Effect of mutated TP53 on response of advanced breast cancers to high-dose chemotherapy

被引:135
作者
Bertheau, P
Plassa, F
Espié, M
Turpin, E
de Roquancourt, A
Marty, M
Lerebours, F
Beuzard, Y
Janin, A
de Thé, H
机构
[1] Hop St Louis, Serv Biochim B, F-75475 Paris 10, France
[2] Hop St Louis, CNRS, UPR 9051, F-75475 Paris, France
[3] Hop St Louis, INSERM, ERM 0220, F-75475 Paris 10, France
[4] Hop St Louis, Serv Pathol, F-75475 Paris 10, France
[5] Hop St Louis, Serv Oncol, F-75475 Paris 10, France
关键词
D O I
10.1016/S0140-6736(02)09969-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
TP53 activation by genotoxic drugs can induce apoptosis or cell-cycle arrest. Thus, whether the gene is mutated or wild type could affect the response of a tumour to chemotherapy. Clinical data are unclear, possibly as a result of heterogeneity of tumours, drugs, methods of assessing response, or TP53 status. We studied 50 non-inflammatory, locally advanced breast cancers that had been treated with high doses of a combination of epirubicin and cyclophosphamide. We noted eight complete responses, which all occurred in the 14 patients with tumours containing mutated TP53 (p<0.0001). In high-grade, advanced breast cancers, inactivation of the TP53 pathway could greatly improve the response to this chemotherapy regimen.
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收藏
页码:852 / 854
页数:3
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