[HTML][HTML] Randomized trial of allogeneic related bone marrow transplantation versus peripheral blood stem cell transplantation for chronic myeloid leukemia

VG Oehler, JP Radich, B Storer, KG Blume… - Biology of Blood and …, 2005 - Elsevier
VG Oehler, JP Radich, B Storer, KG Blume, T Chauncey, R Clift, DS Snyder, SJ Forman…
Biology of Blood and Marrow Transplantation, 2005Elsevier
Seventy-two chronic myeloid leukemia patients were enrolled as part of a larger randomized
trial at 3 centers between March 1996 and July 2001 to undergo either HLA-matched related
allogeneic bone marrow (BM) or filgrastim (granulocyte colony-stimulating factor)-mobilized
peripheral blood stem cell (PBSC) transplantation. Forty patients received BM, and 32
patients received PBSCs. There was no statistically significant difference in the incidence of
acute or chronic graft-versus-host disease (GVHD), overall survival, disease-free survival, or …
Seventy-two chronic myeloid leukemia patients were enrolled as part of a larger randomized trial at 3 centers between March 1996 and July 2001 to undergo either HLA-matched related allogeneic bone marrow (BM) or filgrastim (granulocyte colony-stimulating factor)-mobilized peripheral blood stem cell (PBSC) transplantation. Forty patients received BM, and 32 patients received PBSCs. There was no statistically significant difference in the incidence of acute or chronic graft-versus-host disease (GVHD), overall survival, disease-free survival, or non-relapse-related mortality between patients receiving BM or PBSC transplants. The cumulative incidence of grade II to IV acute GVHD was 49% in BM and 55% in PBSC recipients (P = .48). The cumulative incidence of clinical extensive chronic GVHD was 50% in BM and 59% in PBSC recipients (P = .46). Among 62 chronic phase chronic myeloid leukemia patients, there was no significant difference in overall survival (87% versus 81%; P = .59), disease-free survival (80% versus 81%; P = .61), or non-relapse-related mortality (13% versus 19%; P = .60) by cell source (BM versus PBSCs). Among chronic phase patients, however, there was a trend toward a higher cumulative incidence of relapse at 3 years in BM recipients (7% versus 0%; P = .10) and a higher cumulative incidence of chronic GVHD in PBSC recipients (59% versus 40%; P = .11). The trend toward a higher relapse incidence in BM recipients persisted with a longer follow-up.
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