TY - JOUR
T1 - Myeloablative allogeneic versus autologous stem cell transplantation in adult patients with acute lymphoblastic leukemia in first remission
T2 - a prospective sibling donor versus no-donor comparison
AU - Cornelissen, Jan J.
AU - van der Holt, Bronno
AU - Verhoef, Gregor E. G.
AU - van 't Veer, Mars B.
AU - van Oers, Marinus H. J.
AU - Schouten, Harry C.
AU - Ossenkoppele, Gert
AU - Sonneveld, Pieter
AU - Maertens, Johan
AU - Kooy, Marinus van Marwijk
AU - Schaafsma, Martijn R.
AU - Wijermans, Pierre W.
AU - Biesma, Douwe H.
AU - Wittebol, Shulamit
AU - Voogt, Paul J.
AU - Baars, Joke W.
AU - Zachee, Pierre
AU - Verdonck, Leo F.
AU - Lowenberg, Bob
AU - Dekker, Adriaan W.
AU - Dutch-Belgian HOVON Cooperative
AU - Huls, Gerwin
PY - 2009/2/5
Y1 - 2009/2/5
N2 - 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)
AB - 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)
KW - BONE-MARROW-TRANSPLANTATION
KW - MINIMAL RESIDUAL DISEASE
KW - ACUTE MYELOID-LEUKEMIA
KW - TIME QUANTITATIVE PCR
KW - STANDARD-RISK
KW - LALA-94 TRIAL
KW - THERAPY
KW - CHEMOTHERAPY
KW - TARGETS
KW - RELAPSE
U2 - 10.1182/blood-2008-07-168625
DO - 10.1182/blood-2008-07-168625
M3 - Article
SN - 0006-4971
VL - 113
SP - 1375
EP - 1382
JO - Blood
JF - Blood
IS - 6
ER -