Real-world data suggest effectiveness of the allogeneic mesenchymal stromal cells preparation MSC-FFM in ruxolitinib-refractory acute graft-versus-host disease.


Journal

Journal of translational medicine
ISSN: 1479-5876
Titre abrégé: J Transl Med
Pays: England
ID NLM: 101190741

Informations de publication

Date de publication:
21 Nov 2023
Historique:
received: 07 09 2023
accepted: 13 11 2023
medline: 23 11 2023
pubmed: 22 11 2023
entrez: 22 11 2023
Statut: epublish

Résumé

Patients with steroid-refractory acute graft-versus-host disease (aGvHD) not tolerating/responding to ruxolitinib (RR-aGvHD) have a dismal prognosis. We retrospectively assessed real-world outcomes of RR-aGvHD treated with the random-donor allogeneic MSC preparation MSC-FFM, available via Hospital Exemption in Germany. MSC-FFM is provided as frozen cell dispersion for administration as i.v. infusion immediately after thawing, at a recommended dose of 1-2 million MSCs/kg body weight in 4 once-weekly doses. 156 patients, 33 thereof children, received MSC-FFM; 5% had Grade II, 40% had Grade III, and 54% had Grade IV aGvHD. Median (range) number of prior therapies was 4 (1-10) in adults and 7 (2-11) in children. The safety profile of MSC-FFM was consistent with previous reports for MSC therapies in general and MSC-FFM specifically. The overall response rate at Day 28 was 46% (95% confidence interval [CI] 36-55%) in adults and 64% (45-80%) in children; most responses were durable. Probability of overall survival at 6, 12 and 24 months was 47% (38-56%), 35% (27-44%) and 30% (22-39%) for adults, and 59% (40-74%), 42% (24-58%) and 35% (19-53%) for children, respectively (whole cohort: median OS 5.8 months). A recent real-world analysis of outcomes for 64 adult RR-aGvHD patients not treated with MSCs reports survival of 20%, 16% and 10% beyond 6, 12 and 24 months, respectively (median 28 days). Our data thus suggest effectiveness of MSC-FFM in RR-aGvHD.

Sections du résumé

BACKGROUND BACKGROUND
Patients with steroid-refractory acute graft-versus-host disease (aGvHD) not tolerating/responding to ruxolitinib (RR-aGvHD) have a dismal prognosis.
METHODS METHODS
We retrospectively assessed real-world outcomes of RR-aGvHD treated with the random-donor allogeneic MSC preparation MSC-FFM, available via Hospital Exemption in Germany. MSC-FFM is provided as frozen cell dispersion for administration as i.v. infusion immediately after thawing, at a recommended dose of 1-2 million MSCs/kg body weight in 4 once-weekly doses. 156 patients, 33 thereof children, received MSC-FFM; 5% had Grade II, 40% had Grade III, and 54% had Grade IV aGvHD. Median (range) number of prior therapies was 4 (1-10) in adults and 7 (2-11) in children.
RESULTS RESULTS
The safety profile of MSC-FFM was consistent with previous reports for MSC therapies in general and MSC-FFM specifically. The overall response rate at Day 28 was 46% (95% confidence interval [CI] 36-55%) in adults and 64% (45-80%) in children; most responses were durable. Probability of overall survival at 6, 12 and 24 months was 47% (38-56%), 35% (27-44%) and 30% (22-39%) for adults, and 59% (40-74%), 42% (24-58%) and 35% (19-53%) for children, respectively (whole cohort: median OS 5.8 months).
CONCLUSION CONCLUSIONS
A recent real-world analysis of outcomes for 64 adult RR-aGvHD patients not treated with MSCs reports survival of 20%, 16% and 10% beyond 6, 12 and 24 months, respectively (median 28 days). Our data thus suggest effectiveness of MSC-FFM in RR-aGvHD.

Identifiants

pubmed: 37990219
doi: 10.1186/s12967-023-04731-1
pii: 10.1186/s12967-023-04731-1
pmc: PMC10664468
doi:

Substances chimiques

ruxolitinib 82S8X8XX8H

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

837

Informations de copyright

© 2023. The Author(s).

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Auteurs

Halvard Bonig (H)

Faculty of Medicine, Institute for Transfusion Medicine and Immunohematology, Goethe University, Frankfurt, Germany.
German Red Cross Blood Service BaWüHe, Institute Frankfurt, Frankfurt, Germany.
Department of Medicine, Division of Hematology, University of Washington, Seattle, WA, USA.

Mareike Verbeek (M)

School of Medicine, Technical University Munich, Klinikum Rechts Der Isar, Clinic and Policlinic for Internal Medicine III, Munich, Germany.

Peter Herhaus (P)

School of Medicine, Technical University Munich, Klinikum Rechts Der Isar, Clinic and Policlinic for Internal Medicine III, Munich, Germany.

Krischan Braitssch (K)

School of Medicine, Technical University Munich, Klinikum Rechts Der Isar, Clinic and Policlinic for Internal Medicine III, Munich, Germany.

Gernot Beutel (G)

Hannover Medical School, Department of Hematology, and Stem Cell Transplantation, HemostasisHannover, Oncology, Germany.

Christoph Schmid (C)

Augsburg University Hospital and Medical Faculty, Augsburg, Germany.

Nadine Müller (N)

Universitätsklinikum Mannheim, Mannheim, Germany.

Gesine Bug (G)

Department of Medicine 2, University Hospital, Goethe University, Frankfurt, Germany.

Michaela Döring (M)

Universitätsklinik Für Kinder Und Jugendmedizin, Tübingen, Germany.

Arend von Stackelberg (A)

Charité, Universitätsmedizin Berlin, Berlin, Germany.

Johanna Tischer (J)

Department of Medicine III, LMU University Hospital, LMU Munich, Munich, Germany.

Francis Ayuk (F)

Klinik Für Stammzelltransplantation, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

Gerald Wulf (G)

Hämatologie Und Medizinische Onkologie, Universitätsmedizin Göttingen, Göttingen, Germany.

Udo Holtick (U)

Universitätsklinikum Köln, Cologne, Germany.

Lisa-Marie Pfeffermann (LM)

German Red Cross Blood Service BaWüHe, Institute Frankfurt, Frankfurt, Germany.

Bernd Jahrsdörfer (B)

Institute for Clinical Transfusion Medicine and Immunogenetics, University of Ulm, Ulm, Germany.

Hubert Schrezenmeier (H)

Institute for Clinical Transfusion Medicine and Immunogenetics, University of Ulm, Ulm, Germany.

Selim Kuci (S)

Department of Pediatrics, Division for Stem Cell Transplantation and Immunology, Goethe University, Frankfurt, Germany.

Zyrafete Kuci (Z)

Department of Pediatrics, Division for Stem Cell Transplantation and Immunology, Goethe University, Frankfurt, Germany.

Anke Zens (A)

Medac Gesellschaft Für Klinische Spezialpräparate mbH, Wedel, Germany.

Michael Tribanek (M)

Medac Gesellschaft Für Klinische Spezialpräparate mbH, Wedel, Germany.

Robert Zeiser (R)

Department Innere Medizin, Klinik Für Innere Medizin I, Universitätsklinikum Freiburg, Freiburg, Germany.

Sabine Huenecke (S)

Department of Pediatrics, Division of Stem Cell Transplantation and Immunology, Goethe University Frankfurt, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany.

Peter Bader (P)

Department of Pediatrics, Division of Stem Cell Transplantation and Immunology, Goethe University Frankfurt, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Germany. p.bader@em.uni-frankfurt.de.

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