Effect of Anifrolumab on Arterial Inflammation in Systemic Lupus Erythematosus Study (AISLE)
Effect of Anifrolumab on Arterial Inflammation in Systemic Lupus Erythematosus (AISLE) Study
People with systemic lupus erythematous (SLE) have an increased risk of premature atherosclerotic cardiovascular disease, which is believed to be caused by arterial inflammation. The aim of this study is to investigate the effects an interferon-targeting drug (anifrolumab) used for the treatment of active SLE on arterial inflammation. Arterial inflammation will be measured at baseline and after 4 months of treatment using Positron Emission Tomography (PET)/ Magnetic Resonance Imaging (MRI) with a radio-labelled tracer (68Ga-DOTATATE). Inflammation assessed by PET/MRI will also be compared with clinical disease activity, inflammatory blood markers and in patients with and without coronary artery disease on computed tomography coronary angiography (CTCA) and/or myocardial involvement on MRI.
研究概览
详细说明
It is known that people with SLE are at increased risk of cardiovascular disease because of ongoing inflammation in the body, but the effects of SLE therapies that target inflammation on blood vessels are unknown. Women aged between 35 to 44 are 50 times more likely to have a heart attack than their peers. The risk of stroke, peripheral vascular disease and heart failure is also increased by 2 to 3 fold.
The AISLE study aims to investigate the effects of treating active SLE with an interferon receptor inhibitor (anifrolumab) on arterial inflammation using 68Ga-DOTATATE PET/MRI. Our previous research has shown this imaging method to be effective for tracking macrophage-related arterial inflammation in the cardiovascular system. Patients with active SLE and a clinical SLE Disease Activity Index (SLEDAI) score of ≥4 who meet the eligibility criteria will be invited to participate in the study. All participants will receive anifrolumab therapy in addition to their current SLE treatments, for a total duration of 16 weeks, with imaging performed at baseline and at the end of treatment. CTCA will also be performed, as well as blood sampling for markers of inflammation.
This study will provide valuable information about the effects of anifrolumab on blood vessel inflammation in patients with SLE measured by PET imaging. We expect that this research will also contribute to the wider understanding of how inflammation lowering drugs could be used in general cardiovascular patients to prevent future heart attacks and strokes.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Thomas AJ Bond, MBChB, BMedSci
- 电话号码:+44 1223 331504
- 邮箱:thomas.bond4@nhs.net
学习地点
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Cambridgeshire
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Cambridge、Cambridgeshire、英国、CB2 0BB
- 招聘中
- Addenbrookes Hospital
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接触:
- Thomas AJ Bond, MBChB, BMedSci
- 电话号码:+44 1223 331504
- 邮箱:thomas.bond4@nhs.net
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接触:
- Jason M Tarkin, PhD, MBBS, FRCP
- 邮箱:jt545@cam.ac.uk
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Male or female participants 18 to 70 years of age
- Able to give written, informed consent and to lie flat for scanning
- Fulfil American College of Rheumatology/European Alliance of Associations for Rheumatology 2019 classification criteria for SLE
- Current antinuclear antibody positive (ANA-ELISA ≥1.0, ANA Hep2 positivity)
- Have ≥4 points on the clinical SLEDAI-2K disease activity score
- Stable standard of care SLE therapies for ≥4 weeks
- Prednisolone dosage ≤7.5 mg (or equivalent) daily
- Up to date on required vaccinations (e.g., pneumonia, varicella zoster, and influenza [inactivated/recombinant]) prior to study entry
Exclusion Criteria:
- Women of child-bearing potential not using adequate contraception
- Breastfeeding
- Already taking anifrolumab
- Allergy and/or contraindication to anifrolumab or excipients
- Anaphylaxis to any human gamma globulin therapy
- History of recurrent infections requiring hospitalisation and intravenous (IV) antibiotics (e.g., 3 or more of the same type of infection over the previous 52 weeks)
- Active Hepatitis B virus (HBV) or Hepatitis C virus (HCV) infection, confirmed by (a) HBsAg; or (b) HBcAb and HBV DNA detected above the lower limit of quantitation by reflex testing; or (c) HCV RNA
- Any severe case of herpes zoster (HZ) infection, including, but not limited to: (a) systemic HZ such as herpes encephalitis or ophthalmic herpes involving the retina at any time prior to signing the ICF; (b) recurrent cutaneous HZ defined as 2 or more episodes within 2 years prior to signing the ICF; (c) any HZ infection that has not completely resolved within 12 weeks prior to signing the ICF
- Any active cytomegalovirus or Epstein-Barr virus infection that has not completely resolved within 12 weeks prior to signing the ICF.
- Opportunistic infection requiring hospitalization or IV antimicrobial treatment within 3 years prior to signing the ICF
- Any of the following infections: (a) clinically significant chronic infection (i.e., osteomyelitis, bronchiectasis, etc) within 8 weeks prior to signing the ICF (chronic nail infections are allowed); (b) any infection requiring hospitalization or treatment with IV anti-infectives not completed at least 4 weeks prior to signing the ICF; (c) any infection requiring oral anti-infectives (including antivirals) within 2 weeks prior to signing the ICF
- Any live or attenuated vaccine within 8 weeks prior to signing the informed consent form (ICF). Administration of killed or subunit vaccines is acceptable
- Immunocompromised (known history of a primary immunodeficiency, splenectomy, or any underlying condition that predisposes the participant to infection, or a positive result for human immunodeficiency virus)
- History of active tuberculosis or latent tuberculosis in whom an adequate course of treatment could not be confirmed
- History of cancer (other than squamous or basal cell carcinoma of the skin/cervical cancer in situ treated with curative therapy more than 3 months prior to signing the ICF)
- Receiving other biological therapies or monoclonal antibodies
- Received rituximab or obinutuzumab within the past 24 weeks
- Received belimumab within the past 12 weeks
18. Received cyclophosphamide in the past 6 months 19. Cardiovascular event ≤3 months 20. Contra-indication to MRI or CT scanning 21. Contrast allergy or contrast-nephropathy 22. Active nephritis (>1g protein/24hr or albumin to creatine ratio >100) 23. Active central nervous system lupus 24. Active myocarditis 25. Chronic kidney disease (eGFR <30 mL/min/1.73 m2) 26. Any condition that, in the opinion of the Investigator, would with impact patient safety, ability to complete imaging, or interfere with the interpretation of the study findings
学习计划
研究是如何设计的?
设计细节
- 主要用途:诊断
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Anifrolumab arm
In this single arm of the study patients with patients will undergoing PET/MRI before and after anifrolumab therapy |
Patients with active SLE will undergo 68Ga-DOTATATE PET/MRI before and after four months of anifrolumab therapy. Patients will be treated with anifrolumab for four months to examine the effects of targeting type 1 interferon on inflammation in the cardiovascular system assessed by 68Ga-DOTATATE PET/MRI. |
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Comparison of coronary artery 68Ga-DOTATATE maximum tissue-to-blood ratio (TBRmax) after 16 weeks of anifrolumab compared to baseline
大体时间:Between baseline and following 16 weeks of anifrolumab therapy
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Between baseline and following 16 weeks of anifrolumab therapy
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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Comparison of ascending aortic 68Ga-DOTATATE TBRmax after 16 weeks of anifrolumab compared to baseline
大体时间:Between baseline and 16 weeks of anifrolumab therapy
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Between baseline and 16 weeks of anifrolumab therapy
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其他结果措施
结果测量 |
大体时间 |
|---|---|
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Comparison of abdominal aortic and/or renal artery and/or other arterial 68Ga-DOTATATE TBRmax after 16 weeks of anifrolumab compared to baseline
大体时间:Between baseline and following 16 weeks of anifrolumab therapy
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Between baseline and following 16 weeks of anifrolumab therapy
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Correlation of arterial 68Ga-DOTATATE TBRmax with clinical disease activity graded by the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) and/or British Isles Lupus Assessment Group (BILAG)
大体时间:Between baseline and following 16 weeks of anifrolumab therapy
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Between baseline and following 16 weeks of anifrolumab therapy
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Correlation of arterial 68Ga-DOTATATE TBRmax with blood markers of systemic inflammation
大体时间:Between baseline and following 16 weeks of anifrolumab treatment
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Between baseline and following 16 weeks of anifrolumab treatment
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Comparison of inflammation assessed by 68Ga-DOTATATE PET/MRI (aortic, bone marrow and mediastinal lymph node signals) in patients with coronary artery disease and/or myocardial involvement in SLE versus those without
大体时间:At baseline - single time point
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At baseline - single time point
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Comparison of serum lipids at baseline and follow-up
大体时间:At baseline and following 16 weeks of anifrolumab therapy
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At baseline and following 16 weeks of anifrolumab therapy
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合作者和调查者
调查人员
- 首席研究员:Jason M Tarkin, PhD MBBS FRCP、University of Cambridge
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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