Assessment of dual-probe Her-2 fluorescent in situ hybridization in breast cancer by the 2013 ASCO/CAP guidelines produces more equivocal results than that by the 2007 ASCO/CAP guidelines.
Assessment of dual-probe Her-2 fluorescent in situ hybridization in breast cancer by the 2013 ASCO/CAP guidelines produces more equivocal results than that by the 2007 ASCO/CAP guidelines.
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2013 年 ASCO/CAP 指南对乳腺癌双探针 Her-2 荧光原位杂交的评估产生的结果比 2007 年 ASCO/CAP 指南更加模棱两可
DOI:
10.1007/s10549-016-3917-6
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发表时间:
2016-08
影响因子:
3.8
通讯作者:
Fu L
中科院分区:
文献类型:
--
作者:
Qian XL;Wen HY;Yang YL;Gu F;Guo XJ;Liu FF;Zhang L;Zhang XM;Fu L
Dual-probe fluorescence in situ hybridization (D-FISH) is a widely accepted method to determine the gene amplification status of human epidermal growth factor receptor 2 (Her-2). In 2013, the American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) updated the guidelines on the Her-2 testing for invasive breast cancer (BCa). The interpretation criteria for D-FISH changed accordingly. In this study, we compared the Her-2 FISH statuses based on the 2013 and 2007 ASCO/CAP guidelines in 1931 cases of BCa with Her-2 D-FISH testing at our hospital. We analyzed the clinicopathologic features of cases with equivocal results by the 2013 ASCO/CAP guidelines. Although the guideline update significantly improved the detection rate of Her-2 amplification, it also significantly increased the rate of equivocal results, posing a dilemma for clinical management. The equivocal results had a good reproducibility. The distribution of D-FISH-equivocal cases did not correlate with Her-2 status by immunohistochemistry, suggesting that Her-2 D-FISH equivocality may not reflect Her-2 overexpression. Compared with Her-2-negative cases by D-FISH, Her-2 D-FISH-equivocal cases had higher Ki67 expression, higher histological grade, more frequent lymph node metastasis, and lower estrogen receptor α expression, indicating a group of BCa with worse prognosis. The clinical significance of Her-2-equivocal results by D-FISH warrants further investigation.
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影响因子:
6.4
作者:
Bethune, Gillian C.;van Zanten, Daniel Veldhuijzen;Barnes, Penny J.
通讯作者:
Barnes, Penny J.
影响因子:
2.8
作者:
Pu, Xiaohong;Shi, Jiong;Ye, Qing
通讯作者:
Ye, Qing
影响因子:
5.8
作者:
Sapino, Anna;Maletta, Francesca;Marchio, Caterina
通讯作者:
Marchio, Caterina
DOI:
10.1093/jnci/95.2.142
发表时间:
2003-01-15
期刊:
JOURNAL OF THE NATIONAL CANCER INSTITUTE
影响因子:
--
作者:
Konecny, G;Pauletti, G;Slamon, DJ
通讯作者:
Slamon, DJ
影响因子:
45.3
作者:
Hammond, M. Elizabeth H.;Hayes, Daniel F.;Wolff, Antonio C.
通讯作者:
Wolff, Antonio C.