Journal of Translational Medicine (Nov 2023)

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

  • Halvard Bonig,
  • Mareike Verbeek,
  • Peter Herhaus,
  • Krischan Braitssch,
  • Gernot Beutel,
  • Christoph Schmid,
  • Nadine Müller,
  • Gesine Bug,
  • Michaela Döring,
  • Arend von Stackelberg,
  • Johanna Tischer,
  • Francis Ayuk,
  • Gerald Wulf,
  • Udo Holtick,
  • Lisa-Marie Pfeffermann,
  • Bernd Jahrsdörfer,
  • Hubert Schrezenmeier,
  • Selim Kuci,
  • Zyrafete Kuci,
  • Anke Zens,
  • Michael Tribanek,
  • Robert Zeiser,
  • Sabine Huenecke,
  • Peter Bader

DOI
https://doi.org/10.1186/s12967-023-04731-1
Journal volume & issue
Vol. 21, no. 1
pp. 1 – 11

Abstract

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Abstract Background Patients with steroid-refractory acute graft-versus-host disease (aGvHD) not tolerating/responding to ruxolitinib (RR-aGvHD) have a dismal prognosis. 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 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 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.

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