Guselkumab efficacious among patients of psoriasis with skin of color

Written By :  Dr. Kamal Kant Kohli
Published On 2023-10-24 04:45 GMT   |   Update On 2023-10-24 07:18 GMT

USA: Guselkumab exhibited fast and significant clearance in body and scalp psoriasis after one dose in patients with skin of color in a phase 3b trial results released by Jannsen.In the study, TREMFYA demonstrated significant skin clearance, rapid scalp psoriasis clearance and improvement in health-related quality of life outcomes. In this previously understudied population, no new...

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USA: Guselkumab exhibited fast and significant clearance in body and scalp psoriasis after one dose in patients with skin of color in a phase 3b trial results released by Jannsen.

In the study, TREMFYA demonstrated significant skin clearance, rapid scalp psoriasis clearance and improvement in health-related quality of life outcomes. In this previously understudied population, no new safety signals were reported through Week 16. These data will be presented today at the 2023 Fall Clinical Dermatology Conference in Las Vegas, Nevada.

"VISIBLE reinforces that to overcome the barriers of underrepresentation, undertreatment, and lack of access to care that many people of color with plaque psoriasis face, additional data about the disease journey are needed to improve treatment outcomes and quality of life for people with skin of color," said Mona Shahriari, M.D., Central Connecticut Dermatology and VISIBLE Steering Committee member. “In addition to insightful data, VISIBLE has provided the medical community with key learnings around study design and representative clinical imagery that have the potential to tangibly address the unmet needs of the diverse psoriasis patient population."

Guselkumab Skin Clearance Data at Week 16 Poster:

  • At Week 16, 74% of patients receiving TREMFYA achieved an Investigator’s Global Assessment (IGA) score of cleared (0) or minimal disease (1) and 57.1% achieved at least a 90% improvement in the Psoriasis Area Severity Index (PASI 90) response (near complete skin clearance), successfully meeting the study’s co-primary endpoints versus placebo (0% and 3.8%, respectively).
  • After only three doses, significantly greater improvements in disease signs and symptoms (e.g., change from baseline in PASI scores) were observed in patients receiving TREMFYA (84.5%) versus placebo (8.3%). Significantly greater improvements in body surface area (BSA) involvement were observed in patients receiving TREMFYA (77.9%) versus placebo (0.9%).
  • Approximately one-third of patients receiving TREMFYA achieved complete skin clearance PASI 100 (29.9%), IGA 0 (32.5%) versus none for placebo (0%) at week 16.

Guselkumab Rapid and Significant Scalp Psoriasis Clearance Data at Week 16 Poster:

  • As early as Week 4, after only one dose of TREMFYA, the mean percentage improvement from baseline Psoriasis Scalp Severity Index (PSSI) was 53.8% in patients treated with TREMFYA versus 12.3% for placebo.
  • After one dose of TREMFYA, 26.3% of participants achieved complete scalp clearance (ss-IGA 0) versus none for placebo (0%) at Week 4.
  • At Week 16, 71.9% of patients receiving TREMFYA achieved complete scalp clearance versus 10% for placebo.

Guselkumab Health-Related Quality of Life (HRQoL) and Post-Inflammatory Pigmentation Data Poster:

  • At baseline, VISIBLE participants reported disease signs and symptoms have significant impact on HRQoL. They also reported moderate effect of skin discoloration on HRQOL. Post-inflammatory pigmentation is part of the natural history of psoriasis and is known to be a key factor impacting quality of life.
  • VISIBLE was prospectively designed to also collect clinical photographs, colorimetry measures, clinician reported outcomes and patient reported outcomes.
  • At Week 16, improvements in the Psoriasis Symptoms and Signs Diary (PSSD), Dermatology Life Quality Index (DLQI) and Skin Discoloration Impact Evaluation Questionnaire (SDIEQ) were significantly greater in patients receiving TREMFYA versus placebo across all skin tones.

VISIBLE will continue to expand understanding of plaque PsO by aiming to generate an expansive, longitudinal library of thousands of clinical images capturing the disease’s presentation across all skin tones. Only 4-19% of images in dermatology textbooks showcase conditions in darker skin tones, illustrating the opportunity for VISIBLE to contribute to medical education by helping clinicians recognize clinical presentation across all skin tones and supporting patients to better understand their diagnosis with images of other patients who look like them.

The study used a holistic, community-driven approach that leads with intentional site and investigator selection from diverse communities, involvement of a racially and ethnically diverse steering committee of dermatologists involved in protocol development and study execution, community engagement and awareness building, as well as educational and cultural training support for clinical investigators. Colorimetry was utilized as an objective method to determine baseline skin tone and track progress of psoriatic lesions to help minimize potential investigator subjectivity and bias.

“The VISIBLE study is a direct representation of where scientific innovation meets inclusivity as it will continue to generate new data and imagery to help create a world where people of color living with plaque psoriasis, and their providers, can have more informed discussions about treatment options,” said Jennifer Davidson, D.O., Vice President, Medical Affairs, Immunology, Janssen Scientific Affairs, LLC. “Partnering alongside community-driven clinicians and researchers is critical to create new research standards where diversity is both expected and necessary to represent the communities we all serve. Our aim is for VISIBLE to help transform research processes and education for so many more patients.”

TREMFYA is the first IL-23 inhibitor approved in the U.S. to treat both adults with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy and adults with active psoriatic arthritis (PsA).

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