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T-Cell-Depleted Allogeneic Bone Marrow Transplantation as
Postremission Therapy for Acute Myelogenous Leukemia: Freedom From
Relapse in the Absence of Graft-Versus-Host Disease
Esperanza B. Papadopoulos,
Matthew H. Carabasi,
Hugo Castro-Malaspina,
Barrett H. Childs,
Stephen Mackinnon,
Farid Boulad,
Alfred P. Gillio,
Nancy A. Kernan,
Trudy N. Small,
Paul Szabolcs,
Joanne Taylor,
Joachim Yahalom,
Nancy H. Collins,
Sharon
A. Bleau,
Patricia M. Black,
Glenn Heller,
Richard J. O' Reilly, and
James W. Young
From the Allogeneic Bone Marrow Transplantation Service, Division of
Hematologic Oncology, Department of Medicine; the Department of
Pediatrics; the Department of Nursing; the Department of Radiation
Oncology; the Department of Biostatistics and Epidemiology, Memorial
Sloan-Kettering Cancer Center, Cornell University Medical College, New
York; and The Laboratory of Cellular Physiology and Immunology, The
Rockefeller University, New York, NY.
Thirty-one consecutive patients with acute myelogenous leukemia
(AML) in first complete remission and 8 with AML in second complete
remission received T cell-depleted allogeneic bone marrow transplants
from HLA-identical sibling donors. Patients received myeloablative
cytoreduction consisting of hyperfractionated total body irradiation,
thiotepa, and cyclophosphamide. Those patients at risk for
immune-mediated graft rejection received additional immune suppression
with antithymocyte globulin and methylprednisolone in the early
peritransplant period. Patients with AML who underwent allogeneic
T-cell-depleted bone marrow transplantations (BMT) in first or second
remission have achieved respective disease-free survival (DFS)
probabilities of 77% (median follow-up at approximately 56 months) and
50% (median follow-up at approximately 48 months). Ten of 31 patients
transplanted in first remission were 40 years old and have attained
a DFS at 4 years of 70%. For patients with AML transplanted in first
or second remission, the respective cause-specific probabilities of
relapse were 3.2% or 12.5%, and those of nonleukemic mortality were
19.4% or 37.5%. There were no cases of immune-mediated graft
rejection and no cases of grade II to IV acute graft-versus-host
disease (GVHD). All survivors enjoy Karnofsky performance scores (KPS)
of 100%, except 2 patients with KPS of 80% to 90%.
T-cell-depleted allogeneic BMT can provide durable DFS together with
an excellent performance status in the majority of patients with de
novo AML. In addition, GVHD is not an obligatory correlate of the
graft-versus-leukemia benefit or freedom from relapse afforded by
allogeneic BMT administered as postremission therapy for AML. This
study provides a basis for prospective comparison with other
postremission therapies considered standard in the management of
patients with this disease.
Blood, Vol. 91 No. 3 (February 1), 1998:
pp. 1083-1090
© 1998 by The American Society of Hematology.

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