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PMID: 20632056 Published · ppublish English Journal Article Review

Treatment strategy for HER2-positive breast cancer.

International journal of clinical oncology ·Vol. 15 ·No. 4 ·2010-08-00 ·Pages 335-40

Mukai H

Abstract

HER2-positive tumors account for approximately 18-20% of all breast cancers. These tumors tend to be more aggressive than HER2-negative tumors and are associated with a poorer prognosis. HER2 overexpression, as determined by either 3+ immunohistochemical staining for HER2 protein or HER2 gene amplification by fluorescence in situ hybridization, should be used to select patients for anti-HER2 therapy. Trastuzumab-containing regimens as first-line therapy should be recommended to women with HER2-positive metastatic breast cancer. The continuation of trastuzumab plus capecitabine provided a significant clinical benefit compared with capecitabine alone in women who experienced progression during trastuzumab treatment. An adjuvant trastuzumab-containing regimen should be also recommended to all intermediate- or high-risk women with HER2-positive early breast cancer. Cardiac function should be serially monitored during this treatment. Many anti-HER2 drugs against breast cancer are being developed. The basic mechanisms of their action and resistance emergence are being clarified step by step. Over the mid- or long term, clinical trials comparing these drugs will be conducted until drugs that are clinically effective and easy to use in the true sense survive. Biomarkers are being aggressively searched for concerning individual drugs under development. A position of the "proper drug for the proper patient" will be more firmly established.

MeSH Terms
Antibodies, Monoclonal/administration & dosage Antineoplastic Combined Chemotherapy Protocols/adverse effects,therapeutic use Biomarkers, Tumor/analysis,genetics Breast Neoplasms/chemistry,drug therapy,genetics,secondary Chemotherapy, Adjuvant Drug Resistance, Neoplasm Female Humans Precision Medicine Protein Kinase Inhibitors/administration & dosage Receptor, ErbB-2/analysis,antagonists & inhibitors,genetics Treatment Outcome
Chemicals
Antibodies, Monoclonal Biomarkers, Tumor Protein Kinase Inhibitors ERBB2 protein, human Receptor, ErbB-2
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Mukai Hirofumi
Division of Oncology/Hematology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba, Japan. [email protected]
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Article Info
Journal
International journal of clinical oncology
Abbr.
Int J Clin Oncol
ISSN
1437-7772
Published
2010-08-00
Epub
2010-00-15
Pages
335-40
Language
English
Region
Japan
NLM ID
9616295
Subset
IM
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