Thromboembolic phenomena, frequently observed in children with cancer
who are undergoing chemotherapy, can cause significant morbidity and,
less frequently, mortality. Many contributory factors have been identi
fied. Whether the recently identified and most common coagulation defe
ct predisposing to thrombosis, factor V Leiden, is associated with thr
ombosis in this setting, has not been explored. The current study was
undertaken to determine the prevalence of the factor V Leiden mutation
in children with cancer who developed thromboembolic phenomena as com
pared to those with cancer who did not. Genomic DNA was amplified usin
g the polymerase chain reaction (PCR), followed by digestion of the am
plification product with the restriction enzyme MnlI. The digested PCR
products were then size-fractionated to classify samples as heterozyg
ous, homozygous or normal for the factor V Leiden mutation. 67 childre
n with cancer were evaluated for the factor V Leiden mutation. One of
32 children with cancer and thrombosis, and none of 35 who had not exp
erienced thrombotic problems, was found heterozygous for this mutation
. We conclude that the factor V Leiden mutation does not play a signif
icant role in the overall incidence of thromboses that occur in childr
en with cancer.