Mesenchymal Stromal Cells for Treating Steroid-Resistant Acute and Chronic Graft Versus Host Disease: A Multicenter Compassionate Use Experience

Author:

Macías-Sánchez María del Mar12ORCID,Morata-Tarifa Cynthia1,Cuende Natividad3,Cardesa-Gil Ana1,Cuesta-Casas María Ángeles4,Pascual-Cascon María Jesús4,Pascual Antonia4,Martín-Calvo Carmen5,Jurado Manuel6,Perez-Simón José Antonio78,Espigado Ildefonso78910,Garzón López Sebastián11,Carmona Sánchez Gloria1,Mata-Alcázar-Caballero Rosario1,Sánchez-Pernaute Rosario1ORCID

Affiliation:

1. Red Andaluza de Diseño y Traslación de Terapias Avanzadas, Fundación Pública Andaluza Progreso y Salud, Junta de Andalucía, Spain

2. Facultad de Medicina, Universidad de Málaga, Málaga, Spain

3. Coordinación Autonómica de Trasplantes de Andalucía. Servicio Andaluz de Salud, Sevilla, Spain

4. Departamento de Hematología y Hemoterapia, Hospital Regional Universitario de Málaga, Málaga, Spain

5. Departamento de Hematología, Hospital Universitario Reina Sofía, Córdoba, Spain

6. Departamento de Hematología, Hospital Virgen de las Nieves, Granada, Spain

7. Departamento de Hematología, Hospital Universitario Virgen del Rocío, Sevilla, Spain

8. Instituto de Investigación Biomédica de Sevilla (IBIS)/CSIC, Sevilla, Spain

9. Universidad de Sevilla, Sevilla, Spain

10. Hospital Universitario Virgen Macarena, Sevilla, Spain

11. Departamento de Hematología, Hospital Universitario de Jerez, Cádiz, Spain

Abstract

Abstract Graft versus host disease (GVHD) is a severe complication after allogenic hematopoietic cell transplantation (HSCT). Several clinical trials have reported the use of mesenchymal stromal cells (MSCs) for the treatment of GVHD. In March 2008, the Andalusian Health Care System launched a compassionate use program to treat steroid-resistant GVHD with MSC. Clinical-grade MSC were obtained under GMP conditions. MSC therapy was administered intravenously in four separate doses of 1 × 106 cells/kg. Sixty-two patients, 45 males (7 children) and 17 females (2 children), received the treatment. Patients had a median age of 39 years (range: 7–66) at the time of the allogenic HSCT. The overall response was achieved in 58.7% of patients with acute (a)GVHD. Two years’ survival for aGVHD responders was 51.85%. The overall response for patients with chronic (c)GVHD was 65.50% and the 2-year survival rate for responders was 70%. Age at the time of HSCT was the only predictor found to be inversely correlated with survival in aGVHD. Regarding safety, four adverse events were reported, all recovered without sequelae. Thus, analysis of this compassionate use experience shows MSC to be an effective and safe therapeutic option for treating refractory GVHD, resulting in a significant proportion of patients responding to the therapy.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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