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Prognostic impact of clinicopathologic parameters in stage II/III breast cancer treated with neoadjuvant docetaxel and doxorubicin chemotherapy: paradoxical features of the triple negative breast cancer

Bhumsuk Keam1 email, Seock-Ah Im1,6 email, Hee-Jun Kim1 email, Do-Youn Oh1,6 email, Jee Hyun Kim1,6 email, Se-Hoon Lee1,6 email, Eui Kyu Chie2 email, Wonshik Han3 email, Dong-Wan Kim1,6 email, Woo Kyung Moon4 email, Tae-You Kim1,6 email, In Ae Park5 email, Dong-Young Noh3 email, Dae Seog Heo1,6 email, Sung Whan Ha2 email and Yung-Jue Bang1,6 email

1Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea

2Department of Radiation Oncology, Seoul National University College of Medicine, Seoul, Korea

3Department of Surgery, Seoul National University College of Medicine, Seoul, Korea

4Department of Radiology, Seoul National University College of Medicine, Seoul, Korea

5Department of Pathology, Seoul National University College of Medicine, Seoul, Korea

6Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea

author email corresponding author email

BMC Cancer 2007, 7:203doi:10.1186/1471-2407-7-203

Published: 1 November 2007

Abstract

Background

Prognostic factors in locally advanced breast cancer treated with neoadjuvant chemotherapy differ from those of early breast cancer. The purpose of this study was to identify the clinical significance of potential predictive and prognostic factors in breast cancer patients treated by neoadjuvant chemotherapy.

Methods

A total of 145 stage II and III breast cancer patients received neoadjuvant docetaxel/doxorubicin chemotherapy were enrolled in this study. We examined the clinical and biological factors (ER, PR, p53, c-erbB2, bcl-2, and Ki-67) by immunohistochemistry. We analyzed clinical outcome and their correlation with clinicopathologic parameters.

Results

Among the clinicopathologic parameters investigated, none of the marker was correlated with response rate (RR) except triple negative phenotype. Patients with triple negative phenotype showed higher RR (83.0% in triple negative vs. 62.2% in non-triple negative, p = 0.012) and pathologic complete RR (17.0% in triple negative vs. 3.1% in non-triple negative, p = 0.005). However, relapse free survival (RFS) and overall survival (OS) were significantly shorter in triple negative breast cancer patients (p < 0.001, p = 0.021, respectively). Low histologic grade, positive hormone receptors, positive bcl-2 and low level of Ki-67 were associated with prolonged RFS. In addition, positive ER and positive bcl-2 were associated with prolonged OS. In our homogeneous patient population, initial clinical stage reflects RFS and OS more precisely than pathologic stage. In multivariate analysis, initial clinical stage was the only significant independent prognostic factor to impact on OS (hazard ratio 3.597, p = 0.044).

Conclusion

Several molecular markers provided useful predictive and prognostic information in stage II and III breast cancer patients treated with neoadjuvant docetaxel/doxorubicin chemotherapy. Triple negative phenotype was associated with shorter survival, even though it was associated with a higher response rate to neoadjuvant chemotherapy.


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