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Prevention of Left Ventricular Dysfunction During Chemotherapy (OVERCOME)

Primary Purpose

Acute Myeloid Leukemia, Precursor-cell Lymphoblastic Leukemia-Lymphoma, Lymphoid Neoplasm

Status
Completed
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Enalapril and carvedilol
Sponsored by
Hospital Clinic of Barcelona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Acute Myeloid Leukemia focused on measuring Prevention, ventricular dysfunction, chemotherapy, acute myeloid leukemia, precursor-cell lymphoblastic leukemia, multiple myeloma, lymphoma, ejection fraction, Autologous hematopoietic stem cell transplantation

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients 18-70 years old
  • Sinus rhythm
  • Normal LVEF (>=50%)
  • Patients recently diagnosed of acute leukemia to be submitted to intensive chemotherapy or
  • Patients with other hemopathies submitted to autologous peripheral blood stem cell transplantation
  • Signed informed consent

Exclusion Criteria:

  • Congestive heart failure
  • LVEF<50%
  • Coronary artery disease,
  • significant valvulopathy or myocardiopathy
  • Renal failure (MDRD<30)
  • Liver failure
  • Ongoing or expected need to be treated with angiotensin-converting enzyme inhibitors (ACE-i),angiotensin II receptor blockers (ARB) or beta-blockers
  • Prior allergy to ACEI or ARB
  • Systolic blood pressure <90 mmHg
  • Asthma
  • Auriculoventricular (AV) block or sinus bradycardia (HR<60 bpm)
  • Persistent atrial fibrillation
  • Need to be treated with Class I antiarrhythmic drugs
  • Pregnancy
  • Inability or unwillingness to give unformed consent

Sites / Locations

  • Hospital Clinic
  • Hospital Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Enalapril and carvedilol

Control

Arm Description

Enalapril 2.5 to 10 mg BID plus Carvedilol 6.25 to 25 mg BID

Control arm without intervention

Outcomes

Primary Outcome Measures

Change from baseline in left ventricular ejection fraction (LVEF) measured by echocardiography and by cardiac magnetic resonance imaging (CMR).

Secondary Outcome Measures

Incidence of death, heart failure or LV systolic disfunction (LVEF<45%)
Assessment of genetic polymorphisms involved in chemotherapy-induced cardiotoxicity
Prognostic value for cardiac toxicity of troponin I and BNP
Right and left ventricular volumes measured by CMR
Subgroup analysis by diagnosis (acute leukemia vs. other malignant hemopathies submitted to autologous peripheral blood stem cell transplantation), and positive biomarkers (TnI, BNP).
Incidence of an absolute decrease in LVEF>10 percent units associated with a decline below its normal limit of 50%
Serious adverse events
the incidence of LV dysfunction as assessed by the measurement of the LV strain, and of diastolic dysfunction measured by echo-Doppler

Full Information

First Posted
April 23, 2010
Last Updated
November 14, 2013
Sponsor
Hospital Clinic of Barcelona
Collaborators
Instituto de Salud Carlos III, European Union
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1. Study Identification

Unique Protocol Identification Number
NCT01110824
Brief Title
Prevention of Left Ventricular Dysfunction During Chemotherapy
Acronym
OVERCOME
Official Title
Prevention of Left Ventricular Dysfunction With Enalapril and Carvedilol in Patients Submitted to Intensive Chemotherapy for the Treatment of Malignant Hemopathies
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Clinic of Barcelona
Collaborators
Instituto de Salud Carlos III, European Union

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators' objective is to assess the efficacy of the combined treatment with enalapril and carvedilol in the prevention of left ventricular systolic dysfunction in patients with hematological malignancies submitted to intensive chemotherapy with potential cardiotoxicity. The hypothesis is that these drugs administered during chemotherapy may prevent left ventricular systolic dysfunction.
Detailed Description
The prognosis of patients with hematological malignancies has greatly improved in the last years with the use of new chemotherapeutic drugs and regimens at the cost of significant adverse events such as cardiac toxicity. Asymptomatic left ventricular systolic dysfunction limits the specific treatment of the patients and their long-term survival, since a significant proportion of them will relapse within 5 years after front-line therapy and will require further salvage treatment, including hematopoietic stem-cell transplantation in most instances. Angiotensin-converting enzyme inhibitors (ACEIs) have showed to have preventive effects against chemotherapy-induced cardiotoxicity in animal models, and in patients with early cardiotoxicity. Carvedilol prevent free radical release, mitochondrial dysfunction, apoptosis, and dilated cardiomyopathy in animals treated with anthracyclines, and have shown promising results in preventing chemotherapy-induced left ventricular dysfunction in patients. As demonstrated in post-infarction patients, the combined treatment with an ACEI and carvedilol could have additive effects to prevent LV dysfunction in patients with hematological malignancies at high risk of cardiac toxicity. Therefore, we designed the OVERCOME (preventiOn of left Ventricular dysfunction with Enalapril and caRvedilol in patients submitted to intensive ChemOtherapy for the treatment of Malignant hEmopathies) study, a prospective, randomized trial to evaluate the combined effect of enalapril and carvedilol on the prevention of left ventricular dysfunction in patients with malignant hemopathies undergoing intensive chemotherapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia, Precursor-cell Lymphoblastic Leukemia-Lymphoma, Lymphoid Neoplasm, Multiple Myeloma, Lymphoma, Autologous Hematopoietic Stem Cell Transplantation
Keywords
Prevention, ventricular dysfunction, chemotherapy, acute myeloid leukemia, precursor-cell lymphoblastic leukemia, multiple myeloma, lymphoma, ejection fraction, Autologous hematopoietic stem cell transplantation

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enalapril and carvedilol
Arm Type
Experimental
Arm Description
Enalapril 2.5 to 10 mg BID plus Carvedilol 6.25 to 25 mg BID
Arm Title
Control
Arm Type
No Intervention
Arm Description
Control arm without intervention
Intervention Type
Drug
Intervention Name(s)
Enalapril and carvedilol
Intervention Description
Enalapril 2.5 to 10 mg BID Carvedilol 6.25 to 25 mg BID
Primary Outcome Measure Information:
Title
Change from baseline in left ventricular ejection fraction (LVEF) measured by echocardiography and by cardiac magnetic resonance imaging (CMR).
Time Frame
6 months after randomization
Secondary Outcome Measure Information:
Title
Incidence of death, heart failure or LV systolic disfunction (LVEF<45%)
Time Frame
6 months after randomization
Title
Assessment of genetic polymorphisms involved in chemotherapy-induced cardiotoxicity
Time Frame
Baseline
Title
Prognostic value for cardiac toxicity of troponin I and BNP
Time Frame
up to 3 months
Title
Right and left ventricular volumes measured by CMR
Time Frame
6 months after randomization
Title
Subgroup analysis by diagnosis (acute leukemia vs. other malignant hemopathies submitted to autologous peripheral blood stem cell transplantation), and positive biomarkers (TnI, BNP).
Time Frame
6 months after randomization
Title
Incidence of an absolute decrease in LVEF>10 percent units associated with a decline below its normal limit of 50%
Time Frame
6 months after randomization
Title
Serious adverse events
Time Frame
6 months after randomization
Title
the incidence of LV dysfunction as assessed by the measurement of the LV strain, and of diastolic dysfunction measured by echo-Doppler
Time Frame
6 months after randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients 18-70 years old Sinus rhythm Normal LVEF (>=50%) Patients recently diagnosed of acute leukemia to be submitted to intensive chemotherapy or Patients with other hemopathies submitted to autologous peripheral blood stem cell transplantation Signed informed consent Exclusion Criteria: Congestive heart failure LVEF<50% Coronary artery disease, significant valvulopathy or myocardiopathy Renal failure (MDRD<30) Liver failure Ongoing or expected need to be treated with angiotensin-converting enzyme inhibitors (ACE-i),angiotensin II receptor blockers (ARB) or beta-blockers Prior allergy to ACEI or ARB Systolic blood pressure <90 mmHg Asthma Auriculoventricular (AV) block or sinus bradycardia (HR<60 bpm) Persistent atrial fibrillation Need to be treated with Class I antiarrhythmic drugs Pregnancy Inability or unwillingness to give unformed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xavier Bosch, M.D., PhD.
Organizational Affiliation
Hospital Clinic, University of Barcelona
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital Clinic
City
Barcelona
State/Province
Catalunya
ZIP/Postal Code
08035
Country
Spain
Facility Name
Hospital Clinic
City
Barcelona
State/Province
Catalunya
ZIP/Postal Code
08036
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
21807325
Citation
Bosch X, Esteve J, Sitges M, de Caralt TM, Domenech A, Ortiz JT, Monzo M, Morales-Ruiz M, Perea RJ, Rovira M. Prevention of chemotherapy-induced left ventricular dysfunction with enalapril and carvedilol: rationale and design of the OVERCOME trial. J Card Fail. 2011 Aug;17(8):643-8. doi: 10.1016/j.cardfail.2011.03.008. Epub 2011 May 6.
Results Reference
background
PubMed Identifier
23583763
Citation
Bosch X, Rovira M, Sitges M, Domenech A, Ortiz-Perez JT, de Caralt TM, Morales-Ruiz M, Perea RJ, Monzo M, Esteve J. Enalapril and carvedilol for preventing chemotherapy-induced left ventricular systolic dysfunction in patients with malignant hemopathies: the OVERCOME trial (preventiOn of left Ventricular dysfunction with Enalapril and caRvedilol in patients submitted to intensive ChemOtherapy for the treatment of Malignant hEmopathies). J Am Coll Cardiol. 2013 Jun 11;61(23):2355-62. doi: 10.1016/j.jacc.2013.02.072. Epub 2013 Apr 10.
Results Reference
result

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Prevention of Left Ventricular Dysfunction During Chemotherapy

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