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Withdraw Drug in Stable IgG4-Related Disease

Evaluation and Prediction of Relapse Risk After Glucocorticoid and Immunosuppressant Withdrawal in Patients With Stable IgG4 Related Disease: An Open-labeled Multi-centric Randomized Controlled Study From China

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04124861
Enrollment
138
Registered
2019-10-11
Start date
2020-06-23
Completion date
2023-06-30
Last updated
2022-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autoimmune Diseases

Keywords

Immunoglobulin G4-Related Disease

Brief summary

Evaluation and prediction of relapse risk after glucocorticoid or immunosuppressant withdrawal in patients with stable IgG4 related disease: a prospective cohort study from china.

Detailed description

IgG4-related disease (IgG4-RD) is a chronic autoimmune disease with a relapsing-remitting course. For patients in remission, glucocorticoid (GC) and immunosuppressant are used to be maintained for a long time in fear of disease flare. Long-term GC and immunosuppressant could bring a lot of side-effects and economic burden. Whether and when patients with stable disease should withdraw GC or immunosuppressant? How about the relapse risk respectively? What are the risk factors for disease flare? All the above remain unclear. The aim of this study is to explore the relapse risk after GC or immunosuppressant withdrawal in IgG4-RD patients with stable disease and to establish a predictive model for risk stratification. Meanwhile the investigators aim to testify the effects of immunosuppressant in preventing IgG4-RD relapse. This study is a prospective cohort clinical trial.

Interventions

DRUGDrug free, IS monotherapy and GC combined with IS

Follow-up intervals: Every 3 months (3th, 6th, 9th, 12th, 15th, 18th month).

Sponsors

Chinese PLA General Hospital
CollaboratorOTHER
Peking University People's Hospital
CollaboratorOTHER
The People's Hospital of Hebei Province
CollaboratorOTHER
Shengjing Hospital
CollaboratorOTHER
Tongji Hospital
CollaboratorOTHER
Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. All patients must meet the following diagnostic criteria of IgG4RD (2011): 1)Swelling, sclerosing and inflammatory involvement of one or more organ, including sclerosing pancreatitis, sialadenitis (Mikulicz disease), sclerosing cholangitis, inflammatory pseudotumors, retroperitoneal or mediastinal fibrosis, interstitial nephritis, hypophysitis, sclerosing dacryoadenitis, inflammatory aortic aneurysm, lymphadenopathy, or other inflammatory conditions; 2)Elevated serum IgG4 (\>1.35 g/L); 3)Histopathologic features of fibrosis and/or lymphocytic and polyclonal plasma cell infiltration (and IgG4+ plasma cells on immunohistology when performed). Patients fulfill 1)+2)+3) are diagnosed as definite IgD4RD, 1)+2): possible IgG4RD; 1)+3): probable IgG4RD. exclusion of other diseases. 2. Disease stabilized more than one year (Responder Index \< 2 points) 3. Dose of Glucocorticoid(GC): prednisone (or equivalent) ≤ 7.5mg/d for more than 6 months 4. Immunosuppressant: one of the following drugs, the same dose maintain at least 3 months (Mycophenolate mate \<= 1g/d or Leflunomide \<=20mg/d or Methotrexate \<=12.5mg/w or Azathioprine \<=100mg/d).

Exclusion criteria

1. Patient was diagnosed other connective tissue diseases 2. Patient with tumor 3. Women during pregnancy or planning pregnancy 4. Patient with active infections, including HIV, HCV, HBV, TB, etc. 5. Patient with severe irreversible organ damage 6. Active IgG4-RD, responder index \>= 2 points 7. Stable condition less than one year. 8. Patient with two or more immunosuppressive agents. 9. Biological agents (such as CD20 monoclonal antibody and TNF-a inhibitor) have been used for half a year before admission. 10. Patient with IgG4-RD recurrence during hormone reduction in the past.

Design outcomes

Primary

MeasureTime frameDescription
The difference of recurrent rate of IgG4-RD among three groups.One and half yearClinical recurrence definition: any item of IgG4-RD Responder Index \>=2,new organ involvement; with or without elevated serum IgG4 levels. Serum recurrence definition: Serum IgG4 level was higher than baseline level, IgG4-RD Responder Index was higher than or equal to 1 point, without clinical symptom or imaging deterioration.

Secondary

MeasureTime frameDescription
The changes of serum IgG4 levelsOne and half yearLevel of serum IgG4(mg/dL)
The changes of serum IgG levelOne and half yearLevel of serum IgG(g/L)
The changes of IgG4-RD Responder IndexOne and half yearAccording to IgG4-RD responder Index Validation Study (Version: 13, December, 2015)
The changes of ESROne and half yearSerum erythrocyte sedimentation rate(mm/h)
The percentages of adverse eventsOne and half yearAdverse effect of drugs
The changes of serum hsCRP levelOne and half yearLevel of serum high-sensitivity C-reactive protein level(mg/L)

Countries

China

Contacts

Primary Contactlinyi peng, MD.
drpenglinyi@163.com+8615810395901

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026