Myeloablative allogeneic versus autologous stem cell transplantation in adult patients with acute lymphoblastic leukemia in first remission: a prospective sibling donor versus no-donor comparison

  • Jan J. Cornelissen*
  • , Bronno van der Holt
  • , Gregor E. G. Verhoef
  • , Mars B. van 't Veer
  • , Marinus H. J. van Oers
  • , Harry C. Schouten
  • , Gert Ossenkoppele
  • , Pieter Sonneveld
  • , Johan Maertens
  • , Marinus van Marwijk Kooy
  • , Martijn R. Schaafsma
  • , Pierre W. Wijermans
  • , Douwe H. Biesma
  • , Shulamit Wittebol
  • , Paul J. Voogt
  • , Joke W. Baars
  • , Pierre Zachee
  • , Leo F. Verdonck
  • , Bob Lowenberg
  • , Adriaan W. Dekker
  • Dutch-Belgian HOVON Cooperative
*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    149 Citations (Scopus)

    Abstract

    While commonly accepted in poor-risk acute lymphoblastic leukemia (ALL), the role of allogeneic hematopoietic stem cell transplantation (allo-SCT) is still disputed in adult patients with standard-risk ALL. We evaluated outcome of patients with ALL in first complete remission (CR1), according to a sibling donor versus no-donor comparison. Eligible patients (433) were entered in 2 consecutive, prospective studies, of whom 288 (67%) were younger than 55 years, in CR1, and eligible to receive consolidation by either an autologous SCT or an allo-SCT. Allo-SCT was performed in 91 of 96 patients with a compatible sibling donor. Cumulative incidences of relapse at 5 years were, respectively, 24 and 55% for patients with a donor versus those without a donor (hazard ratio [HR], 0.37; 0.23-0.60; P <.001). Nonrelapse mortality estimated 16% (+/- 4) at 5 years after allo-SCT. As a result, disease-free survival (DFS) at 5 years was significantly better in the donor group: 60 versus 42% in the no-donor group (HR: 0.60; 0.41-0.89; P = .01). After risk-group analysis, improved outcome was more pronounced in standard-risk patients with a donor, who experienced an overall survival of 69% at 5 years (P = .05). In conclusion, standard-risk ALL patients with a sibling donor may show favorable survival following SCT, due to both a strong reduction of relapse and a modest nonrelapse mortality. This trial is registered with http://www.trialregister.nl under trial ID NTR228. (Blood. 2009; 113: 1375-1382)

    Original languageEnglish
    Pages (from-to)1375-1382
    Number of pages8
    JournalBlood
    Volume113
    Issue number6
    DOIs
    Publication statusPublished - 5-Feb-2009

    Keywords

    • BONE-MARROW-TRANSPLANTATION
    • MINIMAL RESIDUAL DISEASE
    • ACUTE MYELOID-LEUKEMIA
    • TIME QUANTITATIVE PCR
    • STANDARD-RISK
    • LALA-94 TRIAL
    • THERAPY
    • CHEMOTHERAPY
    • TARGETS
    • RELAPSE

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