Targeting human epidermal growth factor receptor 2 (HER2) in gynecologic malignancies

被引:38
作者
Erickson, Britt K. [1 ]
Zeybek, Burak [2 ]
Santin, Alessandro D. [2 ]
Fader, Amanda N. [3 ]
机构
[1] Univ Minnesota, Div Gynecol Oncol, MMC 395,420 Delaware St SE, Minneapolis, MN 55455 USA
[2] Yale Univ, Div Gynecol Oncol, New Haven, CT USA
[3] Johns Hopkins Univ, Div Gynecol Oncol, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
biomarker; human epidermal growth factor receptor 2; ovarian cancer; uterine serous carcinoma; UTERINE SEROUS CARCINOMA; PHASE-II TRIAL; IN-VITRO; HER2-TARGETED THERAPIES; ACQUIRED-RESISTANCE; ENDOMETRIAL CANCER; IMPACTS SURVIVAL; DRUG CONJUGATE; LARGE COHORT; AMPLIFICATION;
D O I
10.1097/GCO.0000000000000599
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Purpose of review The purpose of this review is to describe the role of the human epidermal growth factor receptor 2 (HER2) as a biomarker and potential target in gynecologic malignancies and to describe contemporary updates in the use of anti-HER2 treatments for these cancers. Recent findings Approximately 25-30% of all patients with uterine serous carcinoma overexpress tumoral HER2. The anti-HER2 antibody trastuzumab represents an effective, targeted therapy with significant efficacy in the treatment of HER2-positive breast and gastric cancer. Recently, trastuzumab efficacy has also been demonstrated in a randomized controlled trial of women with advanced or recurrent uterine serous carcinoma. Additionally, trastuzumab may be effective in women with HER2-positive uterine carcinosarcoma. The role of anti-HER2 therapy is unclear in women with other gynecologic malignancies but is being evaluated. HER2 amplification/overexpression is an effective therapeutic target in select gynecologic malignancies, and especially in the rare endometrial cancer subtype, uterine serous carcinoma. As anti-HER2-targeted therapies become increasingly available, more treatment options may become available for women with HER2-positive disease.
引用
收藏
页码:57 / 64
页数:8
相关论文
共 60 条
[21]  
[Anonymous], 2012, NEW ENGL J MED, DOI DOI 10.1056/NEJMOA1209124
[22]  
[Anonymous], 2012, CRIT REV ONCOGENES 1
[23]  
[Anonymous], 2007, NATURE, DOI DOI 10.1038/NATURE05474
[24]  
[Anonymous], 2017, J MOL DIAGN, DOI DOI 10.1016/J.JMOLDX.2016.09.010
[25]  
[Anonymous], 2015, BRIT J CANCER, DOI DOI 10.1038/BJC.2015.388
[26]  
[Anonymous], 2007, ONCOGENE, DOI DOI 10.1038/SJ.ONC.1210477
[27]  
[Anonymous], 2017, INT J GYNECOL PATHOL, DOI DOI 10.1097/PGP.0000000000000338
[28]  
[Anonymous], 2008, GYNECOL ONCOL, DOI DOI 10.1016/J.YGYNO.2007.09.007
[29]  
[Anonymous], 2009, CANCER AM CANCER SOC, DOI DOI 10.1002/CNCR.24247
[30]  
[Anonymous], 2016, MOL CANCER THER, DOI DOI 10.1158/1535-7163.MCT-16-0163