Abstract

This study sought to evaluate the efficacy of enalapril and carvedilol to prevent chemotherapy-induced left ventricular systolic dysfunction (LVSD) in patients with hematological malignancies. Current chemotherapy may induce LVSD. Angiotensin-converting enzyme inhibitors and beta-blockers prevent LVSD in animal models of anthracycline-induced cardiomyopathy. In this randomized, controlled study, 90 patients with recently diagnosed acute leukemia (n = 36) or patients with malignant hemopathies undergoing autologous hematopoietic stem cell transplantation (HSCT) (n = 54) and without LVSD were randomly assigned to a group receiving enalapril and carvedilol (n = 45) or to a control group (n = 45). Echocardiographic and cardiac magnetic resonance (CMR) imaging studies were performed before and at 6 months after randomization. The primary efficacy endpoint was the absolute change from baseline in LV ejection fraction (LVEF). The mean age of patients was 50 ± 13 years old, and 43% were women. At 6 months, LVEF did not change in the intervention group but significantly decreased in controls, resulting in a -3.1% absolute difference by echocardiography (p = 0.035) and -3.4% (p = 0.09) in the 59 patients who underwent CMR. The corresponding absolute difference (95% confidence interval [CI]) in LVEF was -6.38% (95% CI: -11.9 to -0.9) in patients with acute leukemia and -1.0% (95% CI: -4.5 to 2.5) in patients undergoing autologous HSCT (p = 0.08 for interaction between treatment effect and disease category). Compared to controls, patients in the intervention group had a lower incidence of the combined event of death or heart failure (6.7% vs. 22%, p = 0.036) and of death, heart failure, or a final LVEF <45% (6.7% vs. 24.4%, p = 0.02). Combined treatment with enalapril and carvedilol may prevent LVSD in patients with malignant hemopathies treated with intensive chemotherapy. The clinical relevance of this strategy should be confirmed in larger studies. (Prevention of Left Ventricular Dysfunction During Chemotherapy [OVERCOME]; NCT01110824).

Highlights

  • Высокая эффективность современной химиолучевой терапии позволила добиться больших успехов в лечении онкогематологических заболеваний

  • High efficacy of contemporary chemical and radiation treatments made it to success in treatment of oncohematological diseases

  • Effective treatment of the main disease in many cases is followed by a variety of cardiovascular complications, including severe ones and fatal

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Summary

Представители группы Область применения в онкологии

Кардиотоксические эффекты даунорубицин доксорубицин (адриамицин) эпирубицин (фарморубицин) идарубицин (заведос) митоксантрон. В сочетании с антрациклинами возможно развитие КМП с клинической картиной ХСН. Злокачественные новообразования миндалины; ротоглотки; носоглотки; желудка; тонкой кишки; прямой кишки; полости носа и среднего уха; придаточных пазух; гортани; бронхов и легкого; костей и суставных хрящей других и неуточненных локализаций (остеосаркома, рак остеогенный); мезотелиальных и мягких тканей; молочной железы; шейки и тела матки; яичника; плаценты; полового члена; предстательной железы; яичка; почечных лоханок; мочевого пузыря; головного мозга; надпочечника. При проведении высокодозовой химиотерапии возможно снижение амплитуды QRSкомплекса, неспецифические изменения зубца Т на ЭКГ, тахиаритмии. Сокращения: ФИ — фракция изгнания, КМП — кардиомиопатия, ЛЖ — левый желудочек, ХСН — хроническая сердечная недостаточность, ЭКГ — электрокардиография. Воздействие антрациклина на Top2b является ключевым фактором развития кар-

Саркома Лимфомы Лейкозы детей
Принципы профилактики АКМП
а дексразоксан
Findings
Кардиологическая симптоматика с или без снижения ФИ

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