Allogeneic Mesenchymal Cell Therapy in Anthracycline-Induced Cardiomyopathy Heart Failure Patients

医学 心力衰竭 间充质干细胞 心肌病 射血分数 内科学 临床终点 生活质量(医疗保健) 心脏病学 蒽环类 心功能曲线 肿瘤科 癌症 临床试验 乳腺癌 病理 护理部
作者
Roberto Bolli,Emerson C. Perin,James T. Willerson,Phillip Chung-Ming Yang,Jay H. Traverse,Timothy D. Henry,Carl J. Pepine,Raul David Mitrani,Joshua M. Hare,Michael P. Murphy,Keith L. March,Sohail Ikram,David P. Lee,Connor O’Brien,Jean‐Bernard Durand,Kathy D. Miller,João A.C. Lima,Mohammad Reza Ostovaneh,Bharath Ambale‐Venkatesh,Adrian P. Gee
出处
期刊:JACC: Cardiooncology [Elsevier BV]
卷期号:2 (4): 581-595 被引量:57
标识
DOI:10.1016/j.jaccao.2020.09.001
摘要

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: 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.
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