文摘
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Summary
To date, chemosensitivity to neoadjuvant chemotherapy of patients with high-grade osteosarcoma is evaluated on surgical resection by evaluation of the percentage of necrotic cells. As yet, no predictive profile of response to chemotherapy has been used in clinical practice. Because we have previously shown that the integrin pathway controls genotoxic-induced cell death and hypoxia, we hypothesized that in primary biopsies, expression of proteins involved in this pathway could be associated with sensitivity to neoadjuvant chemotherapy in high-grade osteosarcoma. We studied ¦Â1, ¦Â3, and ¦Â5 integrin expression and integrin-linked kinase, focal adhesion kinase (FAK), glycogen synthase kinase 3¦Â (GSK3¦Â), Rho B, angiopoietin-2, ¦Â-catenin, and ezrin expression by immunohistochemistry in 36 biopsies of osteosarcomas obtained before treatment. All patients received a chemotherapy regimen in the neoadjuvant setting. An immunoreactive score was assessed, combining the percentage of positive tumor cells and staining intensity. We evaluated the correlation of the biomarkers with response to chemotherapy, metastasis-free survival, and overall survival. A combination of 3 biomarkers (¦Â5 integrin, FAK, and GSK3¦Â) discriminated good and poor responders to chemotherapy, with the highest area under the curve (89.9 % ; 95 % confidence interval, 77.4-1.00) and a diagnostic accuracy of 90.3 % . Moreover, high expression of ezrin was associated with an increased risk of metastasis (hazard ratio, 3.93; 95 % confidence interval, 1.19-12.9; P = .024). We report a protein expression profile in high-grade osteosarcoma associating ¦Â5 integrin, FAK, and GSK3¦Â that significantly correlates with poor response to neoadjuvant chemotherapy. This biomarker profile could help select patients for whom an alternative protocol using inhibitors of this pathway can be proposed.
