Title of article :
Systemic therapy in metastatic or recurrent endometrial cancer
Author/Authors :
Pectasides، نويسنده , , D. and Pectasides، نويسنده , , E. and Economopoulos، نويسنده , , T.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
14
From page :
177
To page :
190
Abstract :
Summary trial cancer is one of the most common gynecologic malignancies. In patients with advanced or recurrent endometrial cancer survival is greatly diminished. Hormonal therapy and chemotherapy play a major role in the management of advanced or recurrent endometrial cancer. Endocrine therapy provides a 10–20% response rate (RR) and survival of less than 1 year. Combination chemotherapy offers a RR of 40–60%, but the survival is still less than 1 year. The combination of cisplatin plus doxorubicin is the most commonly used regimen, but carboplatin plus paclitaxel represents an efficacious, low toxicity regimen in advanced or recurrent endometrial cancer. The addition of paclitaxel to cisplatin plus doxorubicin appears to improve response rates, progression-free survival and overall survival, but to worsen toxicity profile. At this time the focus of future research should be on the use of novel targeted agents, since it is unlikely that further significant advances could be made with chemotherapy and endocrine therapy. mTOR inhibitors represent a promising therapeutic strategy for endometrial cancer. Anti-HER-2/neu targeted therapy might be a novel and attractive therapeutic option in patients with biologically aggressive variants (uterine serous papillary carcinoma, clear cell carcinoma) of endometrial cancer. Research in better understanding the signal transduction pathways in endometrial carcinogenesis will allow the development of specific and selective molecularly targeted inhibitors.
Keywords :
Targeted agents , chemotherapy , Endometrial carcinoma , Endocrine therapy
Journal title :
Cancer Treatment Reviews
Serial Year :
2007
Journal title :
Cancer Treatment Reviews
Record number :
1834919
Link To Document :
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