - Konoplev S AD - Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas. FAU - Tyring, Stephen K AU - Tyring SK AD - Dermatology Department, Center for Clinical Studies, Houston, Texas. AD - Department of Dermatology, University of Texas Health Science Center at Houston, Houston, Texas. LA - eng PT - Case Reports PT - Journal Article DEP - 20190220 PL - United States TA - Dermatol Ther JT - Dermatologic therapy JID - 9700070 RN - 0 (Anti-Allergic Agents) RN - 2P471X1Z11 (Omalizumab) RN - 37341-29-0 (Immunoglobulin E) SB - IM MH - Adult MH - Anti-Allergic Agents/*administration & dosage/adverse effects/pharmacology MH - Female MH - Humans MH - Immunoglobulin E/immunology MH - Injections, Subcutaneous MH - Mastocytosis, Cutaneous/*drug therapy/immunology MH - Middle Aged MH - Omalizumab/*administration & dosage/adverse effects/pharmacology MH - Pruritus/drug therapy/etiology MH - Treatment Outcome OTO - NOTNLM OT - IgE OT - maculopapular cutaneous mastocytosis OT - mastocytosis OT - omalizumab EDAT- 2019/01/31 06:00 MHDA- 2020/01/15 06:00 CRDT- 2019/01/31 06:00 PHST- 2018/07/24 00:00 [received] PHST- 2018/10/12 00:00 [revised] PHST- 2019/01/26 00:00 [accepted] PHST- 2019/01/31 06:00 [pubmed] PHST- 2020/01/15 06:00 [medline] PHST- 2019/01/31 06:00 [entrez] AID - 10.1111/dth.12848 [doi] PST - ppublish SO - Dermatol Ther. 2019 May;32(3):e12848. doi: 10.1111/dth.12848. Epub 2019 Feb 20.