TY - JOUR
T1 - Effect of allogeneic adipose tissue-derived mesenchymal stromal cell treatment in chronic ischaemic heart failure with reduced ejection fraction – the SCIENCE trial
AU - Qayyum, Abbas Ali
AU - van Klarenbosch, Bas
AU - Frljak, Sabina
AU - Cerar, Andraz
AU - Poglajen, Gregor
AU - Traxler-Weidenauer, Denise
AU - Nadrowski, Pawel
AU - Paitazoglou, Christina
AU - Vrtovec, Bojan
AU - Bergmann, Martin W.
AU - Chamuleau, Steven A.J.
AU - Wojakowski, Wojtek
AU - Gyöngyösi, Mariann
AU - Kraaijeveld, Adriaan
AU - Hansen, Kristian Schultz
AU - Vrangbæk, Karsten
AU - Jørgensen, Erik
AU - Helqvist, Steffen
AU - Joshi, Francis Richard
AU - Johansen, Ellen Mønsted
AU - Follin, Bjarke
AU - Juhl, Morten
AU - Højgaard, Lisbeth Drozd
AU - Mathiasen, Anders Bruun
AU - Ekblond, Annette
AU - Haack-Sørensen, Mandana
AU - Kastrup, Jens
N1 - Publisher Copyright:
© 2023 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
PY - 2023/4
Y1 - 2023/4
N2 - Aims: The aim of the SCIENCE trial was to investigate whether a single treatment with direct intramyocardial injections of adipose tissue-derived mesenchymal stromal cells (CSCC_ASCs) was safe and improved cardiac function in patients with chronic ischaemic heart failure with reduced ejection fraction (HFrEF). Methods and results: The study was a European multicentre, double-blind, placebo-controlled phase II trial using allogeneic CSCC_ASCs from healthy donors or placebo (2:1 randomization). Main inclusion criteria were New York Heart Association (NYHA) class II–III, left ventricular ejection fraction (LVEF) <45%, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels >300 pg/ml. CSCC_ASCs or placebo (isotonic saline) were injected directly into viable myocardium. The primary endpoint was change in left ventricular end-systolic volume (LVESV) at 6-month follow-up measured by echocardiography. A total of 133 symptomatic HFrEF patients were included. The treatment was safe without any drug-related severe adverse events or difference in cardiac-related adverse events during a 3-year follow-up period. There were no significant differences between groups during follow-up in LVESV (0.3 ± 5.0 ml, p = 0.945), nor in secondary endpoints of left ventricular end-diastolic volume (−2.0 ± 6.0 ml, p = 0.736) and LVEF (−1.6 ± 1.0%, p = 0.119). The NYHA class improved slightly within the first year in both groups without any difference between groups. There were no changes in 6-min walk test, NT-proBNP, C-reactive protein or quality of life the first year in any groups. Conclusion: The SCIENCE trial demonstrated safety of intramyocardial allogeneic CSCC_ASC therapy in patients with chronic HFrEF. However, it was not possible to improve the pre-defined endpoints and induce restoration of cardiac function or clinical symptoms.
AB - Aims: The aim of the SCIENCE trial was to investigate whether a single treatment with direct intramyocardial injections of adipose tissue-derived mesenchymal stromal cells (CSCC_ASCs) was safe and improved cardiac function in patients with chronic ischaemic heart failure with reduced ejection fraction (HFrEF). Methods and results: The study was a European multicentre, double-blind, placebo-controlled phase II trial using allogeneic CSCC_ASCs from healthy donors or placebo (2:1 randomization). Main inclusion criteria were New York Heart Association (NYHA) class II–III, left ventricular ejection fraction (LVEF) <45%, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels >300 pg/ml. CSCC_ASCs or placebo (isotonic saline) were injected directly into viable myocardium. The primary endpoint was change in left ventricular end-systolic volume (LVESV) at 6-month follow-up measured by echocardiography. A total of 133 symptomatic HFrEF patients were included. The treatment was safe without any drug-related severe adverse events or difference in cardiac-related adverse events during a 3-year follow-up period. There were no significant differences between groups during follow-up in LVESV (0.3 ± 5.0 ml, p = 0.945), nor in secondary endpoints of left ventricular end-diastolic volume (−2.0 ± 6.0 ml, p = 0.736) and LVEF (−1.6 ± 1.0%, p = 0.119). The NYHA class improved slightly within the first year in both groups without any difference between groups. There were no changes in 6-min walk test, NT-proBNP, C-reactive protein or quality of life the first year in any groups. Conclusion: The SCIENCE trial demonstrated safety of intramyocardial allogeneic CSCC_ASC therapy in patients with chronic HFrEF. However, it was not possible to improve the pre-defined endpoints and induce restoration of cardiac function or clinical symptoms.
KW - Adipose tissue derived-mesenchymal stromal cells
KW - Allogeneic therapy
KW - Clinical trial
KW - Heart failure
KW - Ischaemic cardiomyopathy
KW - Stem cells
UR - http://www.scopus.com/inward/record.url?scp=85147353159&partnerID=8YFLogxK
U2 - 10.1002/ejhf.2772
DO - 10.1002/ejhf.2772
M3 - Article
C2 - 36644821
AN - SCOPUS:85147353159
SN - 1388-9842
VL - 25
SP - 576
EP - 587
JO - European Journal of Heart Failure
JF - European Journal of Heart Failure
IS - 4
ER -