Results of a multicenter phase I/II trial of TCR alpha beta and CD19-depleted haploidentical hematopoietic stem cell transplantation for adult and pediatric patients

  • Wolfgang A. Bethge*
  • , Matthias Eyrich
  • , Stephan Mielke
  • , Roland Meisel
  • , Dietger Niederwieser
  • , Paul G. Schlegel
  • , Ansgar Schulz
  • , Johann Greil
  • , Donald Bunjes
  • , Arne Brecht
  • , Jurgen Kuball
  • , Michael Schumm
  • , Vladan Vucinic
  • , Markus Wiesneth
  • , Halvard Bonig
  • , Kasper Westinga
  • , Stefanie Biedermann
  • , Silke Holtkamp
  • , Sandra Karitzky
  • , Michaela Malchow
  • Christiane Siewert, Rupert Handgretinger, Peter Lang
*Corresponding author for this work

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Abstract

Hematopoietic stem cell transplantation (HSCT) from haploidentical donors is a viable option for patients lacking HLA-matched donors. Here we report the results of a prospective multicenter phase I/II trial of transplantation of TCRαβ and CD19-depleted peripheral blood stem cells from haploidentical family donors after a reduced-intensity conditioning with fludarabine, thiotepa, and melphalan. Thirty pediatric and 30 adult patients with acute leukemia (n = 43), myelodysplastic or myeloproliferative syndrome (n = 6), multiple myeloma (n = 1), solid tumors (n = 6), and non-malignant disorders (n = 4) were enrolled. TCR αβ/CD19-depleted grafts prepared decentrally at six manufacturing sites contained a median of 12.1 × 106 CD34+ cells/kg and 14.2 × 103 TCRαβ+ T-cells/kg. None of the patients developed grade lll/IV acute graft-versus-host disease (GVHD) and only six patients (10%) had grade II acute GVHD. With a median follow-up of 733 days 36/60 patients are alive. The cumulative incidence of non-relapse mortality at day 100, 1 and 2 years after HSCT was 5%, 15%, and 17% for all patients, respectively. Estimated probabilities of overall and disease-free survival at 2 years were 63% and 50%, respectively. Based on these promising results in a high-risk patient cohort, haploidentical HSCT using TCRαβ/CD19-depleted grafts represents a viable treatment option.

Original languageEnglish
Pages (from-to)423-430
Number of pages8
JournalBone Marrow Transplantation
Volume57
Issue number3
Early online date24 Dec 2021
DOIs
Publication statusPublished - Mar 2022

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