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1.
Chinese Journal of Pathology ; (12): 140-146, 2005.
Article Dans Chinois | WPRIM | ID: wpr-265169

Résumé

<p><b>OBJECTIVE</b>To evaluate the clinical value of HER2 overexpression in breast cancer and its prognostic implication in patients with lymph node negative breast carcinoma.</p><p><b>METHODS</b>The following electronic database were extracted using appropriate inclusive and exclusive standards: Cochrane library, PUBMED, Embase (1984 - 2003), OVID, CMCC and CNKI. Excel and RevMan 4.2 were used for statistical analysis.</p><p><b>RESULTS</b>Fifty-six articles were extracted to calculate the positive rate of HER2 overexpression. The pooled positive rate was 23.14% [19.54%, 26.73%], with positive immunohistochemistry (IHC) rate of 23.13% [19.49%, 26.77%] and positive FISH rate of 20.90% [15.54%, 26.25%]. Seven articles were used to evaluate prognostic predication of HER2 expression. It was concluded that in patients with lymph node negative breast carcinoma, HER2 overexpression (both IHC and FISH) independently predicted a poor prognosis based on disease-free survival (DFS) and overall survival (OS) with a P < 0.05. For DFS, the pooled RR was 1.38 [1.07, 1.80] with 1.16 [1.02, 1.31] for IHC and 1.98 [1.56, 2.52] for FISH. For OS, the pooled RR was 1.58 [1.16, 2.14] with 1.37 [1.14 to 1.64] for IHC and 2.33 [1.45 to 3.75] for FISH. HER2 overexpression effectively predicted DFS/OS of patients without adjuvant therapy and OS of patients with the therapy, but not for DFS, with the pooled RR of 1.46 [1.02, 2.09] and 1.11 [0.95, 1.31] for DFS, respectively and the pooled RR of 1.93 [1.44 to 2.58] and 1.25 [1.01, 1.56] for OS, respectively.</p><p><b>CONCLUSIONS</b>In patients with lymph node negative breast carcinoma, the positive rate of HER2 overexpression is 23.14%. HER2 overexpression indicates a poor prognosis and adjuvant therapy after surgery should be recommended.</p>


Sujets)
Femelle , Humains , Tumeurs du sein , Génétique , Métabolisme , Anatomopathologie , Thérapeutique , Traitement médicamenteux adjuvant , Survie sans rechute , Gènes erbB-2 , Noeuds lymphatiques , Anatomopathologie , Mastectomie , Pronostic , Récepteur ErbB-2 , Métabolisme , Taux de survie
2.
Chinese Journal of Pathology ; (12): 316-319, 2004.
Article Dans Chinois | WPRIM | ID: wpr-283517

Résumé

<p><b>OBJECTIVE</b>To evaluate the expression of cytokeratins in intraductal proliferative lesions of breast, including usual ductal hyperplasia (UDH), atypical ductal hyperplasia (ADH), ductal carcinoma-in-situ (DCIS) and its role in differential diagnosis.</p><p><b>METHODS</b>Ninety two cases of paraffin-embedded lesional breast tissue, 30 cases of frozen samples, cell cultures of hyperplastic ductal cells and 2 invasive ductal carcinoma cell lines (T47D and MCF-7) were used for this study. Immunohistochemistry was performed using EnVision method for 34betaE12, CK8 and CK14.</p><p><b>RESULTS</b>The percentage of 34betaE12-positivity in paraffin-embedded samples of UDH, ADH, DCIS and invasive ductal carcinoma (IDC) was found to be 95.2%, 33.3%, 19.2% and 12.5% respectively. In frozen tissues, all UDH cases and 55% of IDC cases expressed 34betaE12. The primary UDH cell cultures and T47D cell line were also 34betaE12-positive, whereas MCF7 cell line showed negative staining. The expression rate of CK8 and CK14 in UDH was also different from that in ADH and DCIS.</p><p><b>CONCLUSIONS</b>34betaE12 can be useful in differential diagnosis of intraductal proliferative lesions of the breast. However application of this cytokeratin stain in intraoperative frozen sections is relatively limited. The expression patterns of CK8 and CK14 are also helpful in the differential diagnosis of similar lesions.</p>


Sujets)
Femelle , Humains , Région mammaire , Chimie , Anatomopathologie , Tumeurs du sein , Chimie , Diagnostic , Anatomopathologie , Carcinome canalaire du sein , Chimie , Diagnostic , Anatomopathologie , Carcinome intracanalaire non infiltrant , Chimie , Diagnostic , Lignée cellulaire tumorale , Diagnostic différentiel , Hyperplasie , Kératines , États précancéreux , Chimie , Anatomopathologie
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