Prognostic significance of Ki67 in Chinese women diagnosed with ER + /HER2 - breast cancers by the 2015 St. Gallen consensus classification
This study evaluated the distribution pattern of the Ki67-labeling index (LI) among patients at a Chinese breast cancer center, and analyzed its prognostic significance in the 2015 St Gallen consensus breast cancer classification, estrogen receptor-positive and human epidermal growth factor receptor...
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Veröffentlicht in: | BMC cancer 2017-01, Vol.17 (1), p.28-28, Article 28 |
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Zusammenfassung: | This study evaluated the distribution pattern of the Ki67-labeling index (LI) among patients at a Chinese breast cancer center, and analyzed its prognostic significance in the 2015 St Gallen consensus breast cancer classification, estrogen receptor-positive and human epidermal growth factor receptor 2-negative(ER
/HER2
)subtype.
We classified 939 women with ER
/HER2
breast cancer into three groups by Ki67-LI levels, and followed their clinicopathologic characteristics and prognoses.
In the 939 eligible subjects, 342 had Ki67-LI ≤10% (Ki67
), 281 had Ki67-LI between 10 and 30% (Ki67
), and 316 had Ki67-LI ≥30% (Ki67
). Although the Ki67
group had less favorable clinicopathologic factors, the Ki67
group's factors varied considerably. Kaplan-Meier estimates showed that disease-free survival(DFS) for the Ki67
group was significantly shorter than the Ki67
group but longer than the Ki67
group. Ki67-LI had independent prognostic significance in multivariate analysis. Other diagnostic factors, including tumor size >2 cm, positive lymph nodes, and grade III disease, were significantly associated with poorer disease-free survival only in the Ki67
group.
For patients with ER
/HER2
breast cancer, we confirmed three distinct risk patterns by Ki67-LI levels according to the 2015 St Gallen consensus. For patients with clearly low or high Ki67-LI, straightforward clinical decisions could be offered, but for patients with intermediate Ki67-LI, other factors might provide valuable information. |
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ISSN: | 1471-2407 1471-2407 |
DOI: | 10.1186/s12885-016-3021-7 |