Protective effect of carvedilol on adriamycin-induced left ventricular dysfunction in children with acute lymphoblastic leukemia

J Card Fail. 2012 Aug;18(8):607-13. doi: 10.1016/j.cardfail.2012.06.416.

Abstract

Background: Adriamycin (ADR) is a potent chemotherapeutic agent widely used in the treatment of childhood acute lymphoblastic leukemia (ALL); its clinical use is limited owing to its marked cardiotoxicity. The present study investigated the possible protective role of carvedilol on ADR-induced left ventricular dysfunction in children with ALL.

Methods and results: Fifty children with newly diagnosed ALL were included in this study. They were divided into 2 equal groups: 1) ADR; and 2) ADR + carvedilol. Patients were evaluated with conventional 2-dimensional echocardiographic examination (2D), pulsed tissue Doppler (PTD), and 2-dimensional longitudinal strain echocardiography (2DS) before and after therapy. Plasma lactic dehydrogenase (LDH), creatine phosphokinase (CPK), and troponin I levels were also determined before and after therapy. ADR treatment reduced left ventricular systolic dysfunction as assessed by a significant decrease in fractional shortening (FS) (2D) and global peak-systolic strain (GPSS; 2DS). In addition, ADR treatment significantly increased plasma troponin I and LDH. Pretreatment of ADR-treated patients with carvedilol resulted in a significant increase in FS (2D) and GPSS (2DS). Furthermore, carvedilol pretreatment inhibited ADR-induced increase in plasma troponin I and LDH.

Conclusions: These results suggested a protective role of carvedilol against ADR-induced cardiotoxicity.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Antibiotics, Antineoplastic / adverse effects*
  • Carbazoles / pharmacology
  • Carbazoles / therapeutic use*
  • Carvedilol
  • Child
  • Child Welfare
  • Doxorubicin / adverse effects*
  • Female
  • Humans
  • Male
  • Pediatrics
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology*
  • Propanolamines / pharmacology
  • Propanolamines / therapeutic use*
  • Time Factors
  • Ultrasonography
  • Vasodilator Agents / pharmacology
  • Vasodilator Agents / therapeutic use*
  • Ventricular Dysfunction, Left / chemically induced*
  • Ventricular Dysfunction, Left / diagnostic imaging
  • Ventricular Dysfunction, Left / pathology

Substances

  • Antibiotics, Antineoplastic
  • Carbazoles
  • Propanolamines
  • Vasodilator Agents
  • Carvedilol
  • Doxorubicin