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A Trial of Eltrombopag or Intravenous Immune Globulin Before Surgery for Immune Thrombocytopenia Patients

Primary Purpose

Immune Thrombocytopenic Purpura

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Eltrombopag
IVIG infusion
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Immune Thrombocytopenic Purpura focused on measuring Thrombocytopenia, ITP, Platelets, Bleeding, Immune, Eltrombopag, IVIG

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary or secondary ITP;
  • Platelet count below surgical platelet count threshold (50 x10^9/L for minor surgery; 100 x 10^9/L for major surgery);
  • 18 years of age or older;
  • On stable doses of concomitant ITP medications (i.e the dose administered has not changed) or no ITP medication for at least 2 weeks;
  • At least 3-weeks lead time available between randomization and scheduled surgery;
  • IVIG and Eltrombopag are acceptable ITP treatment options for this patient;
  • Able to provide informed consent.

Exclusion Criteria:

  • Pregnancy or breastfeeding;
  • Treatment with IVIG within the last 2 weeks;
  • Treatment with a thrombopoietin receptor agonist (eltrombopag or romiplostim) within the last 4 weeks;
  • AST, ALT above 2X upper limit of normal;
  • Bilirubin above 1.5X upper limit of normal in the absence of clinically benign liver disorder (eg. Gilberts syndrome);
  • Deep vein thrombosis, myocardial infarction, thrombotic stroke or arterial thrombosis in the last 12 months;
  • History of bone marrow reticulin or fibrosis;
  • Known liver cirrhosis;
  • Active malignancy (defined as requiring treatment or palliation within the last 6 months);
  • Any additional laboratory test result, health related illness or other diagnosis which, in the opinion of the treating physician, may put the subject's health or safety at risk.

Sites / Locations

  • University of Alberta Hospital
  • Vancouver General Hospital
  • Hamilton Health Sciences
  • London Health Sciences Center
  • Ottawa Hospital
  • Sunnybrook Hospital
  • St.Micheal's Hospital
  • Hopital Maisonneuve-Rosemont
  • Jewish General Hospital
  • The Haga Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Eltrombopag

IVIG infusion

Arm Description

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.

Intravenous immunoglobulin (IVIG) is used to rapidly increase platelet counts in ITP patients. IVIG is associated with a transient platelet count response in approximately 80% of patients, which occurs within 2 - 4 days. It is commonly used to improve platelet count numbers prior to surgery for patients with ITP.

Outcomes

Primary Outcome Measures

Achievement of a platelet count level that is above the platelet count threshold for surgery preoperatively and that is maintained above the threshold during the post-hemostasis period without the use of rescue treatment
Threshold is a platelet count of 50 x 10^9/L for minor surgery and 100 x 10^9/L for major surgery.

Secondary Outcome Measures

Time to treatment failure
Time to the occurrence of a platelet count level below the designated threshold, or the administration of rescue treatment
Surgical delays or cancellations
Proportion of patients with surgical delays or cancellations
Bleeding
Graded as per the ITP bleeding score
Thrombocytosis
Platelet count >400 x 10^9/L
Blood product transfusions
Proportion of patients requiring platelet, red blood cells and plasma transfusions
Rescue treatment
New ITP treatment (typically platelet transfusions, high dose IVIG or high dose corticosteroids) or an increased dose of existing ITP treatment administered to increase platelet counts above threshold
Platelet count change over time
Trend of all platelet count measurements in the trial
Patient satisfaction with treatment
Assessed using the Treatment Satisfaction Questionnaire for Medications Score vII (which incorporates effectiveness, convenience, side effects, and overall satisfaction)
Hospitalizations
Unanticipated admissions to hospital or prolongation of hospitalization
Thrombosis
Symptomatic thrombotic events confirmed with diagnostic imaging
Adverse Events
Defined using the Common Terminology Criteria for Adverse Events v3.0

Full Information

First Posted
June 12, 2012
Last Updated
September 4, 2020
Sponsor
McMaster University
Collaborators
GlaxoSmithKline, Hamilton Health Sciences Corporation, Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT01621204
Brief Title
A Trial of Eltrombopag or Intravenous Immune Globulin Before Surgery for Immune Thrombocytopenia Patients
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
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
October 2012 (Actual)
Primary Completion Date
June 2019 (Actual)
Study Completion Date
August 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McMaster University
Collaborators
GlaxoSmithKline, Hamilton Health Sciences Corporation, Novartis

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Immune Thrombocytopenic Purpura
Keywords
Thrombocytopenia, ITP, Platelets, Bleeding, Immune, Eltrombopag, IVIG

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
74 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Eltrombopag
Arm Type
Experimental
Arm Description
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.
Arm Title
IVIG infusion
Arm Type
Active Comparator
Arm Description
Intravenous immunoglobulin (IVIG) is used to rapidly increase platelet counts in ITP patients. IVIG is associated with a transient platelet count response in approximately 80% of patients, which occurs within 2 - 4 days. It is commonly used to improve platelet count numbers prior to surgery for patients with ITP.
Intervention Type
Drug
Intervention Name(s)
Eltrombopag
Other Intervention Name(s)
Revolade
Intervention Description
Participants are started on 50mg daily oral pill (or 25mg daily for patients of East Asian descent) 21 days before surgery. Dose may be adjusted based on subsequent platelet counts (minimum 25mg; maximum 75mg).
Intervention Type
Drug
Intervention Name(s)
IVIG infusion
Other Intervention Name(s)
Intravenous Immunoglobulin, IgG
Intervention Description
IVIG infusion (1-2 g/kg) given 7 (+/-2) days prior to surgery; with an additional infusion allowed within one week of achievement of surgical hemostasis, if needed
Primary Outcome Measure Information:
Title
Achievement of a platelet count level that is above the platelet count threshold for surgery preoperatively and that is maintained above the threshold during the post-hemostasis period without the use of rescue treatment
Description
Threshold is a platelet count of 50 x 10^9/L for minor surgery and 100 x 10^9/L for major surgery.
Time Frame
For a the period of time from the final pre-operative visit until 7 days after surgical hemostasis is achieved
Secondary Outcome Measure Information:
Title
Time to treatment failure
Description
Time to the occurrence of a platelet count level below the designated threshold, or the administration of rescue treatment
Time Frame
During the period from the final pre-operative visit until 7 days after surgical hemostasis is achieved
Title
Surgical delays or cancellations
Description
Proportion of patients with surgical delays or cancellations
Time Frame
Measured at time of planned surgery
Title
Bleeding
Description
Graded as per the ITP bleeding score
Time Frame
During treatment and follow up (on average, 8 weeks from starting treatment)
Title
Thrombocytosis
Description
Platelet count >400 x 10^9/L
Time Frame
During treatment and follow up (on average, 8 weeks from starting treatment)
Title
Blood product transfusions
Description
Proportion of patients requiring platelet, red blood cells and plasma transfusions
Time Frame
During treatment and follow up (on average, 8 weeks from starting treatment)
Title
Rescue treatment
Description
New ITP treatment (typically platelet transfusions, high dose IVIG or high dose corticosteroids) or an increased dose of existing ITP treatment administered to increase platelet counts above threshold
Time Frame
During the period from the final pre-operative visit until 7 days after surgical hemostasis is achieved
Title
Platelet count change over time
Description
Trend of all platelet count measurements in the trial
Time Frame
During treatment and follow up (on average, 8 weeks from starting treatment)
Title
Patient satisfaction with treatment
Description
Assessed using the Treatment Satisfaction Questionnaire for Medications Score vII (which incorporates effectiveness, convenience, side effects, and overall satisfaction)
Time Frame
Immediately before surgery (final pre-op visit) and 7 days (+/- 2 days) after surgical hemostasis is achieved
Title
Hospitalizations
Description
Unanticipated admissions to hospital or prolongation of hospitalization
Time Frame
During treatment and follow up (on average, 8 weeks from starting treatment)
Title
Thrombosis
Description
Symptomatic thrombotic events confirmed with diagnostic imaging
Time Frame
During treatment and follow up (on average, 8 weeks from starting treatment)
Title
Adverse Events
Description
Defined using the Common Terminology Criteria for Adverse Events v3.0
Time Frame
During treatment and follow up (on average, 8 weeks from starting treatment)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary or secondary ITP; Platelet count below surgical platelet count threshold (50 x10^9/L for minor surgery; 100 x 10^9/L for major surgery); 18 years of age or older; On stable doses of concomitant ITP medications (i.e the dose administered has not changed) or no ITP medication for at least 2 weeks; At least 3-weeks lead time available between randomization and scheduled surgery; IVIG and Eltrombopag are acceptable ITP treatment options for this patient; Able to provide informed consent. Exclusion Criteria: Pregnancy or breastfeeding; Treatment with IVIG within the last 2 weeks; Treatment with a thrombopoietin receptor agonist (eltrombopag or romiplostim) within the last 4 weeks; AST, ALT above 2X upper limit of normal; Bilirubin above 1.5X upper limit of normal in the absence of clinically benign liver disorder (eg. Gilberts syndrome); Deep vein thrombosis, myocardial infarction, thrombotic stroke or arterial thrombosis in the last 12 months; History of bone marrow reticulin or fibrosis; Known liver cirrhosis; Active malignancy (defined as requiring treatment or palliation within the last 6 months); Any additional laboratory test result, health related illness or other diagnosis which, in the opinion of the treating physician, may put the subject's health or safety at risk.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Donald M Arnold, MD MSc
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alberta Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G2G3
Country
Canada
Facility Name
Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z1M9
Country
Canada
Facility Name
Hamilton Health Sciences
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 3Z5
Country
Canada
Facility Name
London Health Sciences Center
City
London
State/Province
Ontario
ZIP/Postal Code
N6A5W9
Country
Canada
Facility Name
Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H8L6
Country
Canada
Facility Name
Sunnybrook Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N3M5
Country
Canada
Facility Name
St.Micheal's Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B1W8
Country
Canada
Facility Name
Hopital Maisonneuve-Rosemont
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H1T2M4
Country
Canada
Facility Name
Jewish General Hospital
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3T1E2
Country
Canada
Facility Name
The Haga Hospital
City
The Hague
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
32853584
Citation
Arnold DM, Heddle NM, Cook RJ, Hsia C, Blostein M, Jamula E, Sholzberg M, Lin Y, Kassis J, Larratt L, Tinmouth A, Amini S, Schipperus M, Lim W, Vishnu P, Warner M, Carruthers J, Li N, Lane S, Kelton JG. Perioperative oral eltrombopag versus intravenous immunoglobulin in patients with immune thrombocytopenia: a non-inferiority, multicentre, randomised trial. Lancet Haematol. 2020 Sep;7(9):e640-e648. doi: 10.1016/S2352-3026(20)30227-1.
Results Reference
result
PubMed Identifier
30685874
Citation
Arnold DM, Jamula E, Heddle NM, Cook RJ, Hsia C, Sholzberg M, Lin Y, Kassis J, Blostein M, Larratt L, Amini S, Schipperus M, Carruthers J, Lane SJ, Li N, Kelton JG. Peri-Operative Eltrombopag or Immune Globulin for Patients with Immune Thrombocytopaenia (The Bridging ITP Trial): Methods and Rationale. Thromb Haemost. 2019 Mar;119(3):500-507. doi: 10.1055/s-0038-1677531. Epub 2019 Jan 27.
Results Reference
derived

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A Trial of Eltrombopag or Intravenous Immune Globulin Before Surgery for Immune Thrombocytopenia Patients

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