Efficacy and Safety of rhTPO for the Treatment of Thrombocytopenia After Chemotherapy in AML Patients

A Clinical Trial to Evaluate the Efficacy and Safety of Recombinant Human Thrombopoietin in the Treatment of Thrombocytopenia After Chemotherapy in Acute Myeloid Leukemia

In this single-center, randomized, open-label, crossover, prospective clinical trial, a total of 120 AML patients who achieved remission will be randomized into two groups, of 60 cases in each group. Each subject is required to undergo two cycles of chemotherapy. At the treatment cycle, patients received subcutaneous injection of rhTPO. At the control cycle, rhTPO therapy is not given.The safety of rhTPO is evaluated by the monitoring of liver and renal functions, blood coagulation, and TPO-neutralizing antibody, and adverse events associated with rhTPO treatment are recorded during the study period.

Study Overview

• Status: Completed
• Conditions: Thrombocytopenia
• Intervention / Treatment: Drug: recombinant human thrombopoietin

Detailed Description

In this single-center, randomized, open-label, crossover, prospective clinical trial, a total of 120 AML patients who achieved remission following induction chemotherapy will be recruited and randomized into two groups, of 60 cases in each group. For one group, the treatment cycle is in the first chemotherapy cycle and the control cycle is in the second one. For another group, the treatment cycle is in the second chemotherapy cycle and the control cycle is in the first one.

Each subject is required to undergo two cycles of chemotherapy. At the treatment cycle, patients received subcutaneous injection of rhTPO at a dose of 300 U/kg body weight once daily at a platelet count of < 50×109/L, and rhTPO treatment ceased at a platelet count of ≥20×109/L if platelet is not transfused. At the control cycle, rhTPO therapy is not given.

Each subject is required to be followed up for successive two chemotherapy cycles following inclusion in this study. During the follow-up period, routine blood test is performed once every other day, and platelet transfusion is recorded.

The safety of rhTPO is evaluated by the monitoring of liver and renal functions, blood coagulation, and TPO-neutralizing antibody, and adverse events associated with rhTPO treatment are recorded during the study period.

• Study Type: Interventional
• Enrollment (Actual): 58
• Phase: Phase 4

Contacts and Locations

Study Locations

• China
  • Tianjin
    • Tianjin, Tianjin, China, 300020
      • Institute of Hematology & Blood Diseases Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 55 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Age of 18-55 years;
2. Patients that meet the diagnostic criteria of acute myeloid leukemia (except M3 and M7 subtypes), and achieve complete remission following induction chemotherapy and undergo consolidation therapy;
3. Patients who require two successive cycles of DA (Ara-c 1.5 g/m2/q12 h and DNR 40 mg/m2/d on days 1-3) or MA regimen (Ara-C 1.5 g/m2/q12 h and MTZ 6 mg/m2/d on days 1-3) at the phase of consolidation therapy, or underwent consolidation therapy with administration of Ara-C 3 g/m2/q12 h alone, with dose adjustment of less than 10% Ara-C dose;
4. Patients with the minimum platelet count of < 30´109/L at the final cycle of chemotherapy during the induction stage;
5. Patients without apparent liver or renal dysfunctions (serum levels of urea nitrogen, creatinine, aminotransferase and bilirubin were all ≤ 1.5 times of the normal upper limit);
6. Patients without severe heart or lung dysfunctions;
7. Patients with life expectancy of > 12 weeks;
8. Patients with ECOG score of ≤ 2;
9. Patients are willing to participate in the study and sign the informed consent.

Exclusion Criteria:

1. Patients with a medical history of severe allergy to biologics;
2. Patients with thromboembolic or hemorrhagic disease, or a recent medical history of thrombosis;
3. Patients with a history of mental disorders;
4. Pregnant or lactating patients, or patients with failure in use of contraception during the study period;
5. Patients with M3 or M7 subtype;
6. Patients with a platelet count of 1000 ´109/L at the start of the study;
7. Patients with other factors which were considered not to be suitable to participate in the study by the investigators.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Arm A; At the first chemotherapy cycle (treatment cycle), patients receive recombinant human thrombopoietin treatment. At the second chemotherapy cycle (control cycle), recombinant human thrombopoietin therapy is not given.	Drug: recombinant human thrombopoietin; Patients received subcutaneous injection of recombinant human thrombopoietin at a dose of 300 U/kg body weight once daily at a platelet count of < 50×109/L, and recombinant human thrombopoietin treatment ceased at a platelet count of ≥20×109/L if platelet is not transfused.; Other Names: rhTPO
Experimental: Arm B; At the first chemotherapy cycle (control cycle), recombinant human thrombopoietin therapy is not given; at the second chemotherapy cycle (treatment cycle), patients receive recombinant human thrombopoietin treatment.	Drug: recombinant human thrombopoietin; Patients received subcutaneous injection of recombinant human thrombopoietin at a dose of 300 U/kg body weight once daily at a platelet count of < 50×109/L, and recombinant human thrombopoietin treatment ceased at a platelet count of ≥20×109/L if platelet is not transfused.; Other Names: rhTPO

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Duration of platelet count of < 20 ´ 109/Lat each cycle of chemotherapy.	From Day1 after chemotherapy up to Day21 after chemotherapy

Secondary Outcome Measures

Outcome Measure	Time Frame
Time and dose of platelet transfusion at each cycle of chemotherapy	From Day1 after chemotherapy up to Day21 after chemotherapy
The minimum platelet count at each cycle of chemotherapy	From Day1 after chemotherapy up to Day21 after chemotherapy
Duration from the minimum platelet count to ≥ 20´109/L at each cycle of chemotherapy according to CTCAE(v4.0)	From Day1 after chemotherapy up to Day21 after chemotherapy
Number and grade of bleeding Adverse Events at each cycle of chemotherapy	From Day1 after chemotherapy up to Day21 after chemotherapy
Duration of hospital stay (from the first day of chemotherapy to discharge from hospital) at each cycle of chemotherapy	From Day1 after chemotherapy up to Day21 after chemotherapy

Collaborators and Investigators

• Sponsor: Institute of Hematology & Blood Diseases Hospital

Study record dates

Study Major Dates

• Study Start (Actual): October 1, 2014
• Primary Completion (Actual): August 1, 2018
• Study Completion (Actual): August 31, 2018

Study Registration Dates

• First Submitted: October 9, 2014
• First Submitted That Met QC Criteria: October 15, 2014
• First Posted (Estimate): October 20, 2014

Study Record Updates

• Last Update Posted (Actual): March 20, 2020
• Last Update Submitted That Met QC Criteria: March 19, 2020
• Last Verified: March 1, 2020

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Hematologic Diseases; Blood Platelet Disorders; Thrombocytopenia
• Other Study ID Numbers: IHBDH-IIT2014010

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No