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Prepublished online as a Blood First Edition Paper on November 27, 2002; DOI 10.1182/blood-2002-05-1483.
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Blood, 1 April 2003, Vol. 101, No. 7, pp. 2476-2482
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS
A comparison of allogeneic and autologous bone marrow
transplantation for lymphoblastic lymphoma
John E. Levine,
Richard E. Harris,
Fausto R. Loberiza Jr,
James O. Armitage,
Julie M. Vose,
Koen Van
Besien,
Hillard M. Lazarus, and
Mary M. Horowitz on behalf of the
Lymphoma Study Writing Committee of the International Bone Marrow
Transplant Registry and Autologous Blood and Marrow Transplant
Registry
From the University of Michigan Medical Center, Ann
Arbor; Children's Hospital Medical Center, Cincinnati, OH;
International Bone Marrow Transplant Registry/Autologous Bone Marrow
Transplant Registry, Health Policy Institute, Medical College of
Wisconsin, Milwaukee; University of Nebraska Medical Center, Omaha;
Case Western Reserve University, Cleveland, OH; University of Chicago,
IL.
Lymphoblastic lymphoma (LBL) is a rare, clinically aggressive
neoplasm of the young that frequently involves the bone marrow (BM)
and/or central nervous system. Because LBL is similar to acute
lymphoblastic leukemia, some centers prefer allogeneic hematopoietic stem cell (SC) transplantation to autologous SC
transplantation. We retrospectively analyzed outcomes for patients who
underwent autologous (auto, n = 128) or HLA-identical sibling
(allo, n = 76) SC transplantations from 1989 to 1998 and were
reported to International Bone Marrow Transplant Registry
(IBMTR) or Autologous Blood and Marrow Transplant Registry
(ABMTR). Allo stem cell transplant (SCT) recipients had higher
treatment-related mortality (TRM) at 6 months (18% versus
3%, P = .002), and this disadvantage persisted at 1 and
5 years. Early relapse rates after alloSC transplantation and
autoSC transplantation were similar, but significantly lower relapse
rates were observed in alloSCT recipients at 1 and 5 years (32% versus
46%, P = .05; and 34% versus 56%,
P = .004, respectively). No differences were noted in
lymphoma-free survival rates between alloSC transplantations and
autoSC transplantations (5-year rates 36% versus 39%,
P = .82). AutoSCT recipients had higher overall survival at 6 months (75% versus 59%, P = .01), but
survival did not significantly differ between the 2 groups at 1 and 5 years (60% versus 49%, P = .09; 44% versus 39%,
P = .47, respectively). Multivariate analyses to account
for confounding factors confirmed these results. Independent of SCT
type, BM involvement at the time of transplantation and disease status
more advanced than first complete remission were associated with
inferior outcomes. In summary, alloSC transplantation for LBL is
associated with fewer relapses than with autoSC transplantation, but
higher TRM offsets any potential survival benefit.

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