Abstract
Purpose: The identification of a robust IHC marker to predict the response to antiangiogenic bevacizumab in ovarian cancer is of high clinical interest. VEGF-A, the molecular target of bevacizumab, is expressed as multiple isoforms with pro-or antiangiogenic prop-erties, of which VEGF-A165b is the most dominant antiangiogenic isoform. The balance of VEGF-A isoforms is closely related to the angiogenic capacity of a tumor and may define its vulnerability to antiangiogenic therapy. We investigated whether the expression of VEGF-A165b could be related to the effect of bevacizumab in advanced ovarian cancer patients.Experimental Design: Formalin-fixed paraffin-embedded tis-sues from 413 patients of the ICON7 multicenter phase III trial, treated with standard platinum-based chemotherapy with or with-out bevacizumab, were probed for VEGF-A165b expression by IHC. Results: In patients with low VEGF-A165b expression, the addi-tion of bevacizumab to standard platinum-based chemotherapy significantly improved progression-free (HR: 0.727;95% CI, 0.538- 0.984;P 1/4 0.039) and overall survival (HR: 0.662;95% CI, 0.458- 0.958;P 1/4 0.029). Multivariate analysis showed that the addition of bevacizumab in low VEGF-A165b-expressing patients conferred significant improvements in progression-free survival (HR: 0.610;95% CI, 0.446-0.834;P 1/4 0.002) and overall survival (HR: 0.527;95% CI, 0.359-0.775;P 1/4 0.001), independently from established risk factors.Conclusions: We demonstrate for the first time that bevaci-zumab may differentially improve the prognosis of advanced ovarian cancer patients with low expression of VEGF-A165b, an antiangiogenic VEGF-A splice variant. We envision that this novel biomarker could be implemented into routine diag-nostics and may have direct clinical implications for guiding bevacizumab-related treatment decisions in advanced ovarian cancer patients.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Medizin |
Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
ISSN: | 1078-0432 |
Sprache: | Englisch |
Dokumenten ID: | 113601 |
Datum der Veröffentlichung auf Open Access LMU: | 02. Apr. 2024, 07:53 |
Letzte Änderungen: | 02. Apr. 2024, 07:53 |