Jn. Scott et al., LONG-TERM GLIOBLASTOMA-MULTIFORME SURVIVORS - A POPULATION-BASED STUDY, Canadian journal of neurological sciences, 25(3), 1998, pp. 197-201
Background: Long-term glioblastoma multiforme survivors (LTGBMS) are u
ncommon. The frequency which these occur in an unselected population a
nd factors which produce these unusually long survivors are unknown. O
bjectives: To determine in a population-based study 1) the frequency o
f LTGBMS in a population and 2) identify which patient, treatment or t
umor characteristics would predict which glioblastoma (GBM) patient wo
uld become a LTGBMS, Methods: The Alberta Cancer Registry was used to
identify all patients diagnosed with GEM in southern Alberta between 1
/1/75 - 12/31/91, Patient charts were reviewed and histology re-examin
ed by a blinded neuropathologist, LTGBMS were defined as (GBM patients
surviving greater than or equal to 3 years after diagnosis. Each LTGB
MS was compared to three age-, gender-, and year of diagnosis-matched
controls to compare patient, treatment, and tumor factors to GEM patie
nts without long-term survival. Results: There were 279 GBMs diagnosed
in the study period. Five (1.8%) survived greater than or equal to th
ree years (range, 3.2-15.8 years). Seven additional long-term survivor
s, who carried a diagnosis of GEM, were excluded after neuropathologic
review; the most common revised diagnosis was malignant oligodendrogl
ioma, LTGBMS (avg,age = 45 years) were significantly younger when comp
ared to all GEM patients (avg. age = 59 years, p = 0.0001) diagnosed i
n the study period. LTGBMS had a higher KPS at diagnosis (p = 0.001) c
ompared to controls, Tumors from LTGBMS tended to have fewer mitoses a
nd a lower Ki-67 cellular proliferative index compared to controls. Ra
diation-induced dementia was common and disabling in LTGBMS. Conclusio
ns: These data highlight the dismal prognosis for GEM patients who hav
e both a short median survival and very small chance (1.8%) of long-te
rm survival. The LTGBMS were younger, had a higher performance status,
and their tumors tended to proliferate less rapidly than control GEM
patients. When long-term survival does occur it is often accompanied b
y severe treatment-induced dementia.