HLADQA1*05 Genotype and the Efficacy of Treatment With Infliximab in Chinese Population Crohn's Disease
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Azathioprine, Infliximab.
- Who it may be relevant to
- Registry conditions: Crohn Disease, Infliximab. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Preemptive HLADQA1*05 Genotyping for the Use of Infliximab in Chinese Crohn's Disease：A Multicenter, Prospective, Controlled, Randomized Study
Overview
Crohn's disease (CD) is a chronic non-specific inflammatory disease of the intestine. Infliximab (IFX) is a kind of one of the anti-tumor necrosis factor agents (anti-TNF) and is the main clinical treatment drug for Crohn's disease, but approximately 30-50% of patients develop a secondary non-response to respond within one year. The main cause of secondary non-response failure is the formation of anti-IFX anti-drug antibodies (ADA). The human leukocyte antigen (HLA) gene is a complex allele that has been associated with susceptibility to a variety of diseases. Studies have shown that HLADQA1\*05 allele carriage significantly increases the immunogenicity of anti-tumor necrosis factor agents (anti-TNF) and the risk of ADA formation, resulting in a significant reduction in the efficacy of IFX. Our previous retrospective study found an increased risk of ADA, IFX failure to respond and discontinuation in patients with HLADQA1\*05 variants, and that IFX in combination with immunosuppression improved clinical outcomes in wild-type genotype patients, whereas combination therapy in patients with variant genotype did not optimize clinical outcomes significantly. Therefore, we believe that the impact of HLADQA1\*05 on the efficacy of IFX in the Chinese population is unclear, and the combination of immunosuppressants in patients with variant HLADQA1\*05 genotype remains to be validated due to insufficient sample size. We hypothesized that HLADQA1\*05 wild-type CD patients would have better clinical remission when treated with IFX than HLADQA1\*05 variant patients and that the combination of immunosuppressants would improve the outcome in wild-type patients but not in variant patients. By advancing this project, we hope to provide high quality evidence on the clinical use of IFX in Crohn's disease in the Chinese population and help physicians to be more selective in the use of IFX alone or in combination with azathioprine, or to switch treatment in a timely manner.
Interventions
- Drug Azathioprine
azathioprine in combination with Infliximab, with a dose of 1-2 mg/kg/d. - Drug Infliximab
5mg/kg for the first dose, and the same dose at weeks 2 and 6 after the first dose and every 8 weeks thereafter. Treatment with single Infliximab or combined azathioprine, respectively.
Primary outcome measures
- Clinical remission without corticosteroid use at 102 weeks [Time frame: 102 weeks]
Secondary outcome measures (6)
- Clinical response at 14 weeks [Time frame: 14 weeks]
- Positive for ADA [Time frame: 102 weeks]
- IFX Intensive Therapy [Time frame: 102 weeks]
- IFX Failure to Respond [Time frame: 102 weeks]
- Adverse drug events [Time frame: 102 weeks]
- IFX discontinuation [Time frame: 102 weeks]
Eligibility criteria
Inclusion criteria
- Participants with Crohn's disease who meet the diagnostic criteria of the Consensus Opinion on the Diagnosis and Treatment of Inflammatory Bowel Disease (Beijing, 2018)
- Meet the indications for IFX use
- CDAI score of 220-450; age≥18 years, regardless of gender
- Participants or family members able to understand the study protocol and willing to participate in this study by providing written informed consent
Exclusion criteria
- NUDT 15 CT and TT genotypes; previous treatment with IFX and/or other anti-TNF biologics
- Participants who are proposed to have given birth and/or breastfeeding in the 12 months
- those with immunosuppressive intolerance or contraindications
- concurrent chronic diseases or factors of other systems (including severe cardiopulmonary, hepatic and renal, neurological, psychiatric, rheumatic and immune diseases, alcoholism, drug dependence, other chronic active diseases and long-term hormonal or immunosuppressive drugs)
- Excluding infectious diseases (tuberculosis, etc.)
- Excluding tumor-related diseases (lymphoma, gastrointestinal tract tumors, etc.)
- any medical condition/combined surgery/medication/other clinically significant abnormal laboratory tests which, in the judgment of the investigator, may affect the results of the test
- Known refusal or inability to follow protocol requirements for any reason (including planned clinical visits and examinations)
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT05813860 · 2023ZSLYEC-123