Skip to main content
OpenTrials
Completed

NCT Number: NCT04308616

Utility of Squamous Cell Carcinoma Antigen (SCCA) in Psoriasis

Squamous Cell Carcinoma Antigen (SCCA) contributes to the pathogenesis of psoriasis by inhibiting cell apoptosis, exacerbating epidermal hyperplasia and skin inflammation. Three studies have shown a correlation between blood levels of SCCA and the severity of psoriasis.

Clinical scores of psoriasis severity are used in consultation to guide treatment of the disease (initiation of systemic therapy, dose escalation) but they suffer from several pitfalls: lack of inter- and intra-observer reproducibility, consumption of medical time.

A readily available, inexpensive (24 euros) blood marker could be an interesting alternative to these clinical scores.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Dermatology Service, University Hospital, Tours

Tours, 37044, France

About this study

Squamous Cell Carcinoma Antigen (SCCA) contributes to the pathogenesis of psoriasis by inhibiting cell apoptosis, exacerbating epidermal hyperplasia and skin inflammation. Three studies have shown a correlation between blood levels of SCCA and the severity of psoriasis.

Clinical scores of psoriasis severity are used in consultation to guide treatment of the disease (initiation of systemic therapy, dose escalation). The PASI (Psoriasis Assessment Severity Index, minimum score 0, maximum 72) is the most widely used. It suffers from several pitfalls: lack of inter- and intra-observer reproducibility, consumption of medical time. This PASI score was "unavoidable" in the international clinical studies used to obtain marketing authorisation for medicines. The PGA (Physician global assessment) is simpler and less time-consuming, ranging from 0 to 4, but is not very discriminating. More recently, a "Simplified Psoriasis Index" (proSPI) health professional score has been developed, which correlates well with PASI for the severity component of psoriasis and with quality of life for the psychological component of the disease. It is less time-consuming to establish than PASI, but suffers like all clinical scores from a problem of inter- and intra-observer reproducibility.

A readily available, inexpensive (24 euros) blood marker could be an interesting alternative to these clinical scores.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years old
  • Patient with skin psoriasis (new and untreated or being treated, flare-up or stable, possibly bleached)
  • Requiring a blood sample for disease or treatment monitoring

Exclusion criteria

  • History of invasive mucosal squamous cell carcinoma, or squamous cell carcinoma of the skin with lymph node or visceral recurrence.
  • Patient under guardianship or curatorship
  • Opposition to participation in the study

Treatment and study plan

Blood Samples

Other

Blood samples

Primary outcomes

  1. SCCA blood concentration

    Time frame: Baseline, 3 months and 6 months

    SCCA blood concentration will be measured at each visit

Secondary outcomes

  1. Assess correlations between SCCA blood concentration and proSPI severity score

    Time frame: Baseline, 3 months and 6 months

    proSPI severity score (0-50) will be evaluated at each visit

  2. Assess correlations between SCCA blood concentration and proSPI psychosocial score

    Time frame: Baseline, 3 months and 6 months

    proSPI psychosocial score (0-10) will be evaluated at each visit

  3. Assess correlations between SCCA blood concentration and proSPI treatment score

    Time frame: Baseline, 3 months and 6 months

    proSPI treatment score (0-10) will be evaluated at each visit

  4. Assess correlations between SCCA blood concentration and C reactive protein (CRP)

    Time frame: Baseline, 3 months and 6 months

    CRP will be measured at each visit

  5. Assess correlations between SCCA blood concentration and neutrophil/lymphocyte ratio

    Time frame: Baseline, 3 months and 6 months

    neutrophil/lymphocyte ratio will be measured at each visit

Sponsors and collaborators

Lead sponsor

University Hospital, Tours

Other

Registry information

Acronym: SCCAPSO

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Mar 16, 2020
Registry last updated
Jun 1, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.