What Comes Next in Psoriasis Treatment: A Look at the Current Pipeline
IPC Jr. Councilor Towhida Noor reviews the psoriasis pipeline: selective TYK2 inhibitors, long-acting IL-17 and IL-23 biologics, and IL-36 blockade in GPP.
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IPC Jr. Councilor Towhida Noor reviews the psoriasis pipeline: selective TYK2 inhibitors, long-acting IL-17 and IL-23 biologics, and IL-36 blockade in GPP.
IPC Board Member and Treasurer Joel Gelfand, MD, MSCE, is the editor of a new textbook, Psoriasis: An Expert Global Perspective, now available for preorder from Elsevier. He worked with associate editors IPC President Bruce Strober, MD, PhD; IPC Vice President/President-Elect Claudia de la Cruz, MD; and IPC Chief Medical Officer Peter van de Kerkhof, MD, PhD. Nearly 50 authors from 20 countries contributed 30 chapters covering psoriasis from its earliest descriptions through genetics, immunology, and current therapies, with clinical images of psoriasis across diverse skin tones. All royalties support IPC.
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In this video, IPC Councilor Rodrigo Garcia Salinas, MD, a rheumatologist from Argentina, explains how to recognize psoriatic arthritis early, including why joint pain, how long a patient has had psoriasis, and family history can matter more than skin severity alone. He also reviews how imaging helps catch early disease and how to choose treatment based on each patient’s joint, spine, and skin involvement.
IPC President Bruce Strober reviews the link between psoriasis and metabolic disease, drawing on findings from IPC’s recent paper in the Journal of the American Academy of Dermatology (JAAD). He translates this growing body of evidence into five concrete priorities from the 2025 IPC Think Tank for improving cardiometabolic screening and care.
EULAR Points to Consider for the Definition of Clinical and Imaging Features Suspicious for Progression from Psoriasis to Psoriatic Arthritis: Paving the Way for Interception in Psoriatic Arthritis
José-Manuel Carrascosa Carrillo, MD, PhD
University Hospital Germans Trias í Pujol; Autonomous University of Barcelona
Badalona, Spain
IPC Councilor
PUBLICATIONS
EULAR Points to Consider for the Definition of Clinical and Imaging Features Suspicious for Progression from Psoriasis to Psoriatic Arthritis. Zabotti A, De Marco G, Gossec L, et al. Ann Rheum Dis. 2023;82(9):1162-1170. doi:10.1136/ard-2023-224148
Why This Article Was Chosen
It is well-established that psoriatic arthritis (PsA) will affect up to one-third of patients with psoriasis (PsO) at some point during their lives. The development of arthritis significantly impacts the course of the disease and can lead to irreversible sequelae from a relatively early stage. Furthermore, it plays a relevant percentage of the weight in the so-called cumulative life course impairment (CLCI), defined as the extent to which PsO conditions the life of the patient and leads to different —and usually worse—pathways. In contrast to rheumatoid arthritis, where prognostic serological biomarkers are well established and permit prognostic assessment, there is an unmet need to further explore and characterize the transition of PsA to PsO.
Although this is an assumed unmet need in psoriasis, its impact on patient management has been historically moderate in the absence of clear instruments to modify the course of the disease in those patients. This situation may be altered if the results of recent studies are confirmed, which seems to indicate that the early treatment of PsO with biological therapies, even in the absence of signs or symptoms of PsA, could reduce the risk of developing PsA (defined by synovitis) in the future. This paradigm, one of the most discussed currently, represents a significant advancement beyond the current molecular understanding of T-resident memory cells in the potential cure of PsO.
Early detection and the initial indication of the capacity to alter the trajectory of PsO will be, thus, the focus of considerable clinical research and pharmacological industry efforts, which may transform how PsO is managed in the coming years.
The manuscript authored by Zabotti et al. represents the stance of the EULAR (European League Against Rheumatism) task force on the diagnosis and prediction of the progression of PsO to PsA with the available tools and evidence.
Commentary
The manuscript represents the positioning of the EULAR to define the clinical and imaging features that indicate the progression from PsO to PsA. Furthermore, the aim is to standardize the criteria used in clinical trials and practice. In accordance with the usual rigor of the EULAR, with the support of systematic literature reviews, the multidisciplinary team identified and proposed a nomenclature for three distinct stages leading to PsA:
The authors established five overarching principles, some of which are already internalized and known without the need for expert committees, including that people with PsO may develop PsA at different time points or the importance of close collaboration between dermatologists and rheumatologists to understand and optimize PsA prevention, interception, and early diagnosis. Some others are reasonable in clinical practice, such as considering the risk factors for PsA in a patient or the suspicion of early forms of PsA can condition their therapeutic course. The most controversial and important—and may give rise to the greatest conflicts of interest—is that certain systemic treatments of PsO may reduce the risk of transition to PsA.
In a more practical approach, the authors advocated that, in the absence of characteristic serological markers of PsA—which is a clear objective drawback but an opportunity for the meticulous work of the clinician—joint symptoms, particularly arthralgia, should be interpreted as a risk factor in patients with PsO. Imaging tests may be more sensitive than the clinical examination for the detection of musculoskeletal inflammation, considering that up to 40% of people with PsO, even if not affected by joint pain, show subclinical synovio-entheseal alterations detected by ultrasonography and structural entheseal lesions detected by high-resolution peripheral quantitative computed tomography (CT) scan. Considering that joint symptoms are very frequent in the general population, and to avoid overdiagnosis, it is proposed that signs and symptoms continue to be the guide, with imaging as support.
The positioning of the EULAR can be considered as one of extraordinary strategic acumen. The authors do not debate whether there is sufficient data to prove the efficiency of early interception but rather define which patients could be suitable for inclusion in clinical trials and prospective studies to demonstrate this concept. This positioning will be useful in standardizing research and clinical practice in the coming years and will reinforce the work, prestige, and significance of the EULAR itself. In this sense, they lay the foundations for further knowledge. The authors also recall that prevention involves not only the choice of treatment or its early initiation but also the lines that will be most influenced by research. It also involves the commitment of the patient to control risk factors (e.g., weight management) and acquire training on the signs and symptoms of the PsA, which are sometimes more difficult to implement than therapeutic choices.
The article illustrates the positive interdisciplinary collaboration between dermatologists and rheumatologists, which extends beyond the boundaries of international organizations and has been in place for several years through joint clinical initiatives. Meanwhile, the figure (see below) that illustrates the classification and evolution of patients from their predisposition to PsA to its full development is one of the most iconic in recent years in this field and has been continuously reproduced. It may be posited that this is a reference point for a paradigm shift in which we can trust the signals before the evidence occurs. Thus, interception of PsA can be a palpable reality, and the EULAR establishes the rules of the game to measure it.
Image reproduced from Zabotti A et al. Ann Rheum Dis 2023;82:1162–1170. doi:10.1136/ard-2023-224148
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