TY - JOUR
T1 - Effectiveness of sacubitril-valsartan in patients with cancer therapy-related cardiac dysfunction
T2 - a systematic review of clinical and preclinical studies
AU - Duraes, Andre R.
AU - de Souza Lima Bitar, Yasmin
AU - Neto, Mansueto G.
AU - Mesquita, Evandro T.
AU - Chan, Jeffrey S.
AU - Tse, Gary
AU - Liu, Tong
AU - Bocchi, Edimar A.
AU - Biondi-Zoccai, Giuseppe
AU - Roever, Leonardo
N1 - Publisher Copyright:
© 2022 EDIZIONI MINERVA MEDICA.
PY - 2022/6
Y1 - 2022/6
N2 - INTRODUCTION: Cancer therapy-related cardiac dysfunction (CTRCD) is a critical problem with an impact on both oncological and cardiovascular prognosis, especially when it prevents patients from receiving cancer treatment. However, there are very limited data on the efficacy of sacubitril/valsartan in the prevention and treatment of cardiotoxicity. This systematic review aimed to evaluate the potential benefit of sacubitril/valsartan in patients with CTRCD. EVIDENCE ACQUISITION: The databases included MEDLINE, Embase, LILACS, Scopus and Cochrane Central up to January 20, 2022. All pre-clinical and clinical studies including observational studies (cohorts, case-control, cross-sectional and case reports) that used sacubitril/valsartan for prevention or treatment of CTRCD. The primary effectiveness endpoints was CTRCD, defined as a clinically significant change in left ventricular ejection fraction (LVEF) at the end of the follow-up. EVIDENCE SYNTHESIS: And after applying the eligibility criteria, 12 articles (9 in humans and 3 preclinical studies) were included in this systematic review. The 3 preclinical studies demonstrated beneficial effects in preventing, attenuating and/or delaying the onset of myocardial damage at the cellular level, ventricular dysfunction and remodeling. Regardind human studies, most of them were composed of case reports. The largest study consisted of a retrospective multicentric cohort with 64 patients. CONCLUSIONS: All clinical studies have demonstrated that used Sac/Val in human showed a significant increase in LVEF, and when reported, a reduction in left ventricular volume and NT-proBNP (or BNP). Randomized clinical trials are needed to confirm this hypothesis.
AB - INTRODUCTION: Cancer therapy-related cardiac dysfunction (CTRCD) is a critical problem with an impact on both oncological and cardiovascular prognosis, especially when it prevents patients from receiving cancer treatment. However, there are very limited data on the efficacy of sacubitril/valsartan in the prevention and treatment of cardiotoxicity. This systematic review aimed to evaluate the potential benefit of sacubitril/valsartan in patients with CTRCD. EVIDENCE ACQUISITION: The databases included MEDLINE, Embase, LILACS, Scopus and Cochrane Central up to January 20, 2022. All pre-clinical and clinical studies including observational studies (cohorts, case-control, cross-sectional and case reports) that used sacubitril/valsartan for prevention or treatment of CTRCD. The primary effectiveness endpoints was CTRCD, defined as a clinically significant change in left ventricular ejection fraction (LVEF) at the end of the follow-up. EVIDENCE SYNTHESIS: And after applying the eligibility criteria, 12 articles (9 in humans and 3 preclinical studies) were included in this systematic review. The 3 preclinical studies demonstrated beneficial effects in preventing, attenuating and/or delaying the onset of myocardial damage at the cellular level, ventricular dysfunction and remodeling. Regardind human studies, most of them were composed of case reports. The largest study consisted of a retrospective multicentric cohort with 64 patients. CONCLUSIONS: All clinical studies have demonstrated that used Sac/Val in human showed a significant increase in LVEF, and when reported, a reduction in left ventricular volume and NT-proBNP (or BNP). Randomized clinical trials are needed to confirm this hypothesis.
KW - Cardiotoxicity
KW - Heart failure
KW - Neoplasms
KW - Sacubitril and valsartan sodium hydrate drug combination
UR - http://www.scopus.com/inward/record.url?scp=85134721072&partnerID=8YFLogxK
U2 - 10.23736/S0026-4806.22.08029-6
DO - 10.23736/S0026-4806.22.08029-6
M3 - Review article
C2 - 35156789
AN - SCOPUS:85134721072
SN - 0026-4806
VL - 113
SP - 551
EP - 557
JO - Minerva Medica
JF - Minerva Medica
IS - 3
ER -