Impact of conditioning with TBI in adult patients with T-cell ALL who receive a myeloablative allogeneic stem cell transplantation: a report from the acute leukemia working party of EBMT

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • X Cahu
  • M Labopin
  • S Giebel
  • M Aljurf
  • S Kyrcz-Krzemien
  • G Socié
  • M Eder
  • F Bonifazi
  • D Bunjes
  • S Vigouroux
  • M Michallet
  • M Stelljes
  • T Zuckerman
  • J Finke
  • J Passweg
  • I Yakoub-Agha
  • D Niederwieser
  • G Sucak
  • Sengeløv, Henrik
  • E Polge
  • A Nagler
  • J Esteve
  • M Mohty
  • Acute Leukemia Working Party of EBMT

Allogeneic hematopoietic stem cell transplantation (allo-SCT) is a therapeutic option for adult patients with T-cell ALL (T-ALL). Meanwhile, few allo-SCT data specific to adult T-ALL have been described thus far. Specifically, the optimal myeloablative conditioning regimen is unknown. In this retrospective study, 601 patients were included. Patients received allo-SCT in CR1, CR2, CR >2 or in advanced disease in 69%, 15%, 2% and 14% of cases, respectively. With an overall follow-up of 58 months, 523 patients received a TBI-based regimen, whereas 78 patients received a chemotherapy-based regimen including IV busulfan-cyclophosphamide (IV Bu-Cy) (n=46). Unlike patients aged ⩾35 years, patients aged <35 years who received a TBI-based regimen displayed an improved outcome compared with patients who received a chemotherapy-based regimen (5-year leukemia-free survival (LFS) of 50% for TBI versus 18% for chemo-only regimen or IV Bu-Cy regimens, P=10(-5) and 10(-4), respectively). In multivariate analysis, use of TBI was associated with an improved LFS (hazard ratio (HR)=0.55 (0.34-0.86), P=0.01) and overall survival (HR=0.54 (0.34-0.87), P=0.01) in patients aged <35 years. In conclusion, younger adult patients with T-ALL entitled to receive a myeloablative allo-SCT may benefit from TBI-based regimens.

OriginalsprogEngelsk
TidsskriftBone
Vol/bind51
Sider (fra-til)351-357
Antal sider7
ISSN8756-3282
DOI
StatusUdgivet - 2016
Eksternt udgivetJa

ID: 174235442