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dc.contributor.author | Redondo, Maximino | es_ES |
dc.contributor.author | Funez, Rafael | es_ES |
dc.contributor.author | Medina-Cano, Francisco | es_ES |
dc.contributor.author | Rodrigo, Isabel | es_ES |
dc.contributor.author | Acebal, Mercedes | es_ES |
dc.contributor.author | Tellez, Teresa | es_ES |
dc.contributor.author | Roldan, M. Jose | es_ES |
dc.contributor.author | Hortas, M. Luisa | es_ES |
dc.contributor.author | Bellinvia, Ana | es_ES |
dc.contributor.author | Pereda, Teresa | es_ES |
dc.contributor.author | Domingo, Laia | es_ES |
dc.contributor.author | Morales Suárez-Varela, María M. | es_ES |
dc.contributor.author | Sala, Maria | es_ES |
dc.contributor.author | Rueda, Antonio | es_ES |
dc.date.accessioned | 2015-06-19T10:19:54Z | |
dc.date.available | 2015-06-19T10:19:54Z | |
dc.date.issued | 2012 | es_ES |
dc.identifier.citation | BMC Cancer Vol. 12 pp. 604-604 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10550/44557 | |
dc.description.abstract | BackgroundThe aim of this study was to measure the biological characteristics involved in tumorigenesis and the progression of breast cancer in symptomatic and screen-detected carcinomas to identify possible differences.MethodsFor this purpose, we evaluated clinical-pathological parameters and proliferative and apoptotic activities in a series of 130 symptomatic and 161 screen-detected tumors.ResultsAfter adjustment for the smaller size of the screen-detected carcinomas compared with symptomatic cancers, those detected in the screening program presented longer disease-free survival (RR = 0.43, CI = 0.19-0.96) and had high estrogen and progesterone receptor concentrations more often than did symptomatic cancers (OR = 3.38, CI = 1.72-6.63 and OR = 3.44, CI = 1.94-6.10, respectively). Furthermore, the expression of bcl-2, a marker of good prognosis in breast cancer, was higher and HER2/neu expression was lower in screen-detected cancers than in symptomatic cancers (OR = 1.77, CI = 1.01-3.23 and OR = 0.64, CI = 0.40-0.98, respectively). However, when comparing prevalent vs incident screen-detected carcinomas, prevalent tumors were larger (OR = 2.84, CI = 1.05-7.69), were less likely to be HER2/neu positive (OR = 0.22, CI = 0.08-0.61) and presented lower Ki67 expression (OR = 0.36, CI = 0.17-0.77). In addition, incident tumors presented a shorter survival time than did prevalent ones (RR = 4.88, CI = 1.12-21.19).ConclusionsIncident carcinomas include a variety of screen-detected carcinomas that exhibit differences in biology and prognosis relative to prevalent carcinomas. The detection method is important and should be taken into account when making therapy decisions. | es_ES |
dc.subject | Breast cancer | es_ES |
dc.subject | Detection methods | es_ES |
dc.subject | Proliferation | es_ES |
dc.subject | Apoptosis | es_ES |
dc.subject | Survival | es_ES |
dc.title | Detection methods predict differences in biology and survival in breast cancer patients | es_ES |
dc.type | journal article | es_ES |
dc.identifier.doi | 10.1186/1471-2407-12-604 | es_ES |
dc.identifier.idgrec | 084751 | es_ES |