Therapy of chronic myelogenous leukemia with allogeneic bone marrow transplantation.
- 1 July 1987
- journal article
- research article
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 5 (7) , 1033-1040
- https://doi.org/10.1200/jco.1987.5.7.1033
Abstract
From December 1982 to January 1986, 57 patients received allogeneic bone marrow transplantation as therapy for Philadelphia chromosome (Ph'') positive chronic myelogenous leukemia (CML). All patients were prepared for transplantation with cyclophosphamide 60 mg/kg (day -6, -5) and fractionated total body irradiation, 165 cGy twice daily (day -4, -3, -2, -1) and received major histocompatibility (MHC) matched donor marrow (day 0). All patients received graft-v-host disease (GVHD) prophylaxis with methotrexate, prednisone, and either antithymocyte globulin (ATG) (55 patients) or OKT3 infusion (two patients). The projected survival of 29 chronic phase patients is 64% (95% confidence interval [CI] 42% to 86%); and of 28 accelerated phase patients, 30% (95% CI, 12% to 48%) at 30 months (P = .005). Multivariate regression analysis of pretransplant patient characteristics demonstrated that the presence of chronic phase and age < 30 years were the only prognostic features studied that independently predicted survival. No evidence of persistent or recurrent disease has occurred in chronic phase patients; however, reappearance of the Ph'' was observed in seven accelerated-phase patients, and hematologic relapse occurred in three of these seven patients. The incidence of grade II to IV acute GVHD is 63% (95% CI, 50% to 76%) at 100 days, and that of extensive chronic GVHD is 53% (95% CI, 33% to 74%) at 30 months. The median Karnofsky activity assessment of survivors is 100% (range, 60% to 100%), and all activity assessments > 100% can be attributed to complications of GVHD. Bone marrow transplantation therapy for CML after preparation with cyclophosphamide and fractionated total body irradiation results in a high proportion of disease-free survival in chronic-phase patients. Survival in accelerated phase is significantly worse and is associated with relapse. GVHD has emerged as a significant cause of morbidity and mortality in this study.This publication has 18 references indexed in Scilit:
- Treatment of Donor Bone Marrow with Monoclonal Anti-T-Cell Antibody and Complement for the Prevention of Graft-Versus-Host DiseaseAnnals of Internal Medicine, 1986
- Marrow Transplantation for the Treatment of Chronic Myelogenous LeukemiaAnnals of Internal Medicine, 1986
- Fatal Epstein-Barr-Virus-Associated Proliferation of Donor B Cells After Treatment of Acute Graft-Versus-Host Disease with a Murine Anti-T-Cell AntibodyAnnals of Internal Medicine, 1984
- MARROW TRANSPLANTATION FOR PATIENTS IN THE CHRONIC PHASE OF CHRONIC GRANULOCYTIC LEUKAEMIAThe Lancet, 1982
- SUCCESSFUL ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR PATIENTS IN THE ACCELERATED PHASE OF CHRONIC GRANULOCYTIC LEUKAEMIAThe Lancet, 1982
- A Randomized Study of the Prevention of Acute Graft-versus-Host DiseaseNew England Journal of Medicine, 1982
- Treatment of Chronic Granulocytic Leukemia with Chemoradiotherapy and Transplantation of Marrow from Identical TwinsNew England Journal of Medicine, 1982
- POLYMORPHIC DIFFUSE B-CELL HYPERPLASIAS AND LYMPHOMAS IN RENAL-TRANSPLANT RECIPIENTS1981
- CYTOGENETIC CONVERSION FOLLOWING ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR ADVANCED CHRONIC MYELOGENOUS LEUKEMIA1981
- Chronic graft-versus-host syndrome in manThe American Journal of Medicine, 1980