Literature DB >> 20503416

Novel targeted therapies in inflammatory breast cancer.

Massimo Cristofanilli1.   

Abstract

Inflammatory breast cancer (IBC) accounts for 1% to 5% of all breast cancer cases. Its aggressive biology is characterized by rapid disease progression and poor prognosis. To improve and standardize therapy for IBC, development of novel therapeutics to molecular targets of IBC is key. Trastuzumab treatment, an anti-HER2 humanized monoclonal antibody, has been demonstrated to improve the 3-year survival rate of patients with IBC (70.1% vs 53.3%; P = .0007). Another chemotherapeutic drug, lapatinib, a dual tyrosine inhibitor of epidermal growth factor (EGFR) and HER2 signaling, in combination with capecitabine demonstrated encouraging results, with a 51% decrease in disease progression. Further investigation is needed to confirm the efficacy of lapatinib. Copyright 2010 American Cancer Society.

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Year:  2010        PMID: 20503416     DOI: 10.1002/cncr.25172

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  4 in total

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Review 2.  Evolving therapies and FAK inhibitors for the treatment of cancer.

Authors:  Kelli Bullard Dunn; Melissa Heffler; Vita M Golubovskaya
Journal:  Anticancer Agents Med Chem       Date:  2010-12       Impact factor: 2.505

3.  Thrombin stimulation of inflammatory breast cancer cells leads to aggressiveness via the EGFR-PAR1-Pak1 pathway.

Authors:  Kazufumi Ohshiro; Tri M Bui-Nguyen; Reddy S Divijendra Natha; Arnold M Schwartz; Paul Levine; Rakesh Kumar
Journal:  Int J Biol Markers       Date:  2012-12-27       Impact factor: 2.659

4.  In Vitro Assessment of the Inflammatory Breast Cancer Cell Line SUM 149: Discovery of 2 Single Nucleotide Polymorphisms in the RNase L Gene.

Authors:  Brandon T Nokes; Heather E Cunliffe; Bonnie Lafleur; David W Mount; Robert B Livingston; Bernard W Futscher; Julie E Lang
Journal:  J Cancer       Date:  2013-01-10       Impact factor: 4.207

  4 in total

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