TY - JOUR
T1 - Thiotepa-based versus total body irradiation-based myeloablative conditioning prior to allogeneic stem cell transplantation for acute myeloid leukaemia in first complete remission
T2 - A retrospective analysis from the Acute Leukemia Working Party of the European Group for Blood and Marrow Transplantation
AU - Acute Leukemia Working Party
AU - Eder, Sandra
AU - Labopin, Myriam
AU - Arcese, William
AU - Or, Reuven
AU - Majolino, Ignazio
AU - Bacigalupo, Andrea
AU - de Rosa, Gennaro
AU - Volin, Liisa
AU - Beelen, Dietrich
AU - Veelken, Hendrik
AU - Schaap, Nicolaas P.M.
AU - Kuball, Jurgen
AU - Cornelissen, Jan
AU - Nagler, Arnon
AU - Mohty, Mohamad
N1 - Publisher Copyright:
© 2016 John Wiley & Sons A/S.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Thiotepa is an alkylating compound with an antineoplastic and myeloablative activity and can mimic the effect of radiation. However, it is unknown whether this new regimen could safely replace the long-established ones. This retrospective matched-pair analysis evaluated the outcome of adults with acute myeloid leukaemia in first complete remission who received myeloablative conditioning either with a thiotepa-based (n=121) or a cyclophosphamide/total body irradiation-based (TBI; n=358) regimen for allogeneic hematopoietic stem cell transplantation from an HLA-matched sibling or an unrelated donor. With a median follow-up of 44months, the outcome was similar in both groups. Acute graft-versus-host disease grade II-IV was observed in 25% after thiotepa-containing regimen versus 35% after TBI (P=0.06). The 2-yr cumulative incidence of chronic graft-versus-host disease was 40.5% for thiotepa and 41% for TBI (P=0.98). At 2 yrs, the cumulative incidences of non-relapse mortality and relapse incidence were 23.9% (thiotepa) vs. 22.4% (TBI; P=0.66) and 17.2% (thiotepa) vs. 23.3% (TBI; P=0.77), respectively. The probabilities of leukaemia-free and overall survival at 2yrs were not significantly different between the thiotepa and TBI groups, at 58.9% vs. 54.2% (P=0.95) and 61.4% vs. 58% (P=0.72), respectively. Myeloablative regimens using combinations including thiotepa can provide satisfactory outcomes, but the optimal conditioning remains unclear for the individual patient in this setting.
AB - Thiotepa is an alkylating compound with an antineoplastic and myeloablative activity and can mimic the effect of radiation. However, it is unknown whether this new regimen could safely replace the long-established ones. This retrospective matched-pair analysis evaluated the outcome of adults with acute myeloid leukaemia in first complete remission who received myeloablative conditioning either with a thiotepa-based (n=121) or a cyclophosphamide/total body irradiation-based (TBI; n=358) regimen for allogeneic hematopoietic stem cell transplantation from an HLA-matched sibling or an unrelated donor. With a median follow-up of 44months, the outcome was similar in both groups. Acute graft-versus-host disease grade II-IV was observed in 25% after thiotepa-containing regimen versus 35% after TBI (P=0.06). The 2-yr cumulative incidence of chronic graft-versus-host disease was 40.5% for thiotepa and 41% for TBI (P=0.98). At 2 yrs, the cumulative incidences of non-relapse mortality and relapse incidence were 23.9% (thiotepa) vs. 22.4% (TBI; P=0.66) and 17.2% (thiotepa) vs. 23.3% (TBI; P=0.77), respectively. The probabilities of leukaemia-free and overall survival at 2yrs were not significantly different between the thiotepa and TBI groups, at 58.9% vs. 54.2% (P=0.95) and 61.4% vs. 58% (P=0.72), respectively. Myeloablative regimens using combinations including thiotepa can provide satisfactory outcomes, but the optimal conditioning remains unclear for the individual patient in this setting.
KW - Acute myeloid leukaemia
KW - Allo-HSCT
KW - Thiotepa
KW - Total body irradiation
UR - http://www.scopus.com/inward/record.url?scp=84955208995&partnerID=8YFLogxK
U2 - 10.1111/ejh.12553
DO - 10.1111/ejh.12553
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C2 - 25807864
AN - SCOPUS:84955208995
SN - 0902-4441
VL - 96
SP - 90
EP - 97
JO - European Journal of Haematology
JF - European Journal of Haematology
IS - 1
ER -