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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.

In this edition
01
Clinical update

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.

2 min · The British journal of dermatologyRead →
Primary outcome
IGA 0/1 and PASI 90 response, with IGA 0 and PASI 100, through week 52
Effect
About 70-75% IGA 0/1 and PASI 90 during weeks 24-52; about 50% IGA 0 and PASI 100; 85-90% of week-16 responders maintained to week 52
02Research

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.

2 min · The British journal of dermatologyRead →
03Research

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.

2 min · The British journal of dermatologyRead →
04Pearl

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.

1 minRead →
05Practice changer

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.

2 min · The British journal of dermatologyRead →

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