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Real-World Considerations of Candidacy for Biologics in Hidradenitis Suppurativa.
Shih, Terri; De, Devea; Daveluy, Steven D; Hogeling, Marcia; Lowes, Michelle A; Sayed, Christopher; Shi, Vivian Y; Hsiao, Jennifer L.
Affiliation
  • Shih T; David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • De D; Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, USA.
  • Daveluy SD; Department of Dermatology, Wayne State University, Detroit, MI, USA.
  • Hogeling M; Division of Dermatology, University of California Los Angeles, Los Angeles, CA, USA.
  • Lowes MA; The Rockefeller University, New York, NY, USA.
  • Sayed C; Department of Dermatology, UNC School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Shi VY; Department of Dermatology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
  • Hsiao JL; Department of Dermatology, University of Southern California, 1441 Eastlake Ave, Ezralow Tower, Suite 5301, Los Angeles, CA, 90033-9174, USA. j.hsiao.publications@gmail.com.
Am J Clin Dermatol ; 23(6): 749-753, 2022 Nov.
Article in En | MEDLINE | ID: mdl-35930133
Hidradenitis suppurativa (HS) is a chronic, progressive inflammatory skin disease that is often recalcitrant to multiple treatments. In determining biologic candidacy for patients with HS, we propose a paradigm shift away from Hurley staging and towards consideration of other variables. Biologics represent a long-term treatment option for HS that may serve as a disease-modifying agent. These medications are typically initiated in patients with moderate to severe disease, which, based on inclusion criteria in clinical trials, is often defined as Hurley stage II or III disease, at which point irreversible tissue damage has already occurred. In real-world clinical settings, these considerations include treatments tried and failed, predicted disease trajectory, disease characteristics beyond lesion type, impact of disease on patients' functional status and quality of life, and patient comorbidities, venturing away from the limitations of Hurley stage designations. Future clinical trials may benefit from inclusion of recalcitrant Hurley stage I patients, which may then re-shape treatment guidelines and insurance coverage and improve patient access to biologic treatments.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Products / Hidradenitis Suppurativa Type of study: Guideline / Prognostic_studies Aspects: Patient_preference Limits: Humans Language: En Journal: Am J Clin Dermatol Journal subject: DERMATOLOGIA Year: 2022 Document type: Article Affiliation country: United States Country of publication: New Zealand

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Products / Hidradenitis Suppurativa Type of study: Guideline / Prognostic_studies Aspects: Patient_preference Limits: Humans Language: En Journal: Am J Clin Dermatol Journal subject: DERMATOLOGIA Year: 2022 Document type: Article Affiliation country: United States Country of publication: New Zealand