Literature DB >> 17485900

Does lapatinib, a small-molecule tyrosine kinase inhibitor, constitute a breakthrough in the treatment of breast cancer?

Yoshinori Ito1, Nahomi Tokudome, Tsutomu Sugihara, Shunji Takahashi, Kiyohiko Hatake.   

Abstract

ErbB/HER receptor or its signal transduction pathway is an attractive therapeutic target for breast cancer. Lapatinib, an orally administered dual inhibitor of ErbB1 (EGFR) and ErbB2 (HER2) receptor tyrosine kinases has shown promising results for metastatic breast cancer (MBC). Lapatinib exhibited activity against trastuzumab-refractory MBC and showed an acceptable adverse event profile such as transient mild rash, diarrhea and nausea. The addition of lapatinib to capecitabine resulted in significantly prolonged time to progression. Large randomized trials using lapatinib following chemotherapy and surgery are ongoing for early stage HER2-overexpressing breast cancer. Various combinations with agents such as paclitaxel, aromatase inhibitors, or other molecular targeted agents are currently being investigated in clinical trials. If these approaches overcome the limitations of trastuzumab, lapatinib will become an effective treatment option for breast cancer in the near future.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17485900     DOI: 10.2325/jbcs.971

Source DB:  PubMed          Journal:  Breast Cancer        ISSN: 1340-6868            Impact factor:   4.239


  12 in total

Review 1.  Lapatinib.

Authors:  Sohita Dhillon; Antona J Wagstaff
Journal:  Drugs       Date:  2007       Impact factor: 9.546

2.  Monitoring circulating epithelial tumour cells (CETC) to gauge therapy: in patients with disease progression after trastuzumab persisting CETC can be eliminated by combined lapatinib treatment.

Authors:  Oumar Camara; Cornelia Jörke; Ulrike Hammer; Anne Egbe; Carola Rabenstein; Ingo B Runnebaum; Klaus Hoeffken; Katharina Pachmann
Journal:  J Cancer Res Clin Oncol       Date:  2008-10-21       Impact factor: 4.553

Review 3.  Lapatinib: a review of its use in the treatment of HER2-overexpressing, trastuzumab-refractory, advanced or metastatic breast cancer.

Authors:  James E Frampton
Journal:  Drugs       Date:  2009-10-22       Impact factor: 9.546

4.  Candidate biomarker assessment for pharmacological response.

Authors:  William C Reinhold; Fathi Elloumi; Sudhir Varma; Jacques Robert; Gordon B Mills; Yves Pommier
Journal:  Transl Oncol       Date:  2020-07-08       Impact factor: 4.243

5.  Targeting the tumor microenvironment: focus on angiogenesis.

Authors:  Fengjuan Fan; Alexander Schimming; Dirk Jaeger; Klaus Podar
Journal:  J Oncol       Date:  2011-08-24       Impact factor: 4.375

6.  Lapatinib induces autophagy, apoptosis and megakaryocytic differentiation in chronic myelogenous leukemia K562 cells.

Authors:  Huey-Lan Huang; Yu-Chieh Chen; Yu-Chuen Huang; Kai-Chien Yang; Hsin yi Pan; Shou-Ping Shih; Yu-Jen Chen
Journal:  PLoS One       Date:  2011-12-22       Impact factor: 3.240

7.  Lapatinib induces autophagic cell death and differentiation in acute myeloblastic leukemia.

Authors:  Yu-Jen Chen; Li-Wen Fang; Wen-Chi Su; Wen-Yi Hsu; Kai-Chien Yang; Huey-Lan Huang
Journal:  Onco Targets Ther       Date:  2016-07-20       Impact factor: 4.147

8.  Clinical activities of the epidermal growth factor receptor family inhibitors in breast cancer.

Authors:  Elizabeth S Henson; James B Johnston; Marek Los; Spencer B Gibson
Journal:  Biologics       Date:  2007-09

9.  Effects of lapatinib on cell proliferation and apoptosis in NB4 cells.

Authors:  Lu Liu; Liang Zhong; Yi Zhao; Min Chen; Shifei Yao; Lianwen Li; Chunlan Xiao; Zhiling Shan; Liugen Gan; Ting Xu; Beizhong Liu
Journal:  Oncol Lett       Date:  2017-11-03       Impact factor: 2.967

10.  Lapatinib Inhibits Breast Cancer Cell Proliferation by Influencing PKM2 Expression.

Authors:  Mingxiu Guan; Yingna Tong; Minghua Guan; Xiaobin Liu; Meng Wang; Ruifang Niu; Fei Zhang; Dong Dong; Jie Shao; Yunli Zhou
Journal:  Technol Cancer Res Treat       Date:  2018-01-01
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.