Treosulfan–fludarabine–thiotepa-based conditioning treatment before allogeneic hematopoietic stem cell transplantation for pediatric patients with hematological malignancies

Krzysztof Kalwak, Monika Mielcarek, Katharine Patrick, Jan Styczynski, Peter Bader, Selim Corbacioglu, Birgit Burkhardt, Karl Walter Sykora, Katarzyna Drabko, Jolanta Gozdzik, Franca Fagioli, Johann Greil, Bernd Gruhn, Rita Beier, Franco Locatelli, Ingo Müller, Paul Gerhardt Schlegel, Petr Sedlacek, Klaus Daniel Stachel, Claudia HemmelmannAnn-Kristin Möller, Joachim Baumgart, Ajay Vora

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

Treosulfan-based conditioning prior to allogeneic transplantation has been shown to have myeloablative, immunosuppressive, and antineoplastic effects associated with reduced non-relapse mortality (NRM) in adults. Therefore, we prospectively evaluated the safety and efficacy of treosulfan-based conditioning in children with hematological malignancies in this phase II trial. Overall, 65 children with acute lymphoblastic leukemia (35.4%), acute myeloid leukemia (44.6%), myelodysplastic syndrome (15.4%), or juvenile myelomonocytic leukemia (4.6%) received treosulfan intravenously at a dose of 10 mg/m2/day (7.7%), 12 g/m2/day (35.4%), or 14 g/m2/day (56.9%) according to their individual body surface area in combination with fludarabine and thiotepa. The incidence of complete donor chimerism at day +28 was 98.4% with no primary and only one secondary graft failure. At 36 months, NRM was only 3.1%, while relapse incidence was 21.7%, and overall survival was 83.0%. The cumulative incidence of acute graft-vs.-host disease was 45.3% for grades I–IV and 26.6% for grades II–IV. At 36 months, 25.8% overall and 19.4% moderate/severe chronic graft-vs.-host disease were reported. These data confirm the safe and effective use of treosulfan-based conditioning in pediatric patients with hematological malignancies. Therefore, treosulfan/fludarabine/thiotepa can be recommended for myeloablative conditioning in children with hematological malignancies.
Lingua originaleEnglish
pagine (da-a)1996-2007
Numero di pagine12
RivistaBone Marrow Transplantation
Volume55
DOI
Stato di pubblicazionePubblicato - 2020

Keywords

  • HSCT

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