Relapse of aplastic anaemia after immunosuppressive treatment: a report from the European Bone Marrow Transplantation Group SAA Working Party
- 1 October 1993
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 85 (2) , 371-377
- https://doi.org/10.1111/j.1365-2141.1993.tb03181.x
Abstract
Summary This study was designed to determine the incidence of relapse and factors predictive for relapse in 719 patients with severe aplastic anaemia (SAA) after immunosuppressive treatment (IS). Patients developing myelodysplasia or acute leukaemia after IS, and patients receiving a transplant, were excluded from this analysis. Response was defined as reaching complete independence from transfusions, relapse was defined as becoming again transfusion dependent. This criteria was validated by similar figures when using other ‘relapse criteria’ such as drop in neutrophil or platelet counts. Of 358 patients responding to IS, 74 patients relapsed after a mean time of 778 d after treatment. The actuarial incidence of relapse is 35.2% at 14 years after IS. The risk for relapse was higher in patients responding within 120 d from IS (48%) compared to patients responding between 120 and 360 d (40%) and only 20% for slow responders (>360d from IS) (PPv 134 d, P=0.037). Relapse was not predicted by the severity of the disease, age, and sex. In 39 of the 74 relapsing patients a second response could be achieved. Responses after relapse were associated in univariate analysis with early response to previous IS and early occurrence of relapse. The actuarial survival of patients not relapsing is significantly better than survival of patients relapsing (79.8%v 67.1%, P = 0.0024). However, the actuarial survival of 39 relapsing patients who responded again to IS was similar to patients not relapsing (86%) and significantly better than in 35 patients not reaching a second response after relapse (49.3%, P=0.0015). This study indicates that relapse is a relevant problem in the treatment of aplastic anaemia, and does have an impact on overall survival. Prospective studies of immunosuppressive regimens, looking at responses, should also address this problem in the future.Keywords
This publication has 27 references indexed in Scilit:
- Treatment of severe aplastic anemia by bone marrow transplantationHematological Oncology, 2006
- Secondary Cancers after Bone Marrow Transplantation for Leukemia or Aplastic AnemiaNew England Journal of Medicine, 1989
- Thyroid and pituitary function following allogeneic bone marrow transplantationArchives of internal medicine (1960), 1988
- Re-treatment of aplastic anemia with antithymocyte globulin or antilymphocyte serumThe American Journal of Medicine, 1988
- Myelopoiesis and erythropoiesis of bone marrow cells cultured in vitro in patients recovered from aplastic anaemiaScandinavian Journal of Haematology, 1985
- BONE MARROW TRANSPLANTATION: A REVIEW OF DELAYED COMPLICATIONSBritish Journal of Haematology, 1984
- Aplastic anaemia: an analysis of 174 patientsPostgraduate Medical Journal, 1980
- Granulocytic Progenitor Cells in Aplastic AnaemiaBritish Journal of Haematology, 1977
- Acquired Aplastic Anaemia in AdultsActa Haematologica, 1977
- Nonparametric Estimation from Incomplete ObservationsJournal of the American Statistical Association, 1958