Journal of Clinical Oncology, Vol 15, 2858-2865, Copyright © 1997 by American Society of Clinical Oncology
Immunocytochemical markers in stage I lung cancer: relevance to prognosis
U Pastorino, S Andreola, E Tagliabue, F Pezzella, M Incarbone, G Sozzi, M Buyse, S Menard, M Pierotti and F Rilke
Department of Thoracic Surgery, Royal Brompton Hospital, London, United Kingdom. u.pastorino@rbh.nthames.nhs.uk
PURPOSE: This study investigated the frequency of the expression and
prognostic significance of a panel of immunocytochemical markers in
resected non-small-cell lung cancer (NSCLC). PATIENTS AND METHODS: A total
of 515 cases of pathologic stage I NSCLC were analyzed. The median
follow-up time of surviving patients was 102 months. The following
immunocytochemical markers were tested: blood group A and precursors of
blood antigens; laminin receptor; c-erbB1/epidermal growth factor receptor
(EGFR) and c-erbB2/Neu; BCl2; p53; and angiogenesis. Kaplan-Meier estimates
of survival and time to recurrence were calculated for clinical variables
and biologic markers using the Cox model for multivariate analysis.
RESULTS: The pathologic tumor extension (pT) represented the most powerful
prognostic factor for survival (P = .0008) and time to recurrence (P =
.0007). None of the immunocytochemical markers emerged as an independent
predictive factor for survival. Bcl2-positive tumors showed a better time
to recurrence (P = .03), but the difference lost statistical significance
in the multivariate analysis. Of interest, in the group of 137 patients
classified as pT1N0, both EGFR expression and nonangiogenic type of
vascular pattern were associated with a poorer survival (P = .02). However,
data derived from subset analysis must be interpreted cautiously.
CONCLUSION: Our findings do not support a relevant prognostic role of
immunocytochemical markers in NSCLC. The evidence is not sufficient to
alter clinical practice or even to restrict clinical trials of adjuvant
treatments to predefined biologic subsets of patients.
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