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临床试验/NCT07104058
NCT07104058招募中不适用

A Prospective Study on the Effect of Minimal Residual Disease Detected by Fibroblast Activation Protein PET / CT on the Recurrence of IgG4-related Disease

Luo Yaping1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2025年5月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
46
试验地点
1
主要终点
Recurrence rate of IgG4-related disease.

研究概览

简要总结

This study intends to use the new technology of fibroblast activation protein PET / CT to study whether the tiny residual lesions detected by 68Ga-FAPI PET / CT are related to the recurrence of IgG4-RD in patients with IgG4-RD who have been clinically evaluated for complete remission after treatment.

详细描述

This prospective randomized controlled study will enroll IgG4-RD patients who have achieved clinical complete remission with negative 18F-FDG PET/CT findings after glucocorticoid and immunosuppressant therapy. Following enrollment, all participants will undergo 68Ga-FAPI PET/CT screening.Based on the results, patients will be stratified into two groups: Group A (68Ga-FAPI PET/CT negative, indicating MRD-negative status) and Group B (68Ga-FAPI PET/CT positive, indicating MRD-positive status). Group A (MRD-negative) will receive no intervention and enter treatment withdrawal with observational follow-up. Group B (MRD-positive) patients will be randomized 1:1 into either the experimental subgroup B1 (continuing low-dose glucocorticoids with or without immunosuppressant maintenance therapy) or the control subgroup B2 (treatment withdrawal with observational follow-up). All participants will be followed for 18 months with quarterly clinical disease activity assessments to document relapse. Randomization will be performed using an online randomization system, with only the endpoint assessors blinded to group allocation while other investigators and study subjects remain aware of the randomization results.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •age 18-75 years old ;
  • •Meet the 2019 ACR / EURLAR IgG4-RD diagnostic criteria ;
  • •The disease was stable for more than 1 year, and the clinical evaluation of the disease was complete remission * ;
  • •Glucocorticoid dosage ≤ prednisone 7.5mg / d × 6 months or more, or combined with an immunosuppressive therapy ( mycophenolate mofetil ) Ester ≤ 1.0g / d, leflunomide ≤ 20mg / d, methotrexate ≤ 15mg / w, azathioprine ≤ 100mg / d, iguratimod ≤ 25mg Bid )

排除标准

  • •( 1 ) Combined with other connective tissue disease patients ( 2 ) patients with tumor ; ( 3 ) women during pregnancy or planning pregnancy ; ( 4 ) active infection, including HIV, HCV, HBV, TB, etc. ; ( 5 ) Severe irreversible organ damage ; ( 6 ) In the active stage of the disease, the IgG4-RD reaction index score of the single affected organ was 2 points ; ( 7 ) stable condition less than 1 year ; ( 8 ) patients who relapsed within 1 year of previous hormone reduction and withdrawal ; ( 9 ) Combination of two or more immunosuppressive agents.

研究组 & 干预措施

A(68Ga-FAPI PET / CT negative patients)

Other

Group A (MRD-negative) will receive no intervention and enter treatment withdrawal with observational follow-up.

干预措施: 68Ga-FAPI PET / CT (Diagnostic Test)

B(68Ga-FAPI PET / CT positive patients)

Other

Group B (68Ga-FAPI PET/CT positive, indicating MRD-positive status). Group B (MRD-positive) patients will be randomized 1:1 into either the experimental subgroup B1 (continuing low-dose glucocorticoids with or without immunosuppressant maintenance therapy) or the control subgroup B2 (treatment withdrawal with observational follow-up).

干预措施: 68Ga-FAPI PET / CT (Diagnostic Test)

结局指标

主要结局

Recurrence rate of IgG4-related disease.

时间窗: 18 months after enrollment

All participants will be followed for 18 months with quarterly clinical disease activity assessments to document relapse.

次要结局

未报告次要终点

研究者

发起方
Luo Yaping
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Luo Yaping

Medical Doctor (M.D.), Chief Physician, Professor, Assistant Director

Peking Union Medical College Hospital

研究点 (1)

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