INTERPHASE CYTOGENETIC (IN-SITU HYBRIDIZATION) ANALYSIS OF ASTROCYTOMAS USING ARCHIVAL, FORMALIN-FIXED, PARAFFIN-EMBEDDED TISSUE AND NONFLUORESCENT LIGHT-MICROSCOPY
A. Perry et al., INTERPHASE CYTOGENETIC (IN-SITU HYBRIDIZATION) ANALYSIS OF ASTROCYTOMAS USING ARCHIVAL, FORMALIN-FIXED, PARAFFIN-EMBEDDED TISSUE AND NONFLUORESCENT LIGHT-MICROSCOPY, American journal of clinical pathology, 108(2), 1997, pp. 166-174
Astrocytomas contain nonrandom chromosomal abnormalities that recently
have been correlated with shortened patient survival. Two frequently
reported aberrations are trisomy 7 and monosomy 10. We assessed the nu
merical complement of chromosomes 7 and 10 in formalin-fixed, paraffin
-embedded brain biopsy tissue from 28 diffuse astrocytomas by in situ
hybridization using a nonfluorescent enzymatic detection system. Clini
cal follow-up of at least 5 years was available in 26 cases (93%). Mon
osomy 10 was identified in 7 cases (25%): astrocytoma, 1 case; anaplas
tic astrocytoma, 1 case; and glioblastoma, 5 cases. Trisomy 7 was iden
tified in 11 cases (39%): astrocytoma, 5 cases; glioblastoma, 6 cases.
Multivariate analysis revealed that monosomy 10 was the most statisti
cally significant negative predictor of patient survival. Numerical ch
romosomal abnormalities ale detectable in astrocytomas in archival tis
sue using interphase cytogenetics and nonfluorescent light microscopy.
Although larger studies are required, our data suggest that potential
ly useful prognostic information may be obtained with this approach.