Immune Thrombocytopenic Purpura Clinical Trial
Official title:
Treatment of thromBocytopenia With EltRombopag or Intravenous Immune Globulin (IVIG) Before and DurING Invasive Procedures in Patients With Immune ThrombocytoPenia- BRIDGING ITP Study
This is a study to investigate if eltrombopag can be used instead of Intravenous Immune Globulin (IVIG) in patients with ITP, to adequately raise their platelet count when they undergo minor or major surgery. Eltrombopag is a daily, oral pill approved for treatment of ITP. IVIG is a blood product frequently used to treat ITP. Patients with ITP who need surgery have to get treatment to increase their platelet count. IVIG is commonly used for this purpose but eltrombopag may be more effective and convenient for patients.
Immune thrombocytopenia (ITP) is a heterogeneous autoimmune disease characterized by the
presence of platelet autoantibodies, low platelet counts and an increased risk of bleeding.
TPO receptor agonists which stimulate platelet production have been shown to be remarkably
effective in ITP. Their use as a short-term means of elevating platelet counts in preparation
for surgical procedures has not yet been adequately evaluated.
Many patients with moderate to severe ITP (platelet count less than 50 x 10exp9/L) have
stable platelet counts and do not bleed; however, when surgeries or invasive procedures
become necessary, additional treatment is often required to increase the platelet count to
achieve adequate hemostasis. Although specific guidelines for surgical platelet count
thresholds in ITP are lacking, platelet transfusion guidelines recommend a platelet count of
50 - 100 x10exp9/L for the vast majority of surgical procedure; 50x10exp9/L is a typical
threshold for minor surgeries like tooth extractions and endoscopies; and 100x10exp9/L is
used for major surgery like cardiac surgery or neurosurgery.
Commonly, intravenous immunoglobulin (IVIG) is used to rapidly increase platelet counts in
ITP patients before an invasive procedure. IVIG is associated with a transient platelet count
response in approximately 80% of patients, which occurs within 2 - 4 days. In most patients,
platelet counts remain elevated for approximately 4 weeks, allowing enough time to complete
the procedure and for adequate post-operative hemostasis. However, IVIG is a
resource-intensive and expensive blood product associated with frequent side effects.
Eltrombopag is a small molecule, non-peptide thrombopoietin (TPO) receptor agonist indicated
for the treatment of thrombocytopenia in patients with chronic ITP who have had an
insufficient response to corticosteroids, immunoglobulins, or splenectomy. TPO receptor
agonists are an effective new class of medications that are non-immunogenic agonists of the
TPO receptor (c-Mpl) and work by increasing platelet production in ITP patients. In
randomized controlled trials, eltrombopag maintenance therapy has been shown to raise the
platelet count in 60 - 80% of ITP patients and platelet counts generally remain elevated as
long as the drug is continued. Time to response is 1 - 2 weeks with minimal need for dose
titration. Side effects of eltrombopag observed in clinical studies included elevation of
liver enzymes (approximately 10% of patients). The risk of thrombosis and bone marrow
reticulin formation remain uncertain.
The investigators propose a randomized controlled trial (RCT) involving 74 patients (across
approximately 8 centers) in Canada. This study will evaluate the efficacy and safety of
eltrombopag bridging therapy compared with IVIG bridging therapy in adult patients with ITP
who require surgery. This study will also evaluate bleeding, adverse events and
patient-reported treatment satisfaction using the Treatment Satisfaction Questionnaire for
Medication (TSQM). Patients will be stratified according to centre and surgery type (major
vs. minor).
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