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Eltrombopag Used in Thrombocytopenia After Comsolidation Therapy in AML

Primary Purpose

Eltrombopag, Thrombocytopenia, Acute Myeloid Leukemia

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Eltrombopag
Sponsored by
Nanfang Hospital, Southern Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Eltrombopag

Eligibility Criteria

14 Years - 60 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

All patients with the age range from 14 to 60 years old with AML exclusive of APL in CR status; All those accepting IA or DA (IDA 10mg or DNR 45mg/m2, d1-3, Ara-C 2g/m2 q12h, d1-3) or MDAC (Ara-C 2g/m2 q12h, d1-3) as consolidation regimens.

Exclusion Criteria:

Those without obtaining CR; Those experience more 6 cycles of chemotherapy; Any abnormality in a vital sign (e.g., organ function failure, serious infection ); Patients with any conditions not suitable for the trial (investigators' decision).

Sites / Locations

  • Department of Hematology,Nanfang Hospital, Southern Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Eltrombopag treatment

Eltrombopag free

Arm Description

Eltrombopag 25mg bid, starts from the day when platelet count decreases lower than 30×10'9/L, and the treatment lasts for at least 5 days, and stops until platelet count goes up to more than 30×10'9/L, after consolidation therapy in AML patents. Platelet transfusion application is routinely done when platelet count is lower than 20×10'9/L or active hemorrage happens to patients.

Eltrombopag treatment is not performed in this group. Platelet transfusion application is routinely done when platelet count is lower than 20×10'9/L or active hemorrage happens to patients.

Outcomes

Primary Outcome Measures

Thrombocytopenia time
The lasting time for platelet count lower than 20×10'9/L after consolidation therapy.
The incidence of fatal hemorrage
Fatal hemorrage includes all bleedings have life-threaten to the patients, eg. gastrointestinal bleeding, brain bleeding, pneumorrhagia, etc.

Secondary Outcome Measures

The incidence of thrombus
All kinds of thrombus happens in veins and arteries after consolidation therapy.

Full Information

First Posted
October 7, 2018
Last Updated
October 7, 2018
Sponsor
Nanfang Hospital, Southern Medical University
Collaborators
Second Affiliated Hospital, Sun Yat-Sen University, Guangzhou First People's Hospital, Southern Medical University, China, Wuhan General Hospital of Guangzhou Military Command, Third Affiliated Hospital, Sun Yat-Sen University, Dongguan Kanghua Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03701217
Brief Title
Eltrombopag Used in Thrombocytopenia After Comsolidation Therapy in AML
Official Title
Eltrombopag Used in Thrombocytopenia After Comsolidation Therapy in Acute Myeloid Leukemia (AML)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Unknown status
Study Start Date
September 10, 2018 (Actual)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
October 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nanfang Hospital, Southern Medical University
Collaborators
Second Affiliated Hospital, Sun Yat-Sen University, Guangzhou First People's Hospital, Southern Medical University, China, Wuhan General Hospital of Guangzhou Military Command, Third Affiliated Hospital, Sun Yat-Sen University, Dongguan Kanghua Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Eltrombopag has been used in the treatment of immune thrombocytopenia (ITP), and significantly increased platelet count and decreased fatal hemorrage. As it's known that all patients with acute leukemia will experience bone marrow suppression and thrombocytopenia after chemotherapy. Some patients even died of fatal bleeding during this period for lacking of platelet transfusion or platelet transfusion refractoriness. So a lot needs to be done to shortern thrombocytopenia time or reduce fatal hemorrage incidence after chemotherapy in acute leukemia patients. In this prospective randomized controlled study, the effect and safety of eltrombopag in the treatment of thrombocytopenia after consolidation therapy in acute myeloid leukemia (AML) is evaluated.
Detailed Description
Eltrombopag has been used in the treatment of immune thrombocytopenia (ITP), and significantly increased platelet count and decreased fatal hemorrage. As it's known that all patients with acute leukemia will experience bone marrow suppression and thrombocytopenia after chemotherapy. Some patients even died of fatal bleeding during this period for lacking of platelet transfusion or platelet transfusion refractoriness. So a lot needs to be done to shortern thrombocytopenia time or reduce fatal hemorrage incidence after chemotherapy in acute leukemia patients. In this prospective randomized controlled study, the effect and safety of eltrombopag in the treatment of thrombocytopenia after consolidation therapy in acute myeloid leukemia (AML) is evaluated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eltrombopag, Thrombocytopenia, Acute Myeloid Leukemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
220 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Eltrombopag treatment
Arm Type
Experimental
Arm Description
Eltrombopag 25mg bid, starts from the day when platelet count decreases lower than 30×10'9/L, and the treatment lasts for at least 5 days, and stops until platelet count goes up to more than 30×10'9/L, after consolidation therapy in AML patents. Platelet transfusion application is routinely done when platelet count is lower than 20×10'9/L or active hemorrage happens to patients.
Arm Title
Eltrombopag free
Arm Type
Active Comparator
Arm Description
Eltrombopag treatment is not performed in this group. Platelet transfusion application is routinely done when platelet count is lower than 20×10'9/L or active hemorrage happens to patients.
Intervention Type
Drug
Intervention Name(s)
Eltrombopag
Intervention Description
Eltrombopag 25mg bid, starts from the day when platelet count decreases lower than 30×10'9/L, and the treatment lasts for at least 5 days, and stops until platelet count goes up to more than 30×10'9/L, after consolidation therapy in AML patents.
Primary Outcome Measure Information:
Title
Thrombocytopenia time
Description
The lasting time for platelet count lower than 20×10'9/L after consolidation therapy.
Time Frame
30 days after consolidation therapy.
Title
The incidence of fatal hemorrage
Description
Fatal hemorrage includes all bleedings have life-threaten to the patients, eg. gastrointestinal bleeding, brain bleeding, pneumorrhagia, etc.
Time Frame
30 days after consolidation therapy.
Secondary Outcome Measure Information:
Title
The incidence of thrombus
Description
All kinds of thrombus happens in veins and arteries after consolidation therapy.
Time Frame
30 days after consolidation therapy.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients with the age range from 14 to 60 years old with AML exclusive of APL in CR status; All those accepting IA or DA (IDA 10mg or DNR 45mg/m2, d1-3, Ara-C 2g/m2 q12h, d1-3) or MDAC (Ara-C 2g/m2 q12h, d1-3) as consolidation regimens. Exclusion Criteria: Those without obtaining CR; Those experience more 6 cycles of chemotherapy; Any abnormality in a vital sign (e.g., organ function failure, serious infection ); Patients with any conditions not suitable for the trial (investigators' decision).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dan Xu
Phone
+86-20-61641615
Email
xudan2@medmail.com.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dan Xu
Organizational Affiliation
Nanfang Hospital, Southern Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Hematology,Nanfang Hospital, Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510515
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dan Xu
Phone
+86-20-61641615
Email
xudan2@medmail.com.cn

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Eltrombopag Used in Thrombocytopenia After Comsolidation Therapy in AML

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