Long-Term and Sustained Therapeutic Results of a Specific Promonocyte Cell Formulation in Refractory Angina: ReACT® (Refractory Angina Cell Therapy) Clinical Update and Cost-Effective Analysis

Author:

Nelson Americo Hossne1,Cruz Eduardo23,Buffolo Enio1,De Siqueira Mac Dowell Coimbra Anna Carolina Teixeira23,Machado Janaina2,Goldenberg Regina Coeli Dos Santos4,Regazzi Germana23,Azevedo Silvia2,Invitti Adriana Luckow23,Branco João Nelson Rodrigues1,De Oliveira José Salvador Rodrigues5,Stolf Noedir Antonio Groppo6,Miller Leslie W.7,Sanberg Paul R.89

Affiliation:

1. Cardiovascular Surgery Division, Surgery Department, Paulista School of Medicine, Federal University of São Paulo, São Paulo, SP, Brazil

2. Cryopraxis Criobiologia Ltda, Polo de Biotecnologia do Rio de Janeiro — Cidade Universitária, Rio de Janeiro, RJ, Brazil

3. Cellpraxis Bioengeneering, Polo de Biotecnologia do Rio de Janeiro — Cidade Universitária, Rio de Janeiro, RJ, Brazil

4. Physiology Department, Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil

5. Hematology Division, Paulista School of Medicine, Federal University of São Paulo, São Paulo, SP, Brazil

6. Heart Institute, College of Medicine, University of São Paulo, São Paulo, SP, Brazil

7. Cardiology Department, University of South Florida, Tampa, FL, USA

8. Center of Excellence for Aging and Brain Repair, Department of Neurosurgery and Brain Repair, University of South Florida Morsani College of Medicine, Tampa, FL, USA

9. Office of Research and Innovation, University of South Florida, Tampa, FL, USA

Abstract

Mononuclear stem cells have been studied for their potential in myocardial ischemia. In our previous published article, ReACT® phase I/II clinical trial, our results suggest that a certain cell population, promonocytes, directly correlated with the perceived angiogenesis in refractory angina patients. This study is ReACT's clinical update, assessing long-term sustained efficacy. The ReACT phase IIA/B noncontrolled, open-label, clinical trial enrolled 14 patients with refractory angina and viable ischemic myocardium, without ventricular dysfunction, who were not suitable for myocardial revascularization. The procedure consisted of direct myocardial injection of a specific mononuclear cell formulation, with a certain percentage of promonocytes, in a single series of multiple injections (24—90; 0.2 ml each) into specific areas of the left ventricle. Primary endpoints were Canadian Cardiovascular Society Angina Classification (CCSAC) improvement at the 12-month follow-up and ischemic area reduction (scintigraphic analysis) at the 12-month follow-up, in correlation with ReACT's formulation. A recovery index (for patients with more than 1 year follow-up) was created to evaluate CCSAC over time, until April 2011. Almost all patients presented progressive improvement in CCSAC beginning 3 months ( p = 0.002) postprocedure, which was sustained at the 12-month follow-up ( p = 0.002), as well as objective myocardium ischemic area reduction at 6 months (decrease of 15%, p < 0.024) and 12 months (decrease of 100%, p < 0.004) The recovery index ( n = 10) showed that the patients were graded less than CCSAC 4 for 73.9 ± 24.2% over a median follow-up time of 46.8 months. After characterization, ReACT's promonocyte concentration suggested a positive correlation with CCSAC improvement ( r = −0.575, p = 0.082). Quality of life (SF-36 questionnaire) improved significantly in almost all domains. Cost-effectiveness analysis showed decrease in angina-related direct costs. Refractory angina patients presented a sustained long-term improvement in CCSAC and myocardium ischemic areas after the procedure. The long-term follow-up and strong improvement in quality of life reinforce effectiveness. Promonocytes may play a key role in myocardial neoangiogenesis. ReACT dramatically decreased direct costs.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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