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Estrogen receptor status confers a distinct pattern of response to neoadjuvant chemotherapy: implications for optimal durations of therapy Distinct patterns of response according to ER expression

Cited 10 time in Web of Science Cited 10 time in Scopus
Authors

Moon, Hyeong-Gon; Im, Seock-Ah; Han, Wonshik; Oh, Do-Youn; Han, Sae-Won; Keam, Bhumsuk; Park, In Ae; Chang, Jung Min; Moon, Woo Kyung; Cho, Nariya; Noh, Dong-Young

Issue Date
2012-08
Publisher
Kluwer Academic Publishers
Citation
Breast Cancer Research and Treatment, Vol.134 No.3, pp.1133-1140
Abstract
Estrogen receptor (ER) expression status is an independent factor predicting response to neoadjuvant systemic treatment (NST). In the current study, we aimed to investigate the characteristics of NST response and benefits of extended NST cycles according to ER expression status. We investigated the outcomes of different durations of anthracycline-taxane-based NST in 377 operable breast cancer patients treated between Aug 2008 and June 2011. In 89 patients, the serial radiologic tumor response was assessed with either ultrasonography or computed tomography. Ninety-six patients (25.5 %) received extended cycles of anthracycline-taxane-based NST (6-8 cycles) and 281 patients (74.5 %) received 3-4 cycles of NST. Treatment with extended cycles of NST led to a significant increase in the pCR rate in ER-positive tumors only (2.1-11.7 %, p = 0.008 for ER-positive tumors and 20.0-19.4 %, p = 0.941 for ER-negative tumors). Serial assessment of radiologic tumor size during extended NST therapy revealed continuous shrinkage of ER-positive tumors during the chemotherapy cycles, while ER-negative tumors mainly achieved size reduction during the first 3-4 cycles with no significant additional tumor shrinkage during the extended cycles of NST. In this study, we report a distinct pattern of response to NST according to ER expression status in breast cancer. Our observation generates the hypothesis that the optimal duration of NST can be tailored to the molecular phenotypes of tumors.
ISSN
0167-6806
URI
https://hdl.handle.net/10371/177172
DOI
https://doi.org/10.1007/s10549-012-2145-y
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  • College of Medicine
  • Department of Medicine
Research Area Clinical Medicine

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