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MIB-1
labeling index as a predictor of tumor progression in pilocytic astrocytomas in
children and adolescents
D.
C. Bowers, P. Kapur, N. J. Winick, L. R. Margraf
UT
Southwestern Medcl School, Dallas, TX
Pilocytic
Astrocytomas (PA) are a distinct subtype of low-grade glioma and the most common
CNS tumor of childhood.
The prognostic importance of the MIB-1 Labeling Index (LI) has not been examined
for progression-free survival (PFS) among children with PAs.
Consecutive children from a single institution with a confirmed histologic
diagnosis of PA were examined to identify risk factors for subsequent tumor
progression.
Immunohistochemistry with the MIB-1 antibody was done according to standard
methods.
141 consecutive children with a PA were identified [mean age: 7.6 ±
4.7 years, range: 0.43 - 18.56 years; 78 (55.3%) males].
After a mean follow-up period of 4.45 years, 53 patients have experienced tumor
progression (Kaplan-Meier PFS = 61.25% at 5 years).
The average time from diagnosis to progression was 1.3 ±
1.9 years.
By log rank analysis, PAs with an MIB-1 LI of ³
2.0 had a shortened PFS compared to PAs with a MIB-1 LI < 2.0 (p value =
0.035).
PAs that had complete tumor resections, located in the cerebellum, treated with
surgery only had a more prolonged PFS compared to tumors that had incomplete
tumor resections, were located elsewhere, and received adjuvant therapy (all p
values = 0.001).
Tumors located in the optic pathways had a shorter PFS than located elsewhere (p
value = 0.001).
Age at diagnosis and tumors located elsewhere in the brain were not associated
with PFS.
By Cox regression multivariate analysis, tumors that were completely resected
were less likely to progress than incompletely resected tumors (p = 0.001), and
tumors located in the cerebellum were less likely to progress than tumors
located in other locations (p = 0.019).
Despite a reputation as a benign tumor, over one third of PAs in children
progress.
An MIB-1 LI of ³
2.0 was associated with an increased frequency of tumor progression.
PAs that are completely resected, and are located in the cerebellum have the
best prognosis.
Further work remains to better understand the biology of this relatively common
neoplasm, and how it influences clinical progression.
© Copyright 2003
American Society of Clinical Oncology All rights
reserved worldwide
Source: http://www.asco.org/ac/1,1003,_12-002489-00_18-002003-00_19-00104528-00_29-00A,00.asp?cat=CNS+Tumors&parent=
Central+Nervous+System+Tumors&returnpid=2325&SubCat_ID=4
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