Whats New PsA? (4.3.2026)
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This episode of the RheumNow Podcast, hosted by Dr. Jack Cushwood on April 3, 2026, covers key updates from the American Academy of Dermatology (AAD) annual meeting, focusing on psoriatic arthritis (PsA) and psoriasis. Major highlights include the publication of the Affinity trial, which found combination therapy with goselcomab and galumab significantly improved ACR50, ACR20, and ACR70 responses in PsA patients—though it didn’t meet its primary MDA endpoint—suggesting potential for future combination biologic use. The AXIS study revealed that 27% of PsA patients have axial involvement via imaging, a higher rate than previously thought, which may influence treatment paradigms. The TOGETHER PSA trial demonstrated that adding terzepatide to ixakizumab led to dramatically higher ACR50 and weight loss rates in overweight/obese PsA patients, underscoring the value of combination metabolic and immunologic therapy. Additionally, breplositinib, a novel TIC2-JAK1 inhibitor, showed strong efficacy in refractory skin and muscle disease, though a 10% rate of serious infectious events at the 30mg dose raises safety concerns. The FDA issued a safety warning about Avacapan due to 76 cases of drug-induced liver injury, including 7 cases of rare vanishing bile duct syndrome (VBDS) with fatal outcomes, reinforcing the need for vigilance in monitoring. The episode also discusses broader healthcare trends, including the psychiatrist shortage and the growing role of advanced practice providers in managing chronic inflammatory diseases like rheumatology. Key takeaways include: 1) Combination therapies (biologic + metabolic agents) are emerging as powerful tools in PsA, especially in overweight patients; 2) Axial disease is more prevalent in PsA than previously recognized, warranting better imaging and treatment strategies; 3) New TIC2 inhibitors like envuducitinib and breplositinib show promise but require careful risk-benefit assessment due to infection and liver toxicity; 4) Aggressive, treat-to-target management improves pregnancy outcomes in autoimmune diseases; 5) The growing reliance on APPs in rheumatology demands structured training and collaboration. The overall tone is cautiously optimistic, emphasizing innovation while underscoring safety and patient-centered care.
Combination therapy with ixakizumab and terzepatide significantly improves ACR50 and weight loss in overweight/obese PsA patients.
Axial involvement in PsA is more common (27%) than previously thought, suggesting a need for routine imaging and tailored treatment.
New TIC2 inhibitors like breplositinib show strong efficacy but carry a higher risk of serious infections at higher doses.
Aggressive treat-to-target management improves pregnancy outcomes in autoimmune diseases like RA and lupus.
Advanced practice providers are increasingly essential in rheumatology care, requiring formal onboarding and collaboration.
Pregnancy and Autoimmune Disease Updates
Highlights from the LUNA registry and other studies on pregnancy outcomes in lupus, myositis, and rheumatoid arthritis, emphasizing the importance of treat-to-target management and the lack of association between SSA antibodies and fetal loss.
Affinity Trial: Combination Biologic Therapy in PsA
“ACR50 was 32 versus 5%. P.003. ACR20, 66 versus 44%. ACR70, 27 versus 16%. So this is highly significant.”
AXIS Study: Prevalence of Axial Disease in PsA
“This is a different animal, right? And we certainly know that there's some subset. We've always said it was, I think we always said it was around 20% of PSA patients would have axial disease. This one, by imaging, said it was 27%.”
TOGETHER PSA Trial: Ixakizumab + Terzepatide in PsA
“The primary endpoint, ACR50 plus weight loss was achieved in 32% in the combination arm and only 0.8% in the Ixakizumab group alone.”
New Therapies and FDA Safety Warnings
“There was more serious infectious events on the Brepo 30 milligram dose group at 10% SIE rate. That's high versus the 1% SIE rate with placebo.”
“The primary endpoint, ACR50 plus weight loss was achieved in 32% in the combination arm and only 0.8% in the Ixakizumab group alone.”
“ACR50 was 32 versus 5%. P.003. ACR20, 66 versus 44%. ACR70, 27 versus 16%. So this is highly significant.”
“There was more serious infectious events on the Brepo 30 milligram dose group at 10% SIE rate. That's high versus the 1% SIE rate with placebo.”
Host
Dr. Jack Cushwood
person
Ixakizumab
product
Terzepatide
product
Avacapan
product
SSA Antibody
other
TOGETHER PSA Trial
other
Goselcomab
product
Affinity Trial
other
Breplositinib
product
FDA
organization
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