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.
調査の概要
詳細な説明
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.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Thomas AJ Bond, MBChB, BMedSci
- 電話番号:+44 1223 331504
- メール:thomas.bond4@nhs.net
研究場所
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Cambridgeshire
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Cambridge、Cambridgeshire、イギリス、CB2 0BB
- 募集
- Addenbrookes Hospital
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コンタクト:
- Thomas AJ Bond, MBChB, BMedSci
- 電話番号:+44 1223 331504
- メール:thomas.bond4@nhs.net
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コンタクト:
- Jason M Tarkin, PhD, MBBS, FRCP
- メール:jt545@cam.ac.uk
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-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:診断
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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. |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
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Comparison of coronary artery 68Ga-DOTATATE maximum tissue-to-blood ratio (TBRmax) after 16 weeks of anifrolumab compared to baseline
時間枠: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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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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Comparison of ascending aortic 68Ga-DOTATATE TBRmax after 16 weeks of anifrolumab compared to baseline
時間枠:Between baseline and 16 weeks of anifrolumab therapy
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Between baseline and 16 weeks of anifrolumab therapy
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その他の成果指標
結果測定 |
時間枠 |
|---|---|
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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
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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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協力者と研究者
スポンサー
捜査官
- 主任研究者:Jason M Tarkin, PhD MBBS FRCP、University of Cambridge
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- A097234
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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