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DOI 10.4103/0973-1482.163851

Медицинская библиотека · Journal of cancer research and therapeutics · 2015

Clinicopathological features of invasive lobular carcinoma of the breast: A nationwide multicenter study in China.

Zhu M Z, Yu X F, He X M, Feng W L, Fan J H, Li J, Xu F, Tang Z H, Zhang B N, Qiao Y L, Zheng S, Yang H J

СтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

To analyze the clinicopathological features of invasive lobular carcinoma (ILC) and compare them with invasive ductal carcinoma (IDC), hoping to find the fact of ILC in China and assist the decision makers with proper individualized treatment.

MATERIALS AND

METHODS

A nationwide multicenter retrospective study was performed. A total of 4211 primary breast cancer cases were randomly selected from 1999 to 2008 in seven regions of China. ILC cases were compared with IDC by clinicopathological features and molecular subtypes.

RESULTS

A total of 135 (3.2%) ILC and 3471 (82.4%) IDC cases were included for analysis. The age, tumor size, menopausal state, family history, nodal status, and stage of ILC were similar to that of IDC. ILC was more likely to be positive for estrogen receptor (65.5% vs. 57.7%) and progesterone receptor (64.7% vs. 58.5%), and less likely to overexpress human epidermal growth factor receptor-2 (17.3% vs. 23.6%). Even though, these differences are not significant, the proportion of luminal A type of ILC is significantly larger than that of IDC (54.8% vs. 42.7%; P < 0.05).

CONCLUSION

ILC has a larger proportion of luminal A type compared with IDC. Larger sample size study for better known of molecular subtypes of ILC is needed in future to individualize the treatment decision.

Для цитирования: Zhu M Z, Yu X F, He X M, Feng W L, Fan J H, Li J, Xu F, Tang Z H, Zhang B N, Qiao Y L, Zheng S, Yang H J. Clinicopathological features of invasive lobular carcinoma of the breast: A nationwide multicenter study in China.. Journal of cancer research and therapeutics. 2015. DOI: 10.4103/0973-1482.163851.

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