Background. The use of surveillance imaging in children with medulloblastom
a has been criticised. The aim of this study was to determine what proporti
on of relapses are detected by surveillance and whether these are found at
a relatively favourable stage.
Methods. This study was a retrospective review of the medical charts and im
aging studies of 89 patients treated at a single children's cancer centre.
Relapse was defined as evidence of an increase in volume of residual tumour
of greater than 25 % or the presence of metastases, or new onset of positi
ve CSF cytology. Relapse was termed symptomatic if it was diagnosed by test
s performed because of new symptoms that occurred in the interval between s
urveillance examinations. Asymptomatic relapse was diagnosed solely on the
basis of surveillance imaging. Survival time to relapse was calculated from
the date of the first surgical procedure.
Results. Surveillance imaging detected 17 (71%) of the 24 relapses that occ
urred later than 6 months after diagnosis. All seven patients who presented
with symptoms between scans have died, with a median survival from relapse
of 5 months. Median survival from relapse in the patients detected by surv
eillance was 44 months, and four remain alive at 44-75 months. The patients
detected by surveillance tended to have less advanced disease, which was m
ore amenable to salvage therapy.
Conclusion. This type of study cannot prove that surveillance imaging impro
ves survival in children with medulloblastoma because of the effects of lea
d time and length biases. Despite this, surveillance does appear to be effe
ctive in detecting potentially curable medulloblastoma relapses and should
be offered to all patients.