P. Shearer et al., Secondary acute myelogenous leukemia in patients previously treated for childhood renal tumors: A report from the National Wilms Tumor Study Group, J PED H ONC, 23(2), 2001, pp. 109-111
Purpose: This review characterized cases of secondary acute myelogenous leu
kemia (AML) occurring after treatment of renal neoplasms on protocols of th
e National Wilms Tumor Study Group (NWTSG) between October 1969 and Decembe
r 1991.
Patients and Methods: The NWTSG database was reviewed for cases of secondar
y AML and for WT1 status of the affected patients. Referring institutions w
ere contacted by a confidential letter requesting pathology reports, result
s of immunophenotyping. cytogenetic, and molecular analyses, and details co
ncerning treatment of AML.
Results: Of the 5,278 patients treated during the study period, 43 had seco
nd malignant neoplasms, and 7 of these 43 had AML. At the time of diagnosis
of Wilms tumor. the median age of the seven patients (4 boys) was 3.2 year
s. Five of the seven renal neoplasms had favorable histologic characteristi
cs. The most common French-American-British morphology was M5. One patient
had bilateral tumors, and two were treated for recurrent Wilms tumor. All p
atients received chemotherapy regimens that included doxorubicin (6) or eto
poside (I), and six were treated with infradiaphragmatic irradiation. The m
edian latency period from initial diagnosis of the renal neoplasm to develo
pment of secondary AML was 3 years (range, 1.2-4 yrs). One patient had the
translocation t(9;11)(p22:q23); WT1 status was not noted for any of the sev
en patients.
Conclusions: The development of secondary AML in this subset of patients af
ter treatment of renal neoplasms may reflect the interaction of the effects
of treatment and possible genetic predisposition toward cancer.