Interleukin-1 Blockade for Treatment of Cardiac Sarcoidosis

Overview

Sarcoidosis is a heterogeneous disorder of unknown etiology whose signature lesions are granulomatous inflammatory infiltrates in involved tissues. Tissue commonly affected are lungs, skin, eyes, lymph nodes and the heart. In this latter case, cardiac sarcoidosis (CS) can lead to atrioventricular (AV) blocks, ventricular arrhythmias, heart failure (HF) and sudden cardiac death. Similar to other involved organs, cardiac disease generally progresses from areas of focal inflammation to scar. However, the natural history of CS is not well characterized complicating an immediate and definitive diagnosis. The management of CS often requires multidisciplinary care teams and is challenged by data limited to small observational studies and from the high likelihood of side effects of most of the treatments currently used (eg: corticosteroids, methotrexate and TNF-alfa inhibitors).

Interleukin-1 (IL-1) is the prototypical pro-inflammatory cytokine, also referred to as master regulator of the inflammatory response, involved in virtually every acute process. There is evidence that IL-1 plays a role in mouse model of sarcoidosis and human pulmonary lesions as the presence of the inflammasome in granulomas of the heart of patients with cardiac sarcoidosis, providing additional support for a role of IL-1 in the pathogenesis of CS. However, IL-1 blockade has never been evaluated as a potential therapeutic agent for cardiac sarcoidosis.

In the current study, researchers aim to evaluate the safety and efficacy of IL-1 blockade with anakinra (IL-1 receptor antagonist) in patients with cardiac sarcoidosis.

Description

Researchers will perform an open label randomized clinical trial of anakinra (recombinant IL-1 receptor antagonist, Kineret, SOBI, Sweden) given for 4 weeks in 28 patients with cardiac sarcoidosis (defined using Heart Rhythm Society diagnostic criteria).

Eligibility

INCLUSION CRITERIA (all 3 criteria need to be met)

• Clinical diagnosis of cardiac sarcoidosis according to the Heart Rhythm Society or the New Japanese Cardiac Sarcoidosis Guidelines (must meet one of the diagnostic pathways)
• Heart Rhythm Society Diagnostic Criteria based on 2 diagnostic pathways:
  1. Histological diagnosis from myocardial tissue - cardiac sarcoidosis is diagnosed in the presence of non-caseating granuloma on histologic examination of myocardial tissue with no alternative cause identified (including negative stain for microorganisms - as applicable);
  2. Clinical diagnosis from invasive and/or non-invasive studies - it is probable that there is cardiac sarcoidosis if there is (a) histological diagnosis of extracardiac sarcoidosis and (b) one or more of the following: steroid +/- immunosuppressant responsive cardiomyopathy or heart block; unexplained reduction in LVEF (<40%); unexplained sustained (spontaneous or induced) ventricular tachycardia; Mobitz type II 2nd degree or 3rd degree AV block; patchy uptake on dedicated cardiac PET (in a pattern consistent with cardiac sarcoidosis); late gadolinium enhancement on cardiac magnetic resonance (in a pattern consistent with cardiac sarcoidosis); positive gallium uptake (in a pattern consistent with cardiac sarcoidosis) and (c) other causes for the cardiac manifestation(s) have been reasonable excluded.
• Japanese Cardiac Sarcoidosis Diagnostic Criteria:
  1. Histological diagnosis group (those with positive myocardial biopsy findings) Cardiac sarcoidosis is diagnosed histologically when endomyocardial biopsy or surgical specimens demonstrate non-caseating epithelioid granulomas.
  2. Clinical diagnosis group (those with negative myocardial biopsy findings or those not undergoing myocardial biopsy)

The patient is clinically diagnosed as having sarcoidosis:

1. When epithelioid granulomas are found in organs other than the heart and clinical findings strongly suggestive of the above-mentioned cardiac involvement are present (Table 1); or
2. When the patient shows clinical findings strongly suggestive of pulmonary or ophthalmic sarcoidosis; at least 2 of the 5 characteristic laboratory findings of a sarcoidosis (Table 2); and clinical findings strongly suggest the above-mentioned cardiac involvement (Table 1)

        TABLE 1. Clinical findings defining cardiac involvement Cardiac findings should be assess
        based on the major criteria and the minor criteria. Clinical findings that satisfy the
        following 1) or 2) strongly suggest the presence of cardiac involvement.
          1. 2 or more of the 5 major criteria (a)-(e) are satisfied.
          2. 1 of the 5 major criteria (a)-(e) and 2 or more of the 3 minor criteria (f)-(h) are
             satisfied.
        1. Major criteria
          1. High-grade AV block (including complete AV block) or fatal ventricular arrhythmia
             (e.g., sustained VT and VF)
          2. Basal thinning of the ventricular septum or abnormal ventricular wall anatomy
             (ventricular aneurysm, thinning of the middle or upper ventricular septum, regional
             wall thickening
          3. Left ventricular contractile dysfunction (LVEF < 50%)
          4. 67Ga citrate scintigraphy or 18F-FDG PET reveals abnormally high tracer accumulation
             in the heart
          5. Gadolinium-enhanced MRI revealed delayed contrast enhancement of the myocardium 2.
             Minor criteria
          6. Abnormal ECG findings: Ventricular arrhythmias (nonsustained VT, multifocal or
             frequent premature ventricular contractions, bundle branch block, axis deviation, or
             abnormal Q waves
          7. Perfusion defects on myocardial perfusion scintigraphy (SPECT)
          8. Endomyocardial biopsy: Monocyte infiltration and moderate or severe myocardial
             interstitial fibrosis
        Table 2. Characteristic laboratory findings of sarcoidosis 6. Bilateral hilar
        lymphadenopathy 7. High serum angiotensin-converting (ACE) activity or elevated serum
        lysozyme levels 8. High serum soluble interleukin-2 receptor (sIL-2R) levels 9. Significant
        tracer accumulation in 67Ga citrate scintigraphy or 18F-FDG PET 10. A high percentage of
        lymphocytes with a CD4CD8 ration of >3.5 in BAL fluid. 11.
          -  Diagnostic guidelines for isolated cardiac sarcoidosis based on New CS Guidelines in
             Japan Prerequisite
               1. No clinical findings characteristic of sarcoidosis are observed in any organs
                  other than the heart. (The patient should be examined in detail for respiratory,
                  ophthalmic, and skin involvement of sarcoidosis. When the patient is symptomatic,
                  other etiologies that can affect the corresponding organs must be ruled out.)
               2. 67Ga scintigraphy or 18F-FDG PET reveals no abnormal tracer accumulation in any
                  organs other than the heart.
               3. A chest CT scan reveals no shadow along the lymphatic tracts in the lungs or no
                  hilar and mediastinal lymphadenopathy (minor axis>10 mm).
               1. Histological diagnosis group Isolated cardiac sarcoidosis is diagnosed
                  histologically when endomyocardial biopsy or surgical specimens demonstrate
                  non-caseating epithelioid granulomas.
               2. Clinical diagnosis group Isolated cardiac sarcoidosis is diagnosed clinically
                  when criterion (d) and at least 3 other major criteria (a)-(e) are satisfied.
                  (Table 1)
          -  Cardiac fluoro-deoxyglucose uptake on recent PET (performed within the prior month).
          -  CRP high-sensitivty assay >2 mg/l.
        EXCLUSION CRITERIA (any of the following criteria would result in exclusion)
          1. Age<21 years;
          2. Pregnancy;
          3. Inability to obtain consent from patient or legally authorized representative;
          4. Contraindications to treatment with Anakinra (Kineret)(i.e. prior allergic reaction to
             the drug or to E. coli derived products or severe allergy to latex);
          5. Severe anemia (Hgb<8 g/dl - due to the need of more frequent blood sampling with this
             study).
          6. Acute or chronic active infections (not including treated/cured HCV with negative
             viral load).
          7. Acute or chronic inflammatory disease or immunosuppressive therapies (excluding stable
             [>1 month] oral corticosteroids at a dose of prednisone less than 0.5 mg/kg/day or
             methotrexate).
          8. Active acute or chronic psychiatric illness that in the opinion of the investigator
             may prevent from complying with study instructions;
          9. Limited English Proficiency that in the opinion of the investigator may prevent from
             understanding the content of the informed consent form or safely completing the study
             procedures.
         10. Live vaccination within the prior month
         11. Neutropenia (defined as absolute neutrophil count < 1,500/ml or <1,000/ml if subject
             is African American)
         12. History of malignancy within the prior 5 years (with exception of basal cell skin
             cancer, carcinoma in-situ of the cervix or low risk prostate cancer after curative
             therapy)
         13. Participation in another concurrent intervention study within 30 day or treatment with
             an investigational drug within 5 half-lives prior to randomization
         14. Severe kidney disease (GFR <30 mL/min/1.73m2)
         15. Evidence of COVID-19 within the last 60 days or recent (21 days) exposure to close
             personal contact with COVID-19.
         16. [Chronic, moderate-to-severe kidney disease (GFR <60 mL/min/1.73m2) or acute kidney
             injury, or history of severe hypersensitivity reactions to gadolinium-based contrast
             agents] - For VCU Imaging Substudy