Over the last years, distinct genetic lesions have been associated with ind
ividual tumor entities. Stereotactic biopsy has become an essential diagnos
tic tool in surgical neuro-oncology. In order to evaluate the potential of
molecular analyses in stereotactic biopsies, we examined a series of 156 hu
man brain tumors from patients undergoing stereotactic biopsy for molecular
alterations typically seen in astrocytic gliomas and compared those result
s with a control group of 268 astrocytic tumors obtained at open surgery. S
tereotactic biopsies of astrocytomas with borderline histopathological feat
ures between the WHO grades II and III showed a higher rate of allelic loss
es on chromosome 10 than these of the WHO grade II from open surgery (p = 0
.011). Stereotactic biopsies of astrocytomas with borderline histopathologi
cal, features between the WHO grades III and IV showed a higher rate of all
elic losses on chromosome IO than those of the WHO grade III from open surg
ery (p = 0.013). This indicates that stereotactic biopsies with features in
termediate between grades are likely to correspond to the higher malignancy
grade. Our data demonstrate that molecular genetic approaches can be succe
ssfully applied to stereotactic glioma biopsies. The difference in the dist
ribution of malignancy associated genetic alterations between a stereotacti
c and openly resected group of gliomas indicates that histopathology may un
derestimate the malignant potential in some stereotactic specimens. We prop
ose to further evaluate the molecular analysis of stereotactic glioma biops
ies as a useful adjunct to standard histopathological procedures.