TY - JOUR
T1 - Long-Term Outcomes of Alemtuzumab-Based Reduced-Intensity Conditioned Hematopoietic Stem Cell Transplantation for Myelodysplastic Syndrome and Acute Myelogenous Leukemia Secondary to Myelodysplastic Syndrome
AU - Potter, Victoria T.
AU - Krishnamurthy, Pramila
AU - Barber, Linda D.
AU - Lim, ZiYi
AU - Kenyon, Michelle
AU - Ireland, Robin M.
AU - de Lavallade, Hugues
AU - Dhouri, Abdel
AU - Marsh, Judith C.W.
AU - Marcus, Robert
AU - Devereux, Stephen
AU - Ho, Aloysius
AU - Pagliuca, Tony
AU - Mufti, Ghulam J.
PY - 2014/1
Y1 - 2014/1
N2 - Allogeneic hematopoietic stem cell transplantation (HSCT) with reduced-intensity conditioning (RIC) offers a potential cure for patients with myelodysplastic syndrome (MDS) who are ineligible for standard-intensity regimens. Previously published data from our institution suggest excellent outcomes at 1 yr using a uniform fludarabine, busulfan, and alemtuzumab-based regimen. Here we report long-term follow-up of 192 patients with MDS and acute myelogenous leukemia (AML) secondary to MDS (MDS-AML) transplanted with this protocol, using sibling (n = 45) or matched unrelated (n = 147) donors. The median age of the cohort was 57 yr (range, 21 to 72 yr), and median follow-up was 4.5 yr (range, 0.1 to 10.6 yr). The 5-yr overall survival (OS), event-free survival, and nonrelapse mortality were 44%, 33%, and 26% respectively. The incidence of de novo chronic graft-versus-host disease (GVHD) was low at 19%, illustrating the efficacy of alemtuzumab for GVHD prophylaxis. Conversely, the 5-yr relapse rate was 51%. For younger patients (age 60 yr having a 5-yr OS of 15% and relapse rate of 66%. Patients receiving preemptive donor lymphocyte infusions had an impressive 5-yr OS of 67%, suggesting that this protocol may lend itself to the incorporation of immunotherapeutic strategies. Overall, these data demonstrate good 5-yr OS for patients with MDS and MDS-AML undergoing alemtuzumab-based RIC-HSCT. The low rate of chronic GVHD is encouraging, and comparative studies with other RIC protocols are warranted.
AB - Allogeneic hematopoietic stem cell transplantation (HSCT) with reduced-intensity conditioning (RIC) offers a potential cure for patients with myelodysplastic syndrome (MDS) who are ineligible for standard-intensity regimens. Previously published data from our institution suggest excellent outcomes at 1 yr using a uniform fludarabine, busulfan, and alemtuzumab-based regimen. Here we report long-term follow-up of 192 patients with MDS and acute myelogenous leukemia (AML) secondary to MDS (MDS-AML) transplanted with this protocol, using sibling (n = 45) or matched unrelated (n = 147) donors. The median age of the cohort was 57 yr (range, 21 to 72 yr), and median follow-up was 4.5 yr (range, 0.1 to 10.6 yr). The 5-yr overall survival (OS), event-free survival, and nonrelapse mortality were 44%, 33%, and 26% respectively. The incidence of de novo chronic graft-versus-host disease (GVHD) was low at 19%, illustrating the efficacy of alemtuzumab for GVHD prophylaxis. Conversely, the 5-yr relapse rate was 51%. For younger patients (age 60 yr having a 5-yr OS of 15% and relapse rate of 66%. Patients receiving preemptive donor lymphocyte infusions had an impressive 5-yr OS of 67%, suggesting that this protocol may lend itself to the incorporation of immunotherapeutic strategies. Overall, these data demonstrate good 5-yr OS for patients with MDS and MDS-AML undergoing alemtuzumab-based RIC-HSCT. The low rate of chronic GVHD is encouraging, and comparative studies with other RIC protocols are warranted.
KW - Acute myelogenous leukemia
KW - Myelodysplastic syndrome
KW - Reduced intensity
KW - Transplantatiom
KW - Alemtuzumab
KW - ACUTE MYELOID-LEUKEMIA
KW - BONE-MARROW-TRANSPLANTATION
KW - VERSUS-HOST-DISEASE
KW - IMMUNE RECONSTITUTION
KW - UNRELATED DONORS
KW - ADULT PATIENTS
KW - SURVIVAL
KW - REGIMENS
KW - AGE
KW - REMISSIONS
U2 - 10.1016/j.bbmt.2013.10.021
DO - 10.1016/j.bbmt.2013.10.021
M3 - Article
SN - 1083-8791
VL - 20
SP - 111
EP - 117
JO - BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
JF - BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
IS - 1
ER -