The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
Real-world practice indirect comparison between guselkumab, risankizumab, and tildrakizumab: results from an Italian 28-week retrospective study
Abstract
BACKGROUND: Guselkumab, tildrakizumab, and risankizumab, acting on interleukin(IL)23 axis, have been recently approved for psoriasis management. However, real-life data regarding their comparison are scant. OBJECTIVES: The aim of our real life study was to perform an indirect efficacy and safety comparison among anti-IL23s, particularly focusing on difficult-to-treat areas. METHODS: A 2-year single-center retrospective observational study was performed enrolling moderate-to-severe psoriasis patients treated with anti-IL23. For each patient, clinical and demographical data were collected at baseline and at week4, week16, and week28. PASI, BSA, NAPSI, and specific BSA regarding difficult to treat areas were evaluated. RESULTS: One hundred and fifty patients were included in the study: 63 (42%) received guselkumab, 21 (14%) tildrakizumab, and 66 (44%) risankizumab. The three groups were comparable for age, sex, and disease severity, only differing for psoriasis duration, psoriatic arthritis prevalence (higher in guselkumab), and previous systemic treatment failure (lower for tildrakizumab). Mean PASI and BSA significantly reduced from baseline up to week 28 without significant differences among the 3 drugs (reduction of 95-97.3% for PASI and 94.8-96.7% for BSA). No significant differences were registered for PASI75, 90, or 100 responses, in particular, PASI100 was reached by 73.4-85% of patients. As regards difficult-to-treat areas, all the drugs displayed a high efficacy, with significant differences registered only for the rapidity of action on palmoplantar psoriasis. CONCLUSIONS: Our 28-weeks study demonstrated a comparable efficacy and safety profile for all anti-IL23, with guselkumab and risankizumab appearing slightly faster than tildrakizumab particularly on palmoplantar lesions in the short-term.What is already known about this topic?The interleukins (IL) 23/17 axis seems to play a key role in psoriasis management.Guselkumab, tildrakizumab, and risankizumab, selectively blocking the IL23 signaling, have been recently approved for psoriasis management.Real-world data regarding different anti-IL23 comparisons are scant.What does this study add?Our 28-weeks study showed that there were not any significant differences in terms of efficacy and safety between each anti-IL-23 apart from palmoplantar area where guselkumab and risankizumab showed higher efficacy.Globally risankizumab and guselkumab appeared slightly faster than tildrakizumab.Guselkumab, tildrakizumab, and risankizumab are valid weapons for psoriasis management, also for difficult-to-treat areas (scalp, nails, genitalia, lower limbs, and palmo-plantar area).
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In the citing paper
“The identification of the IL-23/Th17 axis as a central driver of psoriasis has led to the development of biologic therapies that selectively interrupt cytokine networks.”
From The Cutaneous Immune Microenvironment in Selected Inflammatory Skin Diseases: Linking Histopathology, Mechanisms, and Targeted Therapy (2026) · cites this paper as [31]
In the citing paper
“Furthermore, increasing evidence supports IL-23 as an upstream regulator of pathogenic T-cell populations; thus, selective IL-23 inhibitors have also shown high efficacy with durable responses, likely by disrupting the maintenance of disease-driving Th17 cells [29,30,31,32].”
From The Cutaneous Immune Microenvironment in Selected Inflammatory Skin Diseases: Linking Histopathology, Mechanisms, and Targeted Therapy (2026) · cites this paper as [31]
In the citing paper
“Therapies targeting IL-17 (monoclonal antibodies against IL-17A or its receptor) have shown rapid and efficient clinical responses by directly suppressing keratinocyte activation and neutrophil recruitment, which are key downstream effects of Th17 immunity.”
From The Cutaneous Immune Microenvironment in Selected Inflammatory Skin Diseases: Linking Histopathology, Mechanisms, and Targeted Therapy (2026) · cites this paper as [31]
In the citing paper
“selective IL-23 inhibitors have also shown high efficacy with durable responses, likely by disrupting the maintenance of disease-driving Th17 cells [29,30,31,32].”
From The Cutaneous Immune Microenvironment in Selected Inflammatory Skin Diseases: Linking Histopathology, Mechanisms, and Targeted Therapy (2026) · cites this paper as [31]
Citations
Cites
Griffiths, C. E. M., Armstrong, A. W., Gudjonsson, J. E., & Barker, J. N. W. N. (2021) · The Lancet · doi:10.1016/s0140-6736(20)32549-6 · Cited by 2,586
Blauvelt, A., Papp, K. A., Griffiths, C. E. M., Randazzo, B. P., Wasfi, Y. S., Shen, Y., Li, S., & Kimball, A. B. (2017) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2016.11.041 · Cited by 899
Reich, K., Armstrong, A. W., Foley, P. A., Song, M., Wasfi, Y. S., Randazzo, B. P., Li, S., Shen, Y., & Gordon, K. B. (2017) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2016.11.042 · Cited by 772
Reich, K., Papp, K. A., Blauvelt, A., Tyring, S. K., Sinclair, R. D., Thaçi, D., Nograles, K. E., Mehta, A., Cichanowitz, N., Li, Q., et al. (2017) · The Lancet · doi:10.1016/s0140-6736(17)31279-5 · Cited by 588
Risankizumab versus Ustekinumab for Moderate-to-Severe Plaque Psoriasis
Papp, K. A., Blauvelt, A., Bukhalo, M., Gooderham, M., Krueger, J. G., Lacour, J. ‐., Menter, A., Philipp, S., Sofen, H. L., Tyring, S. K., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1607017 · Cited by 532
Taylor, P. R., Roy, S., Leal, S. M., Sun, Y., Howell, S. J., Cobb, B. A., Li, X., & Pearlman, E. M. (2013) · Nature Immunology · doi:10.1038/ni.2797 · Cited by 422
Reich, K., Armstrong, A. W., Langley, R. G. B., Flavin, S. K., Randazzo, B. P., Li, S., Hsu, M.-C., Branigan, P. J., & Blauvelt, A. (2019) · The Lancet · doi:10.1016/s0140-6736(19)31773-8 · Cited by 383
Langley, R. G. B., Tsai, T., Flavin, S. K., Song, M., Randazzo, B. P., Wasfi, Y. S., Jiang, J., Li, S., & Puig, L. (2017) · British Journal of Dermatology · doi:10.1111/bjd.15750 · Cited by 341
Reich, K., Gooderham, M., Thaçi, D., Crowley, J., Ryan, C., Krueger, J. G., Tsai, T., Flack, M., Gu, Y., Williams, D., et al. (2019) · The Lancet · doi:10.1016/s0140-6736(19)30952-3 · Cited by 301
Warren, R. B., Blauvelt, A., Poulin, Y. P., Beeck, S., Kelly, M., Wu, T., Geng, Z., & Paul, C. F. (2020) · British Journal of Dermatology · doi:10.1111/bjd.19341 · Cited by 210
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Research works printed but not linked: 3
- Megna M, Fabbrocini G, Ruggiero A, et al. Efficacy and safety of risankizumab in psoriasis patients who failed anti-IL-17, anti-12/23and/or anti IL-23: preliminary data of a real-life 16-week retrospective study. Dermatol Ther. 2020;5:e14144.
- Tildrakizumab for psoriasis. Aust Prescr. 2019;42(1):40–41.
- Ruggiero A, Fabbrocini G, Cinelli E, et al. Efficacy and safety of guselkumab in psoriasis patients who failed ustekinumab and/or anti-interleukin-17 treatment: a real-life 52-week retrospective study. Dermatol Ther. 2021;34(1):e14673.
Cited by
Sorted by citations
The Role of Teledermatology During the COVID-19 Pandemic: A Narrative Review
Ruggiero, A., Martora, F., Fabbrocini, G., Villani, A., Marasca, C., Megna, M., Fornaro, L., Comune, R., & Potestio, L. (2022) · Clinical, Cosmetic and Investigational Dermatology · doi:10.2147/ccid.s377029 · Cited by 46
Self-citationTinca, A. C., Cozac-Szoke, A. R., & Cotoi, O. S. (2026) · Dermatopathology · doi:10.3390/dermatopathology13020022 · Cited by 1
Metadata
- Authors
- Megna, M., Tommasino, N., Potestio, L., Battista, T., Ruggiero, A., Noto, M., Fabbrocini, G., & Genco, L.
- Affiliations
- University of Naples Federico II (IT)
- Corresponding author
- Megna, Matteo
- ORCID
- Venue
- Journal of Dermatological Treatment
- Publisher
- Informa UK Limited
- Published
- 2022-05-29
- Volume
- 33
- Issue
- 6
- Pages
- 2813-2820
- ISSN
- 0954-6634 (ISSN-L)
- 1471-1753
- OpenAlex
- W4281288090
- Cited by
- 90
- References
- 29
- Citations by year
- 2026: 13 · 2025: 10 · 2024: 16 · 2023: 37 · 2022: 13
- FWCI
- 7.28
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Dermatological Treatment (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Health Sciences › Medicine › Dermatology › Dermatology and Skin Diseases
- Health Sciences › Medicine › Rheumatology › Spondyloarthritis Studies and Treatments
- Keywords
- psoriasis, guselkumab, risankizumab, tildrakizumab, indirect comparison, real-world effectiveness, PASI response, palmoplantar psoriasis, psoriatic arthritis, drug safety, biologic therapy, Italian patients
- MeSH terms
- Antibodies, Monoclonal, Humans, Interleukins, Psoriasis, Retrospective Studies, Severity of Illness Index, Treatment Outcome, Interleukin-23, Antibodies, Monoclonal, Humanized
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