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. Author manuscript; available in PMC: 2013 Aug 1.
Published in final edited form as: Am J Surg Pathol. 2012 Aug;36(8):1186–1193. doi: 10.1097/PAS.0b013e3182518e12

Table 3. Multivariate analyses.

Modeling according to clinical factors significant on univariate analysis showed that low-to-moderate EGFR amplification was an independent adverse prognostic factor for overall survival, both in all cases with known adjuvant therapy status (upper) and the subset treated with TMZ (lower). HR = hazard ratio, CI = confidence interval, EGFR = epidermal growth factor receptor; CEP7 = centromeric enumeration probe for chromosome 7, TMZ = temozolomide.

All cases with known adjuvant therapy status (N = 465)
Variable HR 95% CI P
Patient age > 45 years versus ≤ 45 years 2.46 1.79-3.38 < 0.0001
Resection versus biopsy 0.42 0.34-0.52 < 0.0001
TMZ versus no TMZ 0.39 0.30-0.46 < 0.0001
EGFR:CEP7 ratio = 2-20 versus non-amplified or ratio > 20 1.42 1.07-1.89 0.017
Only cases treated with TMZ (N = 312)
Variable HR 95% CI P
Patient age > 45 years versus ≤ 45 years 2.09 1.41-3.09 0.0002
Resection versus biopsy 0.39 0.29-0.51 < 0.0001
EGFR: CEP7 ratio = 2-20 versus non-amplified or ratio > 20 1.56 1.10-2.22 0.013