Endocrine therapy in ovarian cancer: where do we stand?

被引:15
作者
Paleari, Laura [1 ,2 ]
DeCensi, Andrea [1 ,3 ]
机构
[1] EO Osped Galliera, Div Med Oncol, Via Volta 6, I-16128 Genoa, Italy
[2] Publ Hlth Agcy, ALiSa, Genoa, Italy
[3] Queen Mary Univ London, Wolfson Inst Prevent Med, Barts & London Sch Med & Dent, London, England
关键词
clinical benefit; endocrine therapy; epithelial ovarian cancer; ESTROGEN-RECEPTOR EXPRESSION; PHASE-II TRIAL; EPITHELIAL OVARIAN; PLATINUM-RESISTANT; TAMOXIFEN THERAPY; ANTIESTROGEN THERAPY; HORMONAL-THERAPY; LETROZOLE; CARCINOMA; WOMEN;
D O I
10.1097/GCO.0000000000000423
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Purpose of review Hormonal factors play a pivotal role in epithelial ovarian tumorigenesis and steroid receptor expression has been associated with epithelial ovarian cancer (EOC) response and survival in recent studies. However, the degree of activity of endocrine therapy overall and by specific agents remains unclear. The purpose of this work is to summarize the evidence provided by the recent literature on the effectiveness of endocrine treatment for advanced EOC. Recent findings The results of 53 trials of different endocrine therapies in EOC indicate a clinical benefit of 41% [95% confidence interval (CI), 0.34-0.48], with a trend for a higher benefit in those with estrogen receptor (ER) thorn and/or progesteron receptor (PgR) + tumors. Moreover, the odd ratio for death showed a reduced mortality with endocrine regimens (0.69, 95% CI, 0.50-0.97), with a propensity for a better outcome in first-line and low-grade tumors. Summary We suggest that ER and PgR have a predictive role and their inhibition by endocrine therapy may be a treatment option for EOC. Randomized clinical trials in the first-line treatment of advanced hormone receptor positive EOC are warranted given the potential cost effectiveness of this approach.
引用
收藏
页码:17 / 22
页数:6
相关论文
共 57 条
[1]   HORMONAL PALLIATION OF CHEMORESISTANT OVARIAN-CANCER - 3 CONSECUTIVE PHASE-II TRIALS OF THE MID-ATLANTIC ONCOLOGY PROGRAM [J].
AHLGREN, JD ;
ELLISON, NM ;
GOTTLIEB, RJ ;
LALUNA, F ;
LOKICH, JJ ;
SINCLAIR, PR ;
UENO, W ;
WAMPLER, GL ;
YEUNG, KY ;
ALT, D ;
FRYER, JG .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (10) :1957-1968
[2]  
[Anonymous], 2010, COCHRANE DATABASE SY
[3]  
[Anonymous], INT J GYNECOLOGIC S1
[4]  
[Anonymous], AM SOC CLIN ONCOL
[5]  
[Anonymous], P 2 EUR C CLIN ONC
[6]  
[Anonymous], P 11 CLIN ONC SOC AU
[7]  
[Anonymous], P AM SOC CLIN ONCOL
[8]  
[Anonymous], P 11 CLIN ONC SOC AU
[9]  
[Anonymous], CHEMIOTERAPIA
[10]  
[Anonymous], 2005, J CLIN ONCOL S