Literature DB >> 27885439

Weekly paclitaxel plus carboplatin with or without trastuzumab as neoadjuvant chemotherapy for HER2-positive breast cancer: loss of HER2 amplification and its impact on response and prognosis.

Ruo-Xi Wang1,2, Sheng Chen3,4, Xi Jin1,2, Can-Ming Chen1,2, Zhi-Ming Shao5,6,7.   

Abstract

PURPOSE: Neoadjuvant chemotherapy (NCT) plus anti-HER2 agents are the standard of care for locally advanced HER2-positive breast cancer. The aim of this study was to evaluate the prevalence and prognostic impact of HER2 loss in patients with HER2-positive disease treated with neoadjuvant therapy with or without trastuzumab.
METHODS: 549 consecutive HER2-positive patients were included in this study. 379 patients were treated with paclitaxel, carboplatin, and trastuzumab (PCH cohort) and 170 were treated with paclitaxel and carboplatin only (PC cohort). Conversion of biomarkers before and after NCT was evaluated via immunohistochemistry (IHC) test. Cox regression model was used to investigate prognostic markers to relapse-free survival (RFS).
RESULTS: 50.9% patients were considered as pCR responder in PCH cohort, whereas only 25.9% of patients experienced pCR in PC cohort (P < 0.001). HER2 loss were more frequently shown in PCH cohort with a proportion of 19.8%, compared to 9.4% in PC cohort (P = 0.009). In PCH cohort, patients with a loss of HER2 expression tended to have a higher risk of relapse compared to patients with maintained HER2 expression (HR = 2.639, 95% CI 1.103-6.311, P = 0.029). However, it did not correlate to patient outcome in the PC cohort (P = 0.296). Loss of HER2 was also correlated to ER conversion in PCH cohort.
CONCLUSION: Our study has provided new evidence that anti-HER2 treatment has a significant impact on HER2 loss. Far more importantly, the loss of HER2 amplification could identify non-pCR patients with high risk of disease relapse, which might help in tailoring following systemic treatment.

Entities:  

Keywords:  Breast cancer; HER2-positive; Neoadjuvant chemotherapy; Pathological complete response; Trastuzumab

Mesh:

Substances:

Year:  2016        PMID: 27885439     DOI: 10.1007/s10549-016-4064-9

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  4 in total

1.  YES1 activation induces acquired resistance to neratinib in HER2-amplified breast and lung cancers.

Authors:  Tatsuaki Takeda; Hiromasa Yamamoto; Ken Suzawa; Shuta Tomida; Shunsaku Miyauchi; Kota Araki; Kentaro Nakata; Akihiro Miura; Kei Namba; Kazuhiko Shien; Junichi Soh; Tadahiko Shien; Yoshihisa Kitamura; Toshiaki Sendo; Shinichi Toyooka
Journal:  Cancer Sci       Date:  2020-01-16       Impact factor: 6.716

2.  Efficacy and safety of neoadjuvant therapy for HER2-positive early breast cancer: a network meta-analysis.

Authors:  Jie Zhang; Yushuai Yu; Yuxiang Lin; Shaohong Kang; Xinyin Lv; Yushan Liu; Jielong Lin; Jun Wang; Chuangui Song
Journal:  Ther Adv Med Oncol       Date:  2021-04-03       Impact factor: 8.168

3.  Optimal Duration of Neoadjuvant Taxane and Carboplatin Combined With Anti-HER2 Targeted Therapy for HER2-Positive Breast Cancer.

Authors:  Yifan Xie; Siyu Wu; Ying Zhang; Jianwei Li; Miao Mo; Zhimin Shao; Guangyu Liu
Journal:  Front Oncol       Date:  2021-06-08       Impact factor: 6.244

4.  Efficacy of Neoadjuvant Chemotherapy with Epirubicin and Cyclophosphamide and Weekly Paclitaxel and Trastuzumab in Human Epidermal Growth Factor Receptor 2-Positive Breast Carcinoma: A Real-World Study.

Authors:  Mengmeng Zhang; Ling Li; Shiyong Zhang; Wenlong Zhu; Senguo Yang; Guangsheng Di; Xiaoxia Ma; Haisong Yang
Journal:  Biomed Res Int       Date:  2020-05-02       Impact factor: 3.411

  4 in total

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