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

Wolfgang Bethge(STZ eyetrial), Matthias Eyrich, Stephan Mielke(Karolinska University Hospital), Roland Meisel(Heinrich Heine University Düsseldorf), Dietger Niederwieser(Leipzig University), Paul G. Schlegel, Ansgar Schulz, Johann Greil(Heidelberg University), Donald Bunjes(Universität Ulm), Arne Brecht(Helios Dr. Horst Schmidt Kliniken Wiesbaden), Jürgen Kuball(University Medical Center Utrecht), Michael Schumm(CureVac (Germany)), Vladan Vučinić(Leipzig University), Markus Wiesneth(Universität Ulm), Halvard Bönig(Goethe University Frankfurt), Kasper Westinga(University Medical Center Utrecht), S. Biedermann(Miltenyi Biotec (Germany)), Silke Holtkamp(Miltenyi Biotec (Germany)), Sandra Karitzky(Miltenyi Biotec (Germany)), Michaela Malchow(Miltenyi Biotec (Germany)), Christiane Siewert(Miltenyi Biotec (Germany)), Rupert Handgretinger(University Children's Hospital Tübingen), Peter Lang(University Children's Hospital Tübingen)
Bone Marrow Transplantation
December 24, 2021
Cited by 56Open Access
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Abstract

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 × 10 6 CD34 + cells/kg and 14.2 × 10 3 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.


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