EXPRESSION OF P-GLYCOPROTEIN IN HIGH-GRADE OSTEOSARCOMAS IN RELATION TO CLINICAL OUTCOME

被引:350
作者
BALDINI, N
SCOTLANDI, K
BARBANTIBRODANO, G
MANARA, MC
MAURICI, D
BACCI, G
BERTONI, F
PICCI, P
SOTTILI, S
CAMPANACCI, M
SERRA, M
机构
[1] Dipartimento di Oncologia, Istituti Ortopedici Rizzoli, Bologna
关键词
D O I
10.1056/NEJM199511233332103
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1380 / 1385
页数:6
相关论文
共 53 条
[1]  
BACCI G, 1993, CANCER, V72, P3227, DOI 10.1002/1097-0142(19931201)72:11<3227::AID-CNCR2820721116>3.0.CO
[2]  
2-C
[3]  
BALDINI N, IN PRESS EUR J CELL
[4]  
Blaney S M, 1993, Cancer Treat Res, V62, P55
[5]   MECHANISM OF MULTIDRUG RESISTANCE IN HUMAN TUMOR-CELL LINES AND COMPLETE REVERSION OF CELLULAR-RESISTANCE [J].
BOIOCCHI, M ;
TOFFOLI, G .
EUROPEAN JOURNAL OF CANCER, 1992, 28A (6-7) :1099-1105
[6]   P-GLYCOPROTEIN, MULTIDRUG-RESISTANCE AND TUMOR PROGRESSION [J].
BRADLEY, G ;
LING, V .
CANCER AND METASTASIS REVIEWS, 1994, 13 (02) :223-233
[7]   MECHANISM OF MULTIDRUG RESISTANCE [J].
BRADLEY, G ;
JURANKA, PF ;
LING, V .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 948 (01) :87-128
[8]  
CAMPANACCI M, 1981, CANCER, V48, P1569, DOI 10.1002/1097-0142(19811001)48:7<1569::AID-CNCR2820480717>3.0.CO
[9]  
2-X
[10]   IMMUNOHISTOCHEMICAL DETECTION OF P-GLYCOPROTEIN - PROGNOSTIC CORRELATION IN SOFT-TISSUE SARCOMA OF CHILDHOOD [J].
CHAN, HSL ;
THORNER, PS ;
HADDAD, G ;
LING, V .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (04) :689-704