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Review
. 2010;15(10):1026-33.
doi: 10.1634/theoncologist.2010-0087. Epub 2010 Oct 7.

Endometrial carcinoma: a review of chemotherapy, drug resistance, and the search for new agents

Affiliations
Review

Endometrial carcinoma: a review of chemotherapy, drug resistance, and the search for new agents

Katherine M Moxley et al. Oncologist. 2010.

Abstract

Adenocarcinoma of the endometrium represents the most common gynecologic malignancy in developed countries. Although early-stage cancers are effectively treated surgically, commonly without adjuvant therapy, the treatment of high-risk and advanced disease is more complex. Chemotherapy has evolved into an important modality in high-risk early-stage and advanced-stage disease, and in recurrent endometrial cancer. Taxane-based therapy consistently demonstrates the highest response rates in the first-line and salvage settings of endometrial cancer. Unfortunately, response to chemotherapy is modest and strategies are needed to predict chemotherapy-responsive and chemotherapy-resistant populations. Chemotherapy resistance mediated by overexpression of drug efflux pump proteins and mutations in β-tubulin isoforms in both primary and recurrent disease represent unique treatment challenges and highlight the need for new agents that are less susceptible to these known resistance pathways. Epothilone B analogs are novel cytotoxic agents with activity in solid tumors, including advanced/recurrent endometrial carcinoma, and may have unique properties that can overcome resistance in some settings. These agents alone and in combination represent a new therapeutic opportunity in endometrial carcinoma.

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Conflict of interest statement

Disclosures: Katherine M. Moxley: None; D. Scott McMeekin: Consultant/advisory role: Bristol-Myers Squibb.

The article discusses epothilones in the context of endometrial cancer, for which they are not approved.

The content of this article has been reviewed by independent peer reviewers to ensure that it is balanced, objective, and free from commercial bias. No financial relationships relevant to the content of this article have been disclosed by the independent peer reviewers.

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