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Review
. 2024 Jan;25(1):15-33.
doi: 10.1007/s40257-023-00818-z. Epub 2023 Sep 17.

Chronic Prurigo Including Prurigo Nodularis: New Insights and Treatments

Affiliations
Review

Chronic Prurigo Including Prurigo Nodularis: New Insights and Treatments

Svenja Müller et al. Am J Clin Dermatol. 2024 Jan.

Abstract

Chronic prurigo (CPG) is a neuroinflammatory, fibrotic dermatosis that is defined by the presence of chronic pruritus (itch lasting longer than 6 weeks), scratch-associated pruriginous skin lesions and history of repeated scratching. Patients with CPG experience a significant psychological burden and a notable impairment in their quality of life. Chronic prurigo of nodular type (CNPG; synonym: prurigo nodularis) represents the most common subtype of CPG. As CNPG is representative for all CPG subtypes, we refer in this review to both CNPG and CPG. We provide an overview of the clinical characteristics and assessment of CPG, the burden of disease and the underlying pathophysiology including associated therapeutic targets. The information provided results from a PubMed search for the latest publications and a database search for current clinical trials (ClinicalTrials.gov, EU Clinical Trials Register [European Medicines Agency]; using the following terms or combinations of terms: 'chronic prurigo', 'prurigo', 'prurigo nodularis', 'pathophysiology', 'therapy', 'biologics', 'treatment'). Dupilumab is the first authorized systemic therapy by the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) for CNPG to date. Topical and systemic agents that are currently under investigation in clinical randomized, placebo-controlled phase II and III trials such as biologics (e.g., nemolizumab, vixarelimab/KPL-716, barzolvolimab/CDX-0159), small molecules (ruxolitinib cream, povorcitinib/INCB054707, abrocitinib) and the opioid modulator nalbuphine are highlighted. In the last past 15 years, several milestones have been reached regarding the disease understanding of CPG such as first transcriptomic analysis, first terminology, first guideline, and first therapy approval in 2022, which contributed to improved medical care of affected patients. The broad range of identified targets, current case observations and initiated trials offers the possibility of more drug approvals in the near future.

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Conflict of interest statement

Svenja Müller is or was advisor, speaker or investigator for Galderma, Incyte Inc., Eli Lilly, Sanofi/Regeneron and LEO Pharma outside the submitted work. Claudia Zeidler is or was advisor, speaker or investigator for Novartis, Janssen, Pfizer, UCB, Lilly, AbbVie, Boehringer Ingelheim, Sanofi, Regeneron, Leo, Galderma, Dermasence, Beiersdorf, Unna Akademie. She was a consultant for Sanofi and Allmiral. All outside the submitted work. Sonja Ständer is an investigator for Celldex, Clexio, Dermasence, Galderma, GSK, Incyte, Kiniksa, Novartis, Sanofi, Trevi. She is a consultant and/or member of advisory boards for AbbVie, Almirall, Beiersdorf, Benevolent, Bionorica, Cara, Celgene, Clexio, DS Biopharma, Eli Lilly, Escient, Galderma, Kiniksa, Klinge Pharma, Leo Pharma, Maruho, Menlo, P.G. Unna Academy, Pfizer, Sanofi, Symbio Research, Trevi, Vanda, Vifor, WebMD.

Figures

Fig. 1
Fig. 1
Therapeutic targets for chronic nodular prurigo (CNPG). In CNPG therapy, different targets can be addressed to improve pruriginous lesions and chronic pruritus. The adaptive immune response and the peripheral nerve system provide many promising therapeutic targets for biologics, Janus kinase inhibitors and opioid modulators. IL interleukin, KOR κ-opioid receptor, MOR μ-opioid receptor
Fig. 2
Fig. 2
Clinical presentation of a chronic nodular prurigo (CNPG) patient treated with dupilumab. An 84-year-old patient with CNPG, initially (a) and 4 months after initiation of therapy with dupilumab 300 mg subcutaneously every 2 weeks (b)

References

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