Adjuvant Capecitabine for Breast Cancer after Preoperative Chemotherapy

Patients who complete neoadjuvant chemotherapy for breast cancer without a pathological complete response have a high risk of relapse. A randomized trial comparing capecitabine with no additional adjuvant therapy showed that capecitabine prolonged disease-free and overall survival. Patients who have...

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Published inThe New England journal of medicine Vol. 376; no. 22; pp. 2147 - 2159
Main Authors Masuda, Norikazu, Lee, Soo-Jung, Ohtani, Shoichiro, Im, Young-Hyuck, Lee, Eun-Sook, Yokota, Isao, Kuroi, Katsumasa, Im, Seock-Ah, Park, Byeong-Woo, Kim, Sung-Bae, Yanagita, Yasuhiro, Ohno, Shinji, Takao, Shintaro, Aogi, Kenjiro, Iwata, Hiroji, Jeong, Joon, Kim, Aeree, Park, Kyong-Hwa, Sasano, Hironobu, Ohashi, Yasuo, Toi, Masakazu
Format Journal Article
LanguageEnglish
Published United States Massachusetts Medical Society 01.06.2017
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Summary:Patients who complete neoadjuvant chemotherapy for breast cancer without a pathological complete response have a high risk of relapse. A randomized trial comparing capecitabine with no additional adjuvant therapy showed that capecitabine prolonged disease-free and overall survival. Patients who have residual invasive breast cancer after the receipt of neoadjuvant chemotherapy have a high risk of relapse. 1 The rate of complete response as assessed on pathological testing (hereafter, pathological complete response) ranges from 13 to 22% among patients with human epidermal growth factor receptor 2 (HER2)–negative primary breast cancer. 1 Patients who do not have a pathological complete response after the receipt of neoadjuvant taxane and anthracycline chemotherapy have a 20 to 30% risk of relapse. 2 Patients with HER2-negative cancer who receive neoadjuvant chemotherapy often receive postoperative radiation therapy, whereas endocrine therapy is administered to patients with hormone-receptor–positive disease . . .
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ISSN:0028-4793
1533-4406
DOI:10.1056/NEJMoa1612645