M
Matthew J. Koster
Researcher at Mayo Clinic
Publications - 129
Citations - 1325
Matthew J. Koster is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Medicine & Giant cell arteritis. The author has an hindex of 14, co-authored 79 publications receiving 688 citations. Previous affiliations of Matthew J. Koster include Leiden University Medical Center.
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Journal ArticleDOI
Large-vessel giant cell arteritis: diagnosis, monitoring and management
TL;DR: Recent data suggest that biologic therapies, such as tocilizumab, may be effective and safe steroid-sparing options for patients with GCA, however, data specifically evaluating the management of LV-GCA are limited.
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Predictors of relapse and treatment outcomes in biopsy-proven giant cell arteritis: a retrospective cohort study
Cristian Labarca,Matthew J. Koster,Cynthia S. Crowson,Ashima Makol,Steven R. Ytterberg,Eric L. Matteson,Kenneth J. Warrington +6 more
TL;DR: Females and patients with hypertension or diabetes at GCA diagnosis have more relapses during follow-up and patients treated with an initial oral prednisone dose >40 mg/day achieved earlier prednis one discontinuation.
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The Mayo Clinic Histiocytosis Working Group Consensus Statement for the Diagnosis and Evaluation of Adult Patients With Histiocytic Neoplasms: Erdheim-Chester Disease, Langerhans Cell Histiocytosis, and Rosai-Dorfman Disease
Gaurav Goyal,Jason R. Young,Matthew J. Koster,W. Oliver Tobin,Robert Vassallo,Jay H. Ryu,Caroline J. Davidge-Pitts,Maria D. Hurtado,Aishwarya Ravindran,Julio C. Sartori Valinotti,N. Nora Bennani,Mithun Vinod Shah,Karen L. Rech,Ronald S. Go +13 more
TL;DR: This consensus statement represents a joint document from a multidisciplinary group of physicians at Mayo Clinic who specialize in the management of adult histiocytic neoplasms and consists of evidence- and consensus-based recommendations on when to suspect these neoplasm and what tests to order for the diagnosis and initial evaluation.
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Recent advances in the clinical management of giant cell arteritis and Takayasu arteritis
TL;DR: Abatacept and ustekinumab are promising targets for therapy in LVV but further investigation is needed before routine use is considered, and utility in newly diagnosed immunosuppressive-naïve patients is less well established.
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Ruxolitinib is more effective than other JAK Inhibitors to treat VEXAS Syndrome: a retrospective multi center study.
Maël Heiblig,Marcela A. Ferrada,Matthew J. Koster,Thomas Barba,Mathieu Gerfaud-Valentin,Arsène Mekinian,Henrique Coelho,Gaelle Fossard,Fiorenza Barraco,Lionel Galicier,Boris Bienvenu,Pierre Hirsch,Guillaume Vial,Anne-Blandine Boutin,J. Galland,Guillaume Le Guenno,Adrien Bigot,Warrington J Kenneth,Tanaz A. Kermani,Peter C. Grayson,Bhavisha A Patel,David B. Beck,Yvan Jamilloux,Pierre Fenaux,Pierre Sujobert +24 more
TL;DR: Heiblig et al. as discussed by the authors performed a retrospective analysis of 30 patients with VEXAS syndrome treated with different Janus kinase (JAK) inhibitors, finding encouraging evidence supporting the use of the JAK1/2 inhibitor ruxolitinib with clinical remissions and reductions in steroid use seen in the majority of patients.