INCIDENCE AND CHARACTERIZATION OF SECONDARY MYELODYSPLASTIC SYNDROME AND ACUTE MYELOGENOUS LEUKEMIA FOLLOWING HIGH-DOSE CHEMORADIOTHERAPY AND AUTOLOGOUS STEM-CELL TRANSPLANTATION FOR LYMPHOID MALIGNANCIES
Dl. Darrington et al., INCIDENCE AND CHARACTERIZATION OF SECONDARY MYELODYSPLASTIC SYNDROME AND ACUTE MYELOGENOUS LEUKEMIA FOLLOWING HIGH-DOSE CHEMORADIOTHERAPY AND AUTOLOGOUS STEM-CELL TRANSPLANTATION FOR LYMPHOID MALIGNANCIES, Journal of clinical oncology, 12(12), 1994, pp. 2527-2534
Purpose: To analyze the risk of developing myelodysplastic syndrome (M
DS) or acute myelogenous leukemia (AML) following autologous bone marr
ow transplantation (ABMT) or peripheral stem-cell transplantation (PSC
T) and to determine the impact on failure-free survival (FFS). Patient
s and Methods: patients underwent ABMT or PSCT for the treatment of Ho
dgkin's disease (HD) and non-Hodgkin's lymphoma (NHL) at the Universit
y of Nebraska Medical Center. For those patients who went on to develo
p MDS/AML, controls were selected and a case-control-within-a-cohort s
tudy undertaken. Results: Twelve patients developed MDS or AML a media
n of 44 months following ABMT/PSCT. The cumulative incidence (P =.42)
and the conditional probability (P =.32) of MDS/AML were not statistic
ally different between HD and NHL patients. Age greater than 40 years
at the time of transplant (P =.05) and receipt of a total-body irradia
tion (TBI)-containing regimen (P =.06) were predictive for developing
MDS/AML in patients with NHL. Conclusion: There is an increased risk o
f MDS/AML following AMBT/PSCT for lymphoid malignancies. NHL patients
age greater than or equal to 40 years at the time of transplant and wh
o received TBI are at greatest risk. (C) 1994 by American Society of C
linical Oncology.