Allogeneic bone marrow transplantation for low-grade lymphoma.

Koen van Besien(Medical College of Wisconsin), Kathleen A. Sobocinski(Medical College of Wisconsin), Philip A. Rowlings(Medical College of Wisconsin), Sandra Murphy(Medical College of Wisconsin), Jamés O. Armitage(Medical College of Wisconsin), Michael R. Bishop(Medical College of Wisconsin), Ok-Kyong Chaekal(Medical College of Wisconsin), Robert Peter Gale(Medical College of Wisconsin), John P. Klein(Medical College of Wisconsin), Hillard M. Lazarus(Medical College of Wisconsin), Philip L. McCarthy(Medical College of Wisconsin), John Raemaekers(Medical College of Wisconsin), Josy Reiffers(Medical College of Wisconsin), Gordon L. Phillips(Medical College of Wisconsin), A Schattenberg(Medical College of Wisconsin), Leo F. Verdonck(Medical College of Wisconsin), Julie M. Vose(Medical College of Wisconsin), Mary M. Horowitz(Medical College of Wisconsin)
PubMed
September 1, 1998
Cited by 265

Abstract

Advanced low-grade lymphomas are usually incurable with conventional-dose chemotherapy. It is uncertain whether cures are possible with high-dose therapy and bone marrow transplant from a human leukocyte antigen (HLA)-identical sibling. We sought to determine the outcome of HLA-identical sibling bone marrow transplants in advanced low-grade lymphoma in an observational study of 113 patients conducted at 50 centers participating in the International Bone Marrow Transplant Registry (IBMTR). The median patient age was 38 years (range, 15 to 61). Eighty percent had stage IV disease at the time of transplantation. The median number of prior chemotherapy regimens was two (range, 0 to 5). Thirty-eight percent had refractory disease and 29% a Karnofsky performance score (KPS) less than 80%. All patients underwent allogeneic bone marrow transplantation from a HLA-identical sibling donor. The conditioning regimen included total-body irradiation (TBI) in 82% of patients; cyclosporine was used for graft-versus-host disease prophylaxis in 74%. Survival, disease-free survival, recurrence rate, treatment-related mortality, and causes of death were determined. Three-year probabilities of recurrence, survival, and disease-free survival were 16% (95% confidence interval [CI], 9% to 27%), 49% (95% CI, 39% to 60%), and 49% (95% CI, 39% to 59%), respectively. Higher survival was associated with pretransplant KPS >/=90%, chemotherapy-sensitive disease, use of a TBI-containing conditioning regimen, and age less than 40 years. We conclude that high-dose therapy followed by transplantation from a HLA-identical sibling leads to prolonged survival in some patients with advanced low-grade lymphoma. Most mortality is treatment-related, and recurrences are rare.


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