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Evaluation of Therapeutic Target Gene Expression Based on Residual Cancer Burden Classification After Neoadjuvant Chemotherapy for HER2-Negative Breast Cancer

Patients with residual disease usually have a poor prognosis after neoadjuvant chemotherapy for breast cancer. The aim of this study was to explore therapeutic targets and potential additional adjuvant treatments for patients with residual disease after standard neoadjuvant chemotherapy. We retrieve...

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Bibliographic Details
Published in:Clinical breast cancer 2020-04, Vol.20 (2), p.117-124.e4
Main Authors: Takahashi, Yuko, Iwamoto, Takayuki, Suzuki, Yoko, Kajiwara, Yukiko, Hatono, Minami, Tsukioki, Takahiro, Kawada, Kengo, Kochi, Mariko, Ikeda, Hirokuni, Shien, Tadahiko, Taira, Naruto, Matsuoka, Junji, Doihara, Hiroyoshi, Toyooka, Shinichi
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Language:English
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Summary:Patients with residual disease usually have a poor prognosis after neoadjuvant chemotherapy for breast cancer. The aim of this study was to explore therapeutic targets and potential additional adjuvant treatments for patients with residual disease after standard neoadjuvant chemotherapy. We retrieved publicly available complementary DNA microarray data from 399 human epidermal growth factor receptor 2 (HER2)-negative primary breast cancer samples from patients who underwent standard neoadjuvant chemotherapy. We analyzed the messenger RNA (mRNA) expression levels of key breast cancer markers and therapeutic target genes according to residual cancer burden (RCB) classification: RCB-0/I, RCB-II, and RCB-III. Among hormone receptor–positive samples, there were more luminal A tumors by PAM50 (Prediction Analysis of Microarray 50 [Prosigna], aka Prosigna Breast Cancer Prognostic Gene Signature Assay) in RCB-III than in RCB-0/I and RCB-II (P 
ISSN:1526-8209
1938-0666
DOI:10.1016/j.clbc.2019.07.001