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Autologous CD34+ cell therapy improves exercise capacity, angina frequency and reduces mortality in no-option
Timothy D Henry1, Douglas W Losordo2, Jay H Traverse3
1Cedars-Sinai Heart Institute, Los Angeles, CA, USA.
Insights
Autologous CD34+ cell therapy offers a promising treatment for refractory angina, significantly improving exercise tolerance and reducing angina frequency. This therapy also demonstrated a notable reduction in 24-month mortality in a patient-level meta-analysis.
Area of Science:
- Cardiovascular Medicine
- Regenerative Medicine
- Cell Therapy
Background:
- Refractory angina remains a therapeutic challenge, necessitating novel treatment strategies.
- Autologous CD34+ cells are being investigated for their potential to improve myocardial function and reduce symptoms in patients with ischemic heart disease.
Purpose of the Study:
- To evaluate the efficacy and safety of intramyocardial autologous CD34+ cell therapy in patients with refractory angina.
- To assess the impact of this therapy on total exercise time (TET), angina frequency (AF), and major adverse cardiac events (MACE).
Main Methods:
- A patient-level meta-analysis pooled data from three double-blinded randomized trials involving 304 patients.
- Intramyocardial autologous CD34+ cells were compared against placebo injections.
- Efficacy was assessed by analyzing changes in TET and AF, and the incidence of MACE.
Main Results:
- Autologous CD34+ cell therapy significantly improved TET at 3, 6, and 12 months.
- A significant reduction in angina frequency was observed at 3, 6, and 12 months post-treatment.
- The therapy led to a significant decrease in 24-month mortality (12.1% vs. 2.5%) and a numerical reduction in MACE.
Conclusions:
- Autologous CD34+ cell therapy provides clinically meaningful and durable improvements in exercise capacity and angina symptoms.
- The observed reduction in mortality highlights the potential long-term benefits of this regenerative approach for refractory angina.
Aims:
Autologous CD34+ (auto-CD34+) cells represent an attractive option for the treatment of refractory angina. Three double-blinded randomized trials (n = 304) compared intramyocardial (IM) auto-CD34+ cells with IM placebo injections to affect total exercise time (TET), angina frequency (AF), and major adverse cardiac events (MACE). Patient-level data were pooled from the Phase I, Phase II ACT-34, ACT-34 extension, and Phase III RENEW trials to determine the efficacy and safety of auto-CD34+ cells.
Methods And Results:
Treatment effects for TET were analysed using an analysis of covariance mixed-effects model and for AF using Poisson regression in a log linear model with repeated measures. The Kaplan-Meier rate estimates for MACE were compared using the log-rank test. Autologous CD34+ cell therapy improved TET by 46.6 s [3 months, 95% confidence interval (CI) 13.0 s-80.3 s; P = 0.007], 49.5 s (6 months, 95% CI 9.3-89.7; P = 0.016), and 44.7 s (12 months, 95% CI - 2.7 s-92.1 s; P = 0.065). The relative frequency of angina was 0.78 (95% CI 0.63-0.98; P = 0.032), 0.66 (0.48-0.91; P = 0.012), and 0.58 (0.38-0.88; P = 0.011) at 3-, 6- and 12-months in auto-CD34+ compared with placebo patients. Results remained concordant when analysed by treatment received and when confined to the Phase III dose of 1 × 105 cells/kg. Autologous CD34 + cell therapy significantly decreased mortality (12.1% vs. 2.5%; P = 0.0025) and numerically reduced MACE (38.9% vs. 30.0; P = 0.14) at 24 months.
Conclusion:
Treatment with auto-CD34+ cells resulted in clinically meaningful durable improvements in TET and AF at 3-, 6- and 12-months, as well as a reduction in 24-month mortality in this patient-level meta-analysis.
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