Trial of Eltrombopag During Consolidation Therapy in Adults With AML in Complete Remission

Acute Myeloid Leukemia Clinical Trial

— PrE0901  

Official title:

Phase I Dose Finding/Phase II Placebo-Controlled Trial of Eltrombopag During Consolidation Therapy in Adults With Acute Myeloid Leukemia (AML) in Complete Remission

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01656252
• Other study ID #: PrE0901
• Secondary ID: ELT114465
• Status: Terminated
• Phase: Phase 1/Phase 2
• Start date: July 2012
• Est. completion date: March 2016

Study information

• Verified date: October 2020
• Source: PrECOG, LLC.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Patients with Acute Myeloid Leukemia (AML) in complete remission will receive eltrombopag while undergoing consolidation chemotherapy with high-dose cytarabine. Eltrombopag may help increase the number of platelets during chemotherapy and may help prevent the risk of bleeding. Phase I will study the side effects, best dose and platelet effects of eltrombopag when given with consolidation chemotherapy. After the maximum safe and tolerated dose and schedule is found in Phase I, the study will proceed to Phase II. Phase II will confirm the dose and schedule of eltrombopag identified in Phase I that can increase platelet counts in patients receiving consolidation therapy.

Description:

Consolidation chemotherapy with high dose cytarabine usually causes myelosuppression for 14 to 21 days after each treatment. Patients have low blood counts for days or weeks before the bone marrow resumes function. This may result in e.g., hospitalization, treatment with antibiotics, and transfusions with blood and/or platelets. In addition, this may cause a delay in treatment and reduction in dose. To achieve the best outcome from treatment, dose reductions and delays in treatment must be avoided. The incidence and duration of decreased white blood cells (neutropenia) and neutropenic complications have been reduced by the use of growth colony stimulating factors. Additionally, the use of erythropoietin-stimulating factors has reduced anemia and the need for red blood cell transfusions. Thrombocytopenia remains an important limiting factor in administration of chemotherapy and maintaining dose intensity in some patients. Additionally, the risk of bleeding secondary to low platelet counts may increase sickness or even death in patients undergoing cancer treatment. Thrombopoietin (TPO) is the principal cytokine involved in the regulation of megakaryopoiesis and platelet production. Eltrombopag is an orally bioavailable, small molecule, TPO-receptor agonist that stimulates platelet production by a similar, but not identical, mechanism to endogenous TPO. Eltrombopag has been approved in the U.S. for the treatment of chronic Idiopathic Thrombocytopenic Purpura. Eltrombopag is also under development for other indications such as Hepatitis C Virus-associated thrombocytopenia, Myelodysplastic Syndrome/AML, and oncology related thrombocytopenias. This agent appears to possess many of the desirable properties for a treatment for chemotherapy induced thrombocytopenia, including oral administration. The Phase I portion of this study will be conducted using a dose escalation/de-escalation strategy for patients in either the first or second complete remission. Dose escalations are planned in the form of both acceleration of date of initiation of eltrombopag relative to the start of consolidation chemotherapy as well as increasing daily dosing. The Phase II portion will be conducted using the dose and schedule selected from the Phase I portion of the study for those patients in first complete remission. Patients will be used as their own controls, e.g., a two-period two-treatment cross-over design. Patients will be randomly allocated 1:1 to one of two sequences. Patients randomized to Sequence A will receive eltrombopag with their first cycle of consolidation and placebo with Cycle 2. Patients randomized to Sequence B will receive placebo with their first cycle of consolidation and eltrombopag with Cycle 2. The treatment assignment will be blinded to the patient and all study/sponsor personnel. Patients will undergo blood sample collection for Thrombopoietin(TPO)/ Erythropoietin(EPO) and pharmacokinetic analysis of eltrombopag in Phase I and pharmacokinetic analysis of eltrombopag in the Phase II portion of the study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 15
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Cytomorphologically documented diagnosis of acute myeloid leukemia (AML). Acute promyelocytic leukemia patients will be excluded (FAB M3). FAB classification, cytogenetics and molecular markers (if applicable) must be available at registration.

Phase I Enrollment:

• Must be in first or second complete remission, e.g., no evidence of active disease in blood, bone marrow (<5% blasts), or other tissues.
• For each remission, may have received no more than 2 cycles of induction treatment (any type).
• May have received no more than one course of consolidation for the current remission prior to enrollment (any type)

Phase II Enrollment:

• Must be in first complete remission, e.g., no evidence of active disease in blood, bone marrow (<5% blasts), or other tissues.
• May have received no more than 2 cycles of induction treatment (any type).

Enrollment in Either Phase:

• Remission status must be documented by a bone marrow examination up to 28 days prior to study registration.
• Have recovered from induction and first consolidation (if applicable) therapy side effects (or =grade 1).
• =18 years of age and =70 years of age.
• ECOG performance status 0, 1, 2.
• Have not received cytotoxic drug therapy within 21 days of registration.
• Have not received hematopoietic colony stimulating growth factors within 14 days of registration.
• Have not received packed red blood cells or platelets within 7 days of registration.
• Have not received investigational agents within 30 days of registration and will not receive any investigational agents other than eltrombopag/placebo during study.
• Signed IRB-approved informed consent.
• Willing to provide blood samples for research purposes.
• Adequate organ function obtained within 28 days prior to registration:
• Absolute neutrophil count >1 x 10?/L
• Platelet count >100 x 10?/L
• Total direct serum bilirubin =1.5x upper limit of normal (ULN)
• ALT and AST =3x ULN
• BUN and serum creatinine <2x ULN
• Albumin =2.5 g/dL
• PT and PTT 80-120% of institutional normal range
• Women of childbearing potential must have a negative serum pregnancy test within 14 days of registration.
• Not pregnant nor breast feeding.
• Women of childbearing potential and sexually active males must use an accepted and effective method of contraception.
• Patients of known East Asian ancestry (Chinese, Japanese, Taiwanese, and Korean) are excluded from protocol participation for safety and efficacy reasons.
• Able to swallow and retain orally administered medication.
• No clinically significant gastrointestinal abnormalities such as malabsorption syndrome or major resection of the stomach or bowels.
• No clinical evidence of hepatomegaly or splenomegaly.
• No known risk for Torsades de Pointes. (Eltrombopag use has not been shown to be associated with Torsades de Pointes.)
• No active or unresolved infection and must be off all antibiotics for at least 7 days prior to registration.
• No current evidence of invasive fungal infection.
• No known Hepatitis B, Hepatitis C active disease.
• No known Human Immunodeficiency Virus (HIV) seropositivity. The risk for potential toxicities secondary to HIV (e.g., increased risk for fatal opportunistic infection) may confound the toxicity profile of eltrombopag.
• Patients with a history of Central Nervous System (CNS) leukemia are eligible if there is documentation of no current CNS involvement on cerebrospinal fluid (CSF) examination (e.g., negative CSF by lumbar puncture) within 28 days of registration.
• No prior or concomitant malignancy in the past 5 years which is currently active and likely to interfere with the patient's treatment for AML or which is likely to increase the patient's morbidity or mortality. No prior chemotherapy or radiation therapy allowed (unless related to AML treatment).
• No concurrent organ damage or medical problems that would prohibit therapy.

Related Conditions & MeSH terms

• Acute Myeloid Leukemia
• Leukemia
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute

Intervention

Drug:
• Phase I- Cytarabine & Eltrombopag
Cycle 1= Cytarabine 3 g/m² IV twice daily on Days 1, 3 and 5 (Patients >60 years of age will receive cytarabine 1.5 g/m² IV per dose). Day 1 must start in AM. Eltrombopag (Open-Label) by mouth daily until platelet recovery or for 35 consecutive days, whichever occurs first. Phase I will determine the dose and schedule of Eltrombopag to be used in Phase II. One cycle of consolidation therapy with high-dose cytarabine and eltrombopag will be received on study. Additional chemotherapy may be administered at the investigators discretion without eltrombopag.
• Phase II- Sequence A
Cytarabine 3 g/m² IV twice daily on Days 1, 3 and 5 (Patients >60 years of age will receive cytarabine 1.5 g/m² IV per dose). Day 1 must start in AM. Eltrombopag by mouth daily (dose and schedule as determined in Phase I) with 1st cycle of high-dose consolidation chemotherapy and placebo by mouth daily with 2nd cycle. Eltrombopag/placebo will continue until platelet recovery or for 35 consecutive days, whichever occurs first. Additional chemotherapy may be administered at the investigators discretion without eltrombopag.
• Phase II- Sequence B
Cytarabine 3 g/m² IV twice daily on Days 1, 3 and 5 (Patients >60 years of age will receive cytarabine 1.5 g/m² IV per dose). Day 1 must start in AM. Placebo by mouth daily with 1st cycle of high-dose consolidation therapy and Eltrombopag by mouth daily (dose and schedule as determined in Phase I) with 2nd cycle. Eltrombopag/placebo will continue until platelet recovery or for 35 consecutive days, whichever occurs first. Additional chemotherapy may be administered at the investigators discretion without eltrombopag.

Locations

Country	Name	City	State
United States	University Hospitals Case Medical Center	Cleveland	Ohio
United States	Penn State Hershey Cancer Institute	Hershey	Pennsylvania
United States	Vanderbilt University	Nashville	Tennessee
United States	Mayo Clinic, Rochester	Rochester	Minnesota
United States	University of Massachusetts Worcester	Worcester	Massachusetts

Sponsors (3)

Lead Sponsor	Collaborator
PrECOG, LLC.	GlaxoSmithKline, Novartis

Country where clinical trial is conducted

United States, 

References & Publications (5)

Kellum A, Jagiello-Gruszfeld A, Bondarenko IN, Patwardhan R, Messam C, Mostafa Kamel Y. A randomized, double-blind, placebo-controlled, dose ranging study to assess the efficacy and safety of eltrombopag in patients receiving carboplatin/paclitaxel for advanced solid tumors. Curr Med Res Opin. 2010 Oct;26(10):2339-46. doi: 10.1185/03007995.2010.510051. — View Citation

Mavroudi I, Pyrovolaki K, Pavlaki K, Kozana A, Psyllaki M, Kalpadakis C, Pontikoglou C, Papadaki HA. Effect of the nonpeptide thrombopoietin receptor agonist eltrombopag on megakaryopoiesis of patients with lower risk myelodysplastic syndrome. Leuk Res. 2011 Mar;35(3):323-8. doi: 10.1016/j.leukres.2010.06.029. Epub 2010 Aug 4. — View Citation

Strickland SA, Wang XV, Cerny J, Rowe JM, Rybka W, Tallman MS, Litzow M, Lazarus HM. A novel PrECOG (PrE0901) dose-escalation trial using eltrombopag: enhanced platelet recovery during consolidation therapy in acute myeloid leukemia. Leuk Lymphoma. 2020 S — View Citation

Vadhan-Raj S. Management of chemotherapy-induced thrombocytopenia: current status of thrombopoietic agents. Semin Hematol. 2009 Jan;46(1 Suppl 2):S26-32. doi: 10.1053/j.seminhematol.2008.12.007. Review. — View Citation

Will B, Kawahara M, Luciano JP, Bruns I, Parekh S, Erickson-Miller CL, Aivado MA, Verma A, Steidl U. Effect of the nonpeptide thrombopoietin receptor agonist Eltrombopag on bone marrow cells from patients with acute myeloid leukemia and myelodysplastic syndrome. Blood. 2009 Oct 29;114(18):3899-908. doi: 10.1182/blood-2009-04-219493. Epub 2009 Aug 26. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Exploratory- Eltrombopag Effect on TPO/EPO	To determine if eltrombopag has an effect on TPO and/or EPO in this setting.	62 months
Primary	Phase I- Optimal Tolerated Dose of Eltrombopag	To determine the safety, tolerability and optimal dose of eltrombopag in acute myeloid leukemia patients in complete remission receiving intensive consolidation chemotherapy. The optimal dose was based on rules involving observation of Dose Limiting Toxicity (DLT events), defined as a CTCAE Version 4 non-hematologic adverse event of grade 3 or higher occurring within 30 days of the last dose of eltrombopag judged by the investigator to be at least possibly related to eltrombopag administration.	13 months
Primary	Phase I - Dose Level With Best Kinetics of Platelet Count Recovery	To describe the kinetics of platelet count recovery in acute myeloid leukemia patients in complete remission receiving intensive consolidation chemotherapy who will be receiving eltrombopag. This is assessed graphically by plotting platelet count vs. days relative to start of cytarabine for each patient.	13 months
Primary	Phase II- Assess if Platelet Count Recovery is Increased With Eltrombopag	To determine if platelet recovery following consolidation chemotherapy is accelerated with eltrombopag.	62 months
Secondary	Phase I & Phase II- Pharmacokinetics of Eltrombopag	To determine the plasma concentrations of eltrombopag in acute myeloid leukemia patients in complete remission receiving intensive consolidation chemotherapy (selected dosing regimen only).	62 months
Secondary	Phase II- Platelet Transfusion Requirements	To determine the impact of eltrombopag on platelet transfusion requirements in the setting of consolidation chemotherapy.	62 months
Secondary	Phase II- Red Blood Cell Transfusion Requirements	To determine the impact of eltrombopag on red blood cell transfusion requirements.	62 months
Secondary	Phase II- Bleeding Event Occurrence	To determine the impact of eltrombopag on occurrence of bleeding events.	62 months
Secondary	Phase II- Time to Platelet Count Recovery	To determine the impact of eltrombopag on time to platelet recovery following consolidation chemotherapy.	62 months
Secondary	Phase II- Depth of Platelet Nadir	To determine the impact of eltrombopag on the depth of platelet nadir following a cycle of consolidation chemotherapy.	62 months
Secondary	Phase II- Duration of Platelet Nadir	To determine the duration of platelet nadir in the setting of eltrombopag exposure.	62 months
Secondary	Phase II- Safety of Eltrombopag With Consolidation	To determine the safety and tolerability of eltrombopag when given at the optimal dose in the setting of consolidation chemotherapy.	62 months