The edition · Dermatology
An oral IL-23 blocker holds clearance to a year
Icotrokinra kept about three-quarters of patients clear or almost clear through week 52, with no new safety signal. Plus a switching study that settles a biosimilar question, why extra histopathology on squamous cell carcinoma adds little, and a mortality figure for transplant recipients that should change your surveillance interval.
The edition in brief
Today's dermatology edition opens with 52-week results from ICONIC-ADVANCE 1 and 2, two phase 3 trials of icotrokinra — an oral peptide that blocks the interleukin-23 receptor — in 1,505 adults with moderate-to-severe plaque psoriasis. Clearance rose to week 24 and held: about 70-75% had IGA 0/1 and PASI 90 during weeks 24 to 52, and about 50% reached IGA 0 and PASI 100. Of those clear or almost clear at week 16, 85-90% still were at week 52. Adverse events matched placebo to week 16 and were fewer than deucravacitinib to week 24, with no new signals to a year. A randomised, double-blind switching study of ABP 654, a ustekinumab biosimilar, took 453 patients through three alternating exposures. Geometric mean ratios for AUCtau and Cmax between weeks 52 and 64 were 0.93 (90% CI 0.89-0.98) and 0.95 (0.90-1.00), inside the 0.8-1.25 margin, with similar efficacy, antidrug antibodies and adverse events. Two nested case-control studies within 19,120 Dutch patients tested whether refined histopathological variables add prognostic value in cutaneous squamous cell carcinoma. In the population-based set, none was significantly associated with metastasis; only solar elastosis showed an inverse association in the risk-matched set. And in 21,503 Australian and New Zealand kidney transplant recipients followed over 212,317 person-years, skin cancer mortality was 11.1 times the general population — 34.5 times for keratinocyte cancer.
Icotrokinra's clearance holds through a year, taken as a tablet
Note icotrokinra as an oral IL-23 receptor blocker with durable year-one clearance, but confirm availability before offering it.
Switching back and forth between a ustekinumab biosimilar and the originator changed nothing measurable
Repeated switching between ABP 654 and reference ustekinumab is supported by pharmacokinetic and immunogenicity data; treat it as interchangeable in a responder.
More detail on the squamous cell carcinoma report does not predict metastasis better
Stratify cutaneous squamous cell carcinoma on conventional variables; extended histopathological reporting did not improve on them.
Ask every transplant patient when their last full skin check was
Give every transplant recipient a named surveillance interval rather than advice to attend regularly.
Skin cancer mortality in kidney transplant recipients is eleven times the population rate
Reset transplant skin surveillance around keratinocyte cancer, which carries a 34.5-fold excess mortality against melanoma's 4.5-fold.
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