Expression of P-Glycoprotein in High-Grade Osteosarcomas in Relation to Clinical Outcome

Nicola Baldini(Istituto Ortopedico Rizzoli), Katia Scotlandi(Istituto Ortopedico Rizzoli), Giovanni Barbanti Bròdano(Istituto Ortopedico Rizzoli), Maria Cristina Manara(Istituto Ortopedico Rizzoli), Daniela Maurici(Istituto Ortopedico Rizzoli), Gaetano Bacci(Istituto Ortopedico Rizzoli), Franco Bertoni(Istituto Ortopedico Rizzoli), Piero Picci(Istituto Ortopedico Rizzoli), S. Sottili(Istituto Ortopedico Rizzoli), Mario Campanacci(Istituto Ortopedico Rizzoli), Massimo Serra(Istituto Ortopedico Rizzoli)
New England Journal of Medicine
November 23, 1995
Cited by 399Open Access
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Abstract

BACKGROUND: Increased levels of P-glycoprotein occur in some osteosarcomas. In this study we determined the relation between P-glycoprotein status and outcome in patients with high-grade osteosarcoma. METHODS: P-glycoprotein status was determined immunohistochemically in specimens of osteosarcoma of the extremities (stage II) from 92 patients who were treated with surgery and chemotherapy. The P-glycoprotein status was analyzed in relation to the length of event-free survival. RESULTS: The presence of increased levels of P-glycoprotein in the osteosarcoma was significantly associated with a decreased probability of remaining event-free after diagnosis (P = 0.002). In a multivariate analysis, P-glycoprotein status (P = 0.001) and the extent of tumor necrosis after preoperative chemotherapy (P = 0.04) were independent predictors of clinical outcome. The risk of adverse events was increased substantially (rate ratio, 3.37; 95 percent confidence interval, 1.60 to 7.10) among patients with increased levels of P-glycoprotein in tumor cells, as compared with patients who did not have increased levels of P-glycoprotein in tumor cells. CONCLUSIONS: In patients with high-grade osteosarcoma treated with surgery and chemotherapy, the presence of increased levels of P-glycoprotein in tumor cells is associated with a significantly increased risk of adverse events and is independent of the extent of necrosis after preoperative chemotherapy.


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