» Articles » PMID: 15128006

Chemotherapy for Metastatic Breast Cancer

Overview
Date 2004 May 7
PMID 15128006
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose Of Review: This review is intended to summarize the most up-to-date information in the field of chemotherapy for advanced breast cancer.

Recent Findings: During the past year, the literature on chemotherapy for metastatic breast cancer has focused on three main areas of interest: the development of new cytotoxic agents with most studies addressing the taxane-pretreated population; the evaluation of new combination regimens, mainly incorporating a taxane; and the development of new trastuzumab-cytotoxic-agent combinations in the HER-2-positive population. In addition, interesting data regarding combination versus sequential single-agent chemotherapy and the optimal duration of chemotherapy have been published.

Summary: Interesting new drugs have faced phase II development. Randomized trials will define their role in the daily management of metastatic breast cancer. New combination regimens, generally incorporating a taxane, improve short-term efficacy in comparison with standard anthracycline-based combinations or single-agent chemotherapy, but at the cost of increased toxicity. Trastuzumab can be safely combined with several cytotoxic agents.

Citing Articles

Efficacy and safety of anticancer drug combinations: a meta-analysis of randomized trials with a focus on immunotherapeutics and gene-targeted compounds.

Jardim D, Gagliato D, Nikanjam M, Barkauskas D, Kurzrock R Oncoimmunology. 2020; 9(1):1710052.

PMID: 32002305 PMC: 6959453. DOI: 10.1080/2162402X.2019.1710052.


Different Expression of Extracellular Signal-Regulated Kinases (ERK) 1/2 and Phospho-Erk Proteins in MBA-MB-231 and MCF-7 Cells after Chemotherapy with Doxorubicin or Docetaxel.

Taherian A, Mazoochi T Iran J Basic Med Sci. 2013; 15(1):669-77.

PMID: 23493035 PMC: 3586869.


Salinomycin sensitizes cancer cells to the effects of doxorubicin and etoposide treatment by increasing DNA damage and reducing p21 protein.

Kim J, Chae M, Kim W, Kim Y, Kang H, Kim H Br J Pharmacol. 2010; 162(3):773-84.

PMID: 20973777 PMC: 3041264. DOI: 10.1111/j.1476-5381.2010.01089.x.


Luteinizing hormone-releasing hormone receptor-mediated delivery of mitoxantrone using LHRH analogs modified with PEGylated liposomes.

He Y, Zhang L, Song C Int J Nanomedicine. 2010; 5:697-705.

PMID: 20957221 PMC: 2948949. DOI: 10.2147/ijn.s12129.