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Therapeutic Plasma Exchange, Rituximab and IV Ig for Severe Acute Exacerbation of IPF Admitted in ICU

Not Applicable
Conditions
Exacerbation of Idiopathic Pulmonary Fibrosis
Interventions
Other: Conventional treatment of AE-IPF
Other: Therapeutic plasma exchanges
Registration Number
NCT03584802
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

Idiopathic pulmonary fibrosis (IPF) is a fibroproliferative, irreversible disease of unknown cause, occurring mainly in patients older than 50. IPF is a rare but fatal lung disease, with an estimated prevalence of 14 to 28/100000 and a median survival time of 3 years. Acute exacerbation of IPF (AE-IPF) is a major event of IPF, as it is responsible for the death of 30-50 % of IPF patients; its annual incidence varies between 5 and 10%. The current literature indicates that IPF is associated with the development of an auto-immunity process targeting epithelial and endothelial lung cells. Autoantibodies have been associated with a poorer prognosis. A study by DONAHOE et al. (Plos One, 2015) indicates that the combination of corticosteroids, plasma exchanges, rituximab and immunoglobulins may improve the prognosis of the most severe forms of AE-IPF. In that study, the observed survival rate in patients receiving this combination of treatment was 70% as compared with 20% in historical controls. This therapeutic combination approach is designed both to eliminate and inhibit the production of circulating antibodies targeting the lungs. Considering the high mortality rate of an AE-IPF episode and the potential benefit of such an original approach, a well-conducted randomized controlled trial is critical.

Detailed Description

Idiopathic pulmonary fibrosis (IPF) is a fibroproliferative, irreversible disease of unknown cause, occurring mainly in patients older than 50. IPF is a rare but fatal lung disease, with an estimated prevalence of 14 to 28/100000 and a median survival time of 3 years. Acute exacerbation of IPF (AE-IPF) is a major event of IPF, as it is responsible for the death of 30-50 % of IPF patients; its annual incidence varies between 5 and 10%. The current literature indicates that IPF is associated with the development of an auto-immunity process targeting epithelial and endothelial lung cells. Autoantibodies have been associated with a poorer prognosis. A study by DONAHOE et al. (Plos One, 2015) indicates that the combination of corticosteroids, plasma exchanges, rituximab and immunoglobulins may improve the prognosis of the most severe forms of AE-IPF. In that study, the observed survival rate in patients receiving this combination of treatment was 70% as compared with 20% in historical controls. This therapeutic combination approach is designed both to eliminate and inhibit the production of circulating antibodies targeting the lungs. Considering the high mortality rate of an AE-IPF episode and the potential benefit of such an original approach, a well-conducted randomized controlled trial is critical.

The main objective is to evaluate the impact on overall mortality at day 28 of plasma exchanges, rituximab, intravenous immunoglobulins (IVIg), and corticosteroid administration versus standard corticosteroid therapy in hypoxemic patients admitted in ICU for severe acute exacerbation of idiopathic pulmonary fibrosis.

The primary assessment criterion will be overall mortality at day 28 after initiation of therapy (Day 1).

Secondary objectives are the following:

1. Efficacy:

1.1. To compare the overall mortality at day 90, at 6 months and at 12 months after the initiation of therapy 1.2. To compare the exposition to mechanical ventilation 1.3. To compare the length of ICU and hospital-stay 1.4. To compare the evolution of Sequential Organ Failure Assessment (SOFA) score 1.5. To compare the radiological evolution 1.6. To compare the evolution of lung injury biomarkers in plasma 1.7. To compare the changes in circulating autoantibodies levels before and after therapy 1.8. To compare the evolution of blood fibrocytes proportion 1.9. To evaluate respiratory functional at 3 months and compare data previously available.

1.10. To assess quality of life (SF36), autonomy (ADL) and muscle strength scores (MRC) at 3 months of inclusion (Cf annexe)

2. Safety:

2.1. To compare the occurrence of healthcare-associated infection 2.2. To describe the specific complications associated to the experimental treatment

Secondary assessment criteria are the following:

3. Efficacy:

3.1. Overall mortality at day 90, at 6 months and at 12 months 3.2. Number of days alive without mechanical ventilation between inclusion and day 28 3.3. Length of ICU-stay and hospital-stay 3.4. Changes in SOFA score from D1 to D3, D7, D16, D21, D28 or discharge-day from ICU as appropriate 3.5. Variation of global extent of High Resolution Computed Tomography (HRCT) infiltrates between initial HRCT and D90 3.6. Changes in lung injury plasmatic biomarkers (KL-6, SP-D) from D1 to D16, D21, D28 and D90 3.7. Changes in circulating antibodies levels (anti-periplakin, anti-HSP70 and anti-vimentin antibodies) from D1 to D28 and D90 3.8. Changes in the proportion of blood fibrocytes from D1 to D16, D28 and D90

4. Safety:

4.1. Proportion of patients with at least one episode of any healthcare-associated infection between inclusion and D28 4.2. The following complications in the experimental group will be described: 4.2.1. Proportion of catheter-linked complications between inclusion and D16 4.2.2. Number of blood units transfused between inclusion and day 28. 4.2.3. Proportion of major bleeding according to the International Society On Thrombosis And Haemostasis 4.2.4. Proportion of patients with occurrence of an acute renal failure at D28, according to the Kidney Disease Improving Global Outcomes (KDIGO) guidelines 4.2.5. Proportion of patients with anaphylactic reaction at day 28

The experimental design is multicenter, randomized, controlled, open-label superiority trial in parallel groups. The population involved is ICU patients with a Partial pressure of oxygen/ Fraction inspired by oxygen (PaO2/FIO2) ratio \< 200 and a diagnosis of acute exacerbation of idiopathic pulmonary fibrosis.

The experimental group will receive a combination of:

1. Methylprednisolone bolus of 1g i.v. day 1, then 20 mg/day (or oral prednisone equivalent) for 21 days;

2. Nine therapeutic plasma exchanges of 1.5x the estimated plasma volumes using albumin:saline (3:1) or fresh frozen plasma in case of an International Normalised Ratio (INR) superior to 1.5, on days 1,2,3,5,7,9,11,13,15; followed by administration of low dose of intravenous immunoglobulin (100 mg/kg)

3. Rituximab 1 g i.v. on days 7 and 15 (after therapeutic plasma exchange and premedication);

4. Intravenous immunoglobulin 0.5 g/kg/d on days 16 to 19.

The reference group will receive:

Intravenous methylprednisolone bolus of 10 mg/kg (max. 1g) on day 1, 2 and 3, then 1 mg/kg/d for 1 week, and 0.75 mg/kg/d for 1 week, then 0.5 mg/kg/d for 1 week, and 0.25 mg/kg/d for 1 week, and 0.125 mg/kg/d until day 90. Shift to oral prednisone as soon as the oral route is available.

Other procedures added by the research:

Blood sampling for serial serum lung injury biomarkers, fibrocytes determination and circulating antibodies measurements

Risks added by the research: C Number of subjects chosen: 40 Number of centres : 17

Research period:

Inclusion period: 36months Length of participation: one year

* Maximum period between selection and inclusion: 3 days

* Treatment period: 90 days

* Follow up period: 1 year +/- 2 weeks

* Total research period: 48 months

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
40
Inclusion Criteria
  1. Patient ≥ 18 years of age

  2. Admitted to ICU in the last 72 h

  3. Definite or probable IPF diagnosis defined on 2018 ATS/ERS/JRS/ALAT guidelines or a possible usual interstitial pneumonia pattern on HRCT without etiology.

  4. Definite AE-IPF according to the 2018 revised criteria :

    1. Previous or concurrent diagnosis of idiopathic pulmonary fibrosis (if the diagnosis of IPF is not previously established, this criterion can be met by the presence of radiologic and or histopathologic changes consistent with usual interstitial pneumonia (UIP) pattern on the current evaluation);
    2. Acute worsening or development of dyspnea typically of less than one-month duration;
    3. Computed tomography with new bilateral ground-glass opacity and/or consolidation superimposed on a background pattern consistent with a UIP pattern (if no previous computed tomography is available, the qualifier "new" can be dropped);
    4. Deterioration not fully explained by cardiac failure or fluid overload.
  5. PaO2/FiO2 ratio < 200 measured on FiO2 1

Exclusion Criteria
  1. Known hypersensitivity intravenous immunoglobulins or rituximab

  2. Severe heart failure

  3. Active and uncontrolled bacterial fungal or parasitic infection ruled out by at least one of these two conditions

    1. Procalcitonin value at inclusion < 0.25 ng/mL OR
    2. Adapted antimicrobial therapy for at least 48 hours at inclusion
  4. Positive multiplex PCR for Influenzae A and B, or VRS

  5. Deep Veinous Thrombosis or Pulmonary embolism in the last six months

  6. Prior exposures to human-murine chimeric antibodies

  7. Ongoing treatment with a cellular immunosuppressant (e.g., cyclophosphamide, methotrexate, mycophenolate, azathioprine, calcineurin inhibitors, etc.)

  8. Subject treated with more than 2 boluses of methylprednisolone (total dose > 500mg of methylprednisolone) or one dose > 10mg/kg in the last 72 hours

  9. Uncorrectable coagulopathies or thrombocytopenia < 30000/mm3

  10. Active cancer (other than basal cell carcinoma of the skin)

  11. Other source of immunosuppression (i.e. HIV infection, solid organ transplant, lymphoma or leukemia)

  12. Pregnancy

  13. Patient listed for lung transplantation

  14. Patient on ECMO

  15. Patient with a do-not-intubate order at inclusion

  16. Concurrent participation in other experimental trials

  17. Not Affiliation to the French social security

  18. Not Written informed consent from the patient or a legal representative if appropriate

  19. Hypersensitivity to corticosteroids, cotrimoxazole / atovaquone

  20. Patients with severe renal insufficiency (creatine clearance <15ml / min)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Conventional treatment of AE-IPFConventional treatment of AE-IPFIntravenous methylprednisolone bolus of 10mg/kg on day1, 2 and 3, then 1mg/kg/d for 1 week, and 0,75 mg/kg/d for 1 week, then 0,5 mg/kg/d for 1 week, and 0,25 mg/kg/d for 1 week, and 0,125 mg/kg/d until day 90. Shift to oral prednisone as soon as the oral route is available.
Experimental treatment of AE-IPFTherapeutic plasma exchangesThe experimental group will receive a combination of: 1- Methylprednisolone bolus of 1g IV day 1, then 20 mg/day (or oral prednisolone equivalent) for 21 days; 2- Nine therapeutic plasma exchanges of 1,5x the estimated plasma volumes using albumin: saline (3:1) or fresh frozen plasma in case of an INR superior to 1,5, on days 1,2,3,5,7,9,11,13,15; followed by administration of low dose of intravenous immunoglobulin (100mg/kg) 3, Rituximab 1g IV on days 7 and 15 (after therapeutic plasma exchange and premedication) 4, Intravenous immunoglobulin 0,5g/kg/d on days 16 to 19,
Primary Outcome Measures
NameTimeMethod
Overall mortality at day 28 after initiation of therapy (Day1)28 days

Overall mortality at day 28 after initiation of therapy (Day1)

Secondary Outcome Measures
NameTimeMethod
Overall mortality at 12 months12 months

Overall mortality at 12 months

Proportion of major bleeding according to the International Society On Thrombosis and Haemostasis28 days

Proportion of major bleeding

Proportion of patients with at least one episode of any healthcare-associated infection between inclusion and day 2828 days

Proportion of patients with at least one episode of any healthcare-associated infection

Proportion of patients with anaphylactic reaction at day 2828 days

Proportion of patients with anaphylactic reaction

Number of days alive without mechanical ventilation between day 1 and day 2828 days

Number of days alive without mechanical ventilation

Variation of global extent of HRCT infiltrates between initial HRCT and Day 90 according to AKIRA et al90 days

Variation of global extent of HRCT infiltrates

Changes in lung injury biomarkers in plasma (KL-6, SP-D) between day 1 and day 9090 days

Changes in lung injury biomarkers in plasma

Proportion of patients with occurrence of an acute renal failure at day 28, according to the KDIGO guidelines28 days

Proportion of patients with occurrence of an acute renal failure

Length of ICU- stay and hospital-stay12 months

Length of ICU- stay and hospital-stay

Changes in circulating autoantibodies levels (anti-periplakin, anti-HSP70 and anti-vimentin antibodies) between day 1 and day 9090 days

Changes in circulating autoantibodies levels

Evolution of the SOFA score between day 1 and day 28 or discharge-day from ICU as appropriate (in case of death before Day 28, the last SOFA score collected will be 24 points)28 days

The Sequential Organ Failure Assessment (SOFA) score is calculated with the combination of 6 scores:

* respiratory score with the parameter PaO2/ FiO2

* neurological score with Mean arterial pressure parameter

* hepatic score with bilirubin parameter

* coagulation score with measure of platelets

* renal score with creatinine parameter

The total score will range to 0 at 24; 0 being the better outcome and 24 the worse.

Changes in the proportion of blood fibrocytes between day 1 and day 9090 days

Changes in the proportion of blood fibrocytes between day 1 and day 90

Proportion of catheter-linked complications between inclusion and day 1616 days

Proportion of catheter-linked complications between inclusion and day 16

Number of blood units transfused between inclusion and day 2828 days

Number of blood units transfused between inclusion and day 28

Trial Locations

Locations (1)

Hôpital Bichat Claude Bernard

🇫🇷

Paris, France

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