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Haematopoietic stem cell transplantation after reduced intensity conditioning in children and adolescents with chronic myeloid leukaemia: A prospective multicentre trial of the I-BFM Study Group

  • Herbert Pichler*
  • , Petr Sedlacek
  • , Roland Meisel
  • , Rita Beier
  • , Maura Faraci
  • , Krzysztof Kalwak
  • , Marianne Ifversen
  • , Ingo Müller
  • , Jerry Stein
  • , Kim Vettenranta
  • , Gabriele Kropshofer
  • , Alexandra Kolenova
  • , Susanne Karlhuber
  • , Evgenia Glogova
  • , Ulrike Poetschger
  • , Christina Peters
  • , Meinolf Suttorp
  • , Susanne Matthes-Leodolter
  • , Adriana Balduzzi
  • *Corresponding author af dette arbejde
4 Citationer (Scopus)

Abstract

This prospective multicentre trial evaluated the safety and the efficacy of a thiotepa/melphalan-based reduced intensity conditioning (RIC) haematopoietic stem cell transplantation (HSCT) in children and adolescents with chronic myeloid leukaemia (CML) in chronic phase (CP). Thirty-two patients were transplanted from matched siblings or matched unrelated donors. In 22 patients, HSCT was performed due to insufficient molecular response or loss of response to first- or second-generation tyrosine kinase inhibitor (TKI), with pretransplant BCR::ABL1 transcripts ranging between 0.001% and 33%. The protocol included a BCR::ABL1-guided intervention with TKI retreatment in the first year and donor lymphocyte infusions (DLI) in the second-year post-transplant. All patients engrafted. The 1-year transplant-related mortality was 3% (confidence interval [CI]: 0%-6%). After a median follow-up of 6.3 years, 5-year overall survival and event-free survival are 97% (CI: 93%-100%) and 91% (CI: 79%-100%) respectively. The current 5-year leukaemia-free survival with BCR::ABL1 <0.01% is 97% (CI: 88%-100%) and the current TKI- and DLI-free survival is 95% (CI: 85%-100%). The incidence of chronic graft-versus-host disease (GvHD) was 32%, being severe in four patients (13%). At last follow-up, 31 patients are GvHD-free and have stopped immunosuppression. RIC HSCT following pretreatment with TKI is feasible and effective in children and adolescents with CP-CML with an excellent disease-free and TKI-free survival.

OriginalsprogEngelsk
TidsskriftBritish Journal of Haematology
Vol/bind205
Udgave nummer1
Sider (fra-til)268-279
Antal sider12
ISSN0007-1048
DOI
StatusUdgivet - jul. 2024

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