Efficacy of Prolonged Anticoagulation for Primary Prevention of Venous Thromboembolic Disease in Autoimmune Hemolytic Anemia: a Prospective, Phase II, Randomized, Multicenter Study

Last updated: January 21, 2025
Sponsor: Centre Hospitalier Universitaire Dijon
Overall Status: Active - Recruiting

Phase

2

Condition

Anemia

Lupus

Venous Thromboembolism

Treatment

treatment "standard"

treatment "intervention"

biological assessment

Clinical Study ID

NCT05089227
AUDIA PHRCI 2019
  • Ages > 18
  • All Genders

Study Summary

Autoimmune hemolytic anemia (AIHA) is a rare autoimmune disease (incidence <1/100,000 population) responsible for the destruction of red blood cells by the host immune system, notably through the action of autoantibodies.

Apart from complications related to anemia, the occurrence of venous thromboembolism (VTE) in this population is frequent, estimated at 20-27%. The risk of VTE is highest during the period of hemolysis, especially during the first 3 months after the diagnosis of AIHA. This risk is 7.5 [4.7; 12.0] times greater than in the general population. No clinical predictive factor for VTE was identified and the usual factors (cancer, previous VTE, bed rest >3 days, surgery, age >70 years, heart or respiratory failure, myocardial infarction, stroke, obesity, hormone replacement therapy) were not considered. Several biological risk factors have been suggested (depth of anemia, bilirubin level, leukocyte count, antiphospholipid antibodies) but have not been confirmed in other studies.

AIHA is therefore a risk factor for VTE in its own right, and the National Diagnostic and Care Protocol (NDCP) recommends the implementation of VTE prevention during acute hemolysis (Grade C). However, the value of this prophylaxis has never been prospectively evaluated and its duration is empirical. In practice, low-molecular-weight heparin (LMWH) is generally used during "flare-ups" of AIHA (diagnosis and relapse) in hospitalized patients, but is rarely continued beyond the hospital phase when VTE also occurs in ambulatory patients.

Thus, we hypothesize that prolonged preventive anticoagulation during the 12-week risk period following diagnosis or relapse of AIHA could decrease the incidence of VTE.

In orthopedic surgery, this strategy has been proven to decrease VTE from 50% to 10-15%. In certain high-risk medical situations, prolonged prophylaxis with apixaban has been shown to decrease the occurrence of VTE from 10.2% to 4.2% in solid cancers4 and from 4-11% to 2% in myeloma.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patient aged ≥ 18 years

  • Patient with a diagnosis of primary or secondary autoimmune hemolytic anemia (AIHA) (infections, hematologic diseases, systemic diseases), according to the followingcriteria:

  • Hemoglobin <12 g/dL

  • and decreased haptoglobin (<0.4 g/L)

  • and positive direct antiglobulin test (direct Coombs test) (IgG +/- C3d)

  • Patient newly diagnosed or relapse

  • Patient with an estimated life expectancy of more than 6 months

  • Patient who provided free, written and informed consent

Exclusion

Exclusion Criteria:

  • Patients with immediate symptomatic VTE, confirmed by appropriate complementaryexaminations (venous Doppler of the lower limbs, thoracic angioscanner or pulmonaryscintigraphy).

  • Patients on curative anticoagulation (venous thromboembolic disease, atrialfibrillation)

  • Patient on dual antiaggregation treatment

  • Patient with active bleeding

  • Patient with a known condition or lesion at risk of bleeding

  • Patient with ischemic stroke with hemorrhagic transformation within 6 months priorto inclusion

  • Patient on preventive anticoagulation for 14 days or more

  • Patient with a contraindication to apixaban:

  • Known hypersensitivity to the molecule or to any of the excipients,,

  • thrombocytopenia <100 G/L,

  • kidney failure (glomerular filtration rate < 30 ml/min/1.73m²)

  • Active liver disease (liver failure defined as Factor V <50% or INR >1.5, ALTelevation >2 times the upper limit of normal)

  • Patients receiving concomitant CYP3A4 inducers (rifampin, phenytoin, carbamazepine,phenobarbital, St. John's Wort) or CYP3A4 inhibitors (azole antifungals, HIVprotease inhibitors), if these therapies cannot be discontinued or modified

  • Patients with a contraindication to enoxaparin:

  • allergy to the drug

  • history of heparin-induced thrombocytopenia

  • Patient with cold agglutinin-related AHAI (C3d-positive ADT alone withidentification of cold agglutinins)

  • Patient with severe disorders of hemostasis:

  • hypofibrinogenemia < 2 g/L,

  • disseminated intravascular coagulation (APTT prolongation>1.2, and PT<50%, andthrombocytopenia<100 G/L, and D-Dimer >500 µg/L)

  • hemophilia

  • Patient whose clinical condition requires hospitalization in an intensive care unit

  • Patient who has already participated in the study

  • Patient not affiliated to national health insurance

  • Patient under legal protection (curatorship, guardianship)

  • Patient subject to a measure of legal protection

  • Pregnant, parturient or breastfeeding women

  • Patient with physiological capacity to procreate (having had her first menstrualperiod and not menopausal and not presenting permanent sterility (hysterectomy,bilateral salpingectomy, bilateral oophorectomy)) and unable to have effectivecontraception (i.e., provided by an estrogen-progestin oral contraceptive orprogestogen, a contraceptive implant, an intrauterine device or a tubal ligation)

  • Patient of legal age who is unable to provide consent

Study Design

Total Participants: 72
Treatment Group(s): 3
Primary Treatment: treatment "standard"
Phase: 2
Study Start date:
February 03, 2022
Estimated Completion Date:
August 31, 2028

Connect with a study center

  • Chu Dijon Bourgogne

    Dijon, 21000
    France

    Active - Recruiting

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