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Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients: The CCTRN SENECA Trial

BACKGROUND: Anthracycline-induced cardiomyopathy (AIC) may be irreversible with a poor prognosis, disproportionately affecting women and young adults. Administration of allogeneic bone marrow–derived mesenchymal stromal cells (allo-MSCs) is a promising approach to heart failure (HF) treatment. OBJEC...

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Autores principales: Bolli, Roberto, Perin, Emerson C., Willerson, James T., Yang, Phillip C., Traverse, Jay H., Henry, Timothy D., Pepine, Carl J., Mitrani, Raul D., Hare, Joshua M., Murphy, Michael P., March, Keith L., Ikram, Sohail, Lee, David P., O’Brien, Connor, Durand, Jean-Bernard, Miller, Kathy, Lima, Joao A., Ostovaneh, Mohammad R., Ambale-Venkatesh, Bharath, Gee, Adrian P., Richman, Sara, Taylor, Doris A., Sayre, Shelly L., Bettencourt, Judy, Vojvodic, Rachel W., Cohen, Michelle L., Simpson, Lara M., Lai, Dejian, Aguilar, David, Loghin, Catalin, Moyé, Lem, Ebert, Ray F., Davis, Barry R., Simari, Robert D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781291/
https://www.ncbi.nlm.nih.gov/pubmed/33403362
http://dx.doi.org/10.1016/j.jaccao.2020.09.001
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author Bolli, Roberto
Perin, Emerson C.
Willerson, James T.
Yang, Phillip C.
Traverse, Jay H.
Henry, Timothy D.
Pepine, Carl J.
Mitrani, Raul D.
Hare, Joshua M.
Murphy, Michael P.
March, Keith L.
Ikram, Sohail
Lee, David P.
O’Brien, Connor
Durand, Jean-Bernard
Miller, Kathy
Lima, Joao A.
Ostovaneh, Mohammad R.
Ambale-Venkatesh, Bharath
Gee, Adrian P.
Richman, Sara
Taylor, Doris A.
Sayre, Shelly L.
Bettencourt, Judy
Vojvodic, Rachel W.
Cohen, Michelle L.
Simpson, Lara M.
Lai, Dejian
Aguilar, David
Loghin, Catalin
Moyé, Lem
Ebert, Ray F.
Davis, Barry R.
Simari, Robert D.
author_facet Bolli, Roberto
Perin, Emerson C.
Willerson, James T.
Yang, Phillip C.
Traverse, Jay H.
Henry, Timothy D.
Pepine, Carl J.
Mitrani, Raul D.
Hare, Joshua M.
Murphy, Michael P.
March, Keith L.
Ikram, Sohail
Lee, David P.
O’Brien, Connor
Durand, Jean-Bernard
Miller, Kathy
Lima, Joao A.
Ostovaneh, Mohammad R.
Ambale-Venkatesh, Bharath
Gee, Adrian P.
Richman, Sara
Taylor, Doris A.
Sayre, Shelly L.
Bettencourt, Judy
Vojvodic, Rachel W.
Cohen, Michelle L.
Simpson, Lara M.
Lai, Dejian
Aguilar, David
Loghin, Catalin
Moyé, Lem
Ebert, Ray F.
Davis, Barry R.
Simari, Robert D.
author_sort Bolli, Roberto
collection PubMed
description BACKGROUND: Anthracycline-induced cardiomyopathy (AIC) may be irreversible with a poor prognosis, disproportionately affecting women and young adults. Administration of allogeneic bone marrow–derived mesenchymal stromal cells (allo-MSCs) is a promising approach to heart failure (HF) treatment. OBJECTIVES: SENECA (Stem Cell Injection in Cancer Survivors) was a phase 1 study of allo-MSCs in AIC. METHODS: Cancer survivors with chronic AIC (mean age 56.6 years; 68% women; NT-proBNP 1,426 pg/ml; 6 enrolled in an open-label, lead-in phase and 31 subjects randomized 1:1) received 1 × 10(8) allo-MSCs or vehicle transendocardially. Primary objectives were safety and feasibility. Secondary efficacy measures included cardiac function and structure measured by cardiac magnetic resonance imaging (CMR), functional capacity, quality of life (Minnesota Living with Heart Failure Questionnaire), and biomarkers. RESULTS: A total of 97% of subjects underwent successful study product injections; all allo-MSC–assigned subjects received the target dose of cells. Follow-up visits were well-attended (92%) with successful collection of endpoints in 94% at the 1-year visit. Although 58% of subjects had non-CMR compatible devices, CMR endpoints were successfully collected in 84% of subjects imaged at 1 year. No new tumors were reported. There were no significant differences between allo-MSC and vehicle groups with regard to clinical outcomes. Secondary measures included 6-min walk test (p = 0.056) and Minnesota Living with Heart Failure Questionnaire score (p = 0.048), which tended to favor the allo-MSC group. CONCLUSIONS: In this first-in-human study of cell therapy in patients with AIC, transendocardial administration of allo-MSCs appears safe and feasible, and CMR was successfully performed in the majority of the HF patients with devices. This study lays the groundwork for phase 2 trials aimed at assessing efficacy of cell therapy in patients with AIC. (Stem Cell Injection in Cancer Survivors [SENECA]; NCT02509156)
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spelling pubmed-77812912021-01-04 Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients: The CCTRN SENECA Trial Bolli, Roberto Perin, Emerson C. Willerson, James T. Yang, Phillip C. Traverse, Jay H. Henry, Timothy D. Pepine, Carl J. Mitrani, Raul D. Hare, Joshua M. Murphy, Michael P. March, Keith L. Ikram, Sohail Lee, David P. O’Brien, Connor Durand, Jean-Bernard Miller, Kathy Lima, Joao A. Ostovaneh, Mohammad R. Ambale-Venkatesh, Bharath Gee, Adrian P. Richman, Sara Taylor, Doris A. Sayre, Shelly L. Bettencourt, Judy Vojvodic, Rachel W. Cohen, Michelle L. Simpson, Lara M. Lai, Dejian Aguilar, David Loghin, Catalin Moyé, Lem Ebert, Ray F. Davis, Barry R. Simari, Robert D. JACC CardioOncol Original Research BACKGROUND: Anthracycline-induced cardiomyopathy (AIC) may be irreversible with a poor prognosis, disproportionately affecting women and young adults. Administration of allogeneic bone marrow–derived mesenchymal stromal cells (allo-MSCs) is a promising approach to heart failure (HF) treatment. OBJECTIVES: SENECA (Stem Cell Injection in Cancer Survivors) was a phase 1 study of allo-MSCs in AIC. METHODS: Cancer survivors with chronic AIC (mean age 56.6 years; 68% women; NT-proBNP 1,426 pg/ml; 6 enrolled in an open-label, lead-in phase and 31 subjects randomized 1:1) received 1 × 10(8) allo-MSCs or vehicle transendocardially. Primary objectives were safety and feasibility. Secondary efficacy measures included cardiac function and structure measured by cardiac magnetic resonance imaging (CMR), functional capacity, quality of life (Minnesota Living with Heart Failure Questionnaire), and biomarkers. RESULTS: A total of 97% of subjects underwent successful study product injections; all allo-MSC–assigned subjects received the target dose of cells. Follow-up visits were well-attended (92%) with successful collection of endpoints in 94% at the 1-year visit. Although 58% of subjects had non-CMR compatible devices, CMR endpoints were successfully collected in 84% of subjects imaged at 1 year. No new tumors were reported. There were no significant differences between allo-MSC and vehicle groups with regard to clinical outcomes. Secondary measures included 6-min walk test (p = 0.056) and Minnesota Living with Heart Failure Questionnaire score (p = 0.048), which tended to favor the allo-MSC group. CONCLUSIONS: In this first-in-human study of cell therapy in patients with AIC, transendocardial administration of allo-MSCs appears safe and feasible, and CMR was successfully performed in the majority of the HF patients with devices. This study lays the groundwork for phase 2 trials aimed at assessing efficacy of cell therapy in patients with AIC. (Stem Cell Injection in Cancer Survivors [SENECA]; NCT02509156) Elsevier 2020-09-30 /pmc/articles/PMC7781291/ /pubmed/33403362 http://dx.doi.org/10.1016/j.jaccao.2020.09.001 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Bolli, Roberto
Perin, Emerson C.
Willerson, James T.
Yang, Phillip C.
Traverse, Jay H.
Henry, Timothy D.
Pepine, Carl J.
Mitrani, Raul D.
Hare, Joshua M.
Murphy, Michael P.
March, Keith L.
Ikram, Sohail
Lee, David P.
O’Brien, Connor
Durand, Jean-Bernard
Miller, Kathy
Lima, Joao A.
Ostovaneh, Mohammad R.
Ambale-Venkatesh, Bharath
Gee, Adrian P.
Richman, Sara
Taylor, Doris A.
Sayre, Shelly L.
Bettencourt, Judy
Vojvodic, Rachel W.
Cohen, Michelle L.
Simpson, Lara M.
Lai, Dejian
Aguilar, David
Loghin, Catalin
Moyé, Lem
Ebert, Ray F.
Davis, Barry R.
Simari, Robert D.
Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients: The CCTRN SENECA Trial
title Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients: The CCTRN SENECA Trial
title_full Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients: The CCTRN SENECA Trial
title_fullStr Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients: The CCTRN SENECA Trial
title_full_unstemmed Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients: The CCTRN SENECA Trial
title_short Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients: The CCTRN SENECA Trial
title_sort allogeneic mesenchymal cell therapy in anthracycline-induced cardiomyopathy heart failure patients: the cctrn seneca trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781291/
https://www.ncbi.nlm.nih.gov/pubmed/33403362
http://dx.doi.org/10.1016/j.jaccao.2020.09.001
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