Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT05473403

Validation of a Prognostic Score for Steroid Therapy Response in Acute Severe Autoimmune Hepatitis

Autoimmune hepatitis (AIH) is a chronic liver disease, which is characterized by the increase of immunoglobulin G (IgG) level, the presence of auto-antibodies and a typical histology, in the absence of other liver disease.

Due to the heterogeneity of AIH manifestations, different scoring systems have been validated in order to make a reliable diagnosis. The two most recent scoring systems are: the revised International Autoimmune Hepatitis Group (IAIHG) criteria and the IAIHG simplified criteria. The second one is recommended by the European Association for the Study of the Liver (EASL) clinical practice guidelines (CPGs).

The EASL clinical practice guidelines suggests that the treatment of ASAIH (Acute Severe AIH) is high doses of corticosteroids (superior to 1mg/kg/day) as early as possible and a lack of improvement within seven days should lead to listing for emergency liver transplantation (LT). However, the "lack of improvement" is not objectively defined and the grading of recommendation is III (Opinions of respected authorities).

The hypothesis of the study is that the previously developed decisional score on a retrospective series will prospectively allow the differentiation between patients with ASAIH (Acute Severe AIH) who respond to corticosteroid therapy and should be maintained on treatment and patients who do not respond and should be rapidly evaluated for LT. The score will be computed at day 3 since corticosteroid introduction.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Angers, Service Hepato-gastro-enterologie, Angers, France

Loading trial locations.

About this study

All the interventions (blood samples, imagery examinations, visits, liver biopsy, corticosteroid therapy, liver transplantation) will be performed following the standard of care for ASAIH. The investigators of the participating centers will not change their standard management for the study protocol. The management will follow the recommendation of EASL CPGs.

The prognostic score will allow to distinguish between patient's responders and non-responders to corticosteroid therapy in ASAIH. This knowledge will avoid the prolonged duration of the corticosteroid therapy in patients for whom this therapy is futile or harmful and rapidly select the patients for LT. Of course considering that the created score is decisional whether a patient is a candidate for LT, a prospective validation is mandatory to use it as a clinical tool for the day-to-day practice. This is the first prospective study on ASAIH.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • Strong clinical suspicion of severe acute autoimmune hepatitis defined by the presence of increased IgG and/or autoantibodies and/or histology characteristic of the disease in the absence of other causes of severe acute hepatitis.
  • International Normalized Ratio (INR) ≥ 1.5
  • Informed, written consent
  • Patient having the rights to French social insurance

Exclusion criteria

  • Previous medical history of chronic liver disease including autoimmune liver disease (AIH, Primary Biliary Cholangitis (PBC), Primary Sclerosing Cholangitis (PSC) , alcoholic hepatitis etc.)
  • Other causes of acute severe hepatitis:
  • Hepatitis A Virus (HAV) hepatitis, defined by HAV Immunoglobulin M (IgM) antibodies
  • Hepatitis B Virus (HBV) hepatitis, defined by HBs antigen and HBV IgM antibodies
  • Hepatitis E Virus (HEV) hepatitis, defined by HEV IgM antibodies or positive HEV-RNA in immunosuppressed patients
  • Drug induced hepatitis, histologically proved or induced by well-known hepatotoxic substances
  • Acute hypoxemic hepatitis, context of shock, hypoxemia or heat shock
  • Budd-Chiari syndrome, diagnosed by imagery (Doppler ultrasound, CT scan)
  • Acute hepatitis in the context of a HELLP (Hemolysis, Elevated Liver enzymes and a Low Platelet count) syndrome or acute fatty liver of pregnancy
  • Use of corticosteroids 1 month before inclusion
  • Pregnant or lactating woman
  • Curator or guardianship or patient placed under judicial protection
  • Participation in other interventional research during the study

Treatment and study plan

Corticosteroid therapy

Other

Administration of high doses of corticosteroids as early as possible. Patient non-responder to treatment should lead to listing for emergency liver transplantation (LT).

Primary outcomes

  1. Prospectively validate the previously elaborated SURFASA-score, evaluating its ability to predict non-response outcome to corticosteroid therapy in a new population of patients with acute severe autoimmune hepatitis.

    Time frame: Day 90

    Patient response within 90 days to corticosteroid therapy defined as: responders (alive without LT) or non-responders (dead or transplanted) within 90 days since corticosteroid therapy introduction.

Secondary outcomes

  1. The association between infection occurrence and death during hospitalization

    Time frame: participation period (treatment+follow-up): 12 months

    Documented infections during hospitalization

  2. the management of infected ASAIH patients in usual practice

    Time frame: participation period (treatment+follow-up): 12 months

    Antibiotic therapy : doses

  3. The risk factors for early AIH flair after corticosteroid therapy response.

    Time frame: D90

    The frequency of AIH flair

  4. The risk factors for AIH recurrence after liver transplantation

    Time frame: participation period (treatment+follow-up): 12 months

    AIH recurrence

  5. The evolution of patients after LT

    Time frame: participation period (treatment+follow-up): 12 months

    Retransplantation, alive, death

  6. The evolution of patients not treated with corticosteroids but meeting the inclusion and non-inclusion criteria

    Time frame: participation period (treatment+follow-up): 12 months

    Retransplantation, alive, death

  7. The prognostic factors for survival in patients treated with corticosteroids who underwent or not LT

    Time frame: participation period (treatment+follow-up): 12 months

    quality of the graft, immunosuppression, rejection episode,

  8. The association of histological features (liver biopsy) with response to corticosteroids and survival at 90 days since admission

    Time frame: 90 days

    Presence of centrilobular necrosis and inflammatory infiltration

Study contacts

Contact information is provided by the study sponsor or research team.

Eleonora DE MARTIN, MD, PhD

CONTACT

[email protected]

33 (0)1.45.59.64.33

Jean-Charles DUCLOS-VALLEE, MD, PhD

CONTACT

[email protected]

33 (0)1.45.59.64.28

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Validation of a Prognostic Score for Steroid Therapy Response in Acute Severe Autoimmune Hepatitis, a National Prospective Multicentre Study

Acronym: PRO-SURFASA

Important dates

Study start
2024
Primary completion
2027
Study completion
2028
First posted
Jul 25, 2022
Registry last updated
Mar 13, 2024

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.