Treatment of metastatic cervical cancer: Future directions involving targeted agents

被引:86
作者
Diaz-Padilla, Ivan [1 ,2 ]
Monk, Bradley J. [3 ]
Mackay, Helen J. [1 ]
Oaknin, Ana [4 ]
机构
[1] Univ Toronto, Princess Margaret Hosp, Div Med Oncol & Hematol, Toronto, ON M5G 2M9, Canada
[2] Hosp Univ Madrid, Div Med Oncol, Ctr Integral Oncol Clara Campal, Madrid 28050, Spain
[3] Creighton Univ, Sch Med, St Josephs Hosp & Med Ctr, Div Gynecol Oncol,Dept Obstet & Gynecol, Phoenix, AZ 85013 USA
[4] Hosp Univ Vall dHebron, Div Med Oncol, Barcelona 08035, Spain
关键词
Metastatic cervical cancer; Targeted therapy; Human papilloma virus; Angiogenesis; Clinical trial; ENDOTHELIAL GROWTH-FACTOR; SQUAMOUS-CELL-CARCINOMA; GYNECOLOGIC-ONCOLOGY-GROUP; PHASE-II TRIAL; HUMAN-PAPILLOMAVIRUS TYPE-16; HUMAN MONOCLONAL-ANTIBODY; CHK1 CHECKPOINT KINASES; QUALITY-OF-LIFE; FACTOR RECEPTOR; UTERINE CERVIX;
D O I
10.1016/j.critrevonc.2012.07.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cervical cancer is the third most common cause of female cancer mortality, and it remains a major health problem in populations with limited economic resources. Metastatic disease or recurrent lesions not amenable to radical local excision or regional radiation have a poor prognosis, and are treated with palliative platinum-based chemotherapy. There are few effective therapeutic options for patients who progressed after first-line chemotherapy. Future advances in the treatment of metastatic or recurrent disease may rely on more effective and better-tolerated therapies, and molecularly driven targeted agents could represent an attractive option. Inhibition of tumor angiogenesis and epidermal growth factor receptor directed therapies have focused the most recent clinical research efforts. A thorough molecular characterization of cervical cancer remains crucial for a rationale implementation of targeted agents and companion biomarkers. Alternative clinical trial designs may also be necessary to optimize the clinical development of new drugs for metastatic cervical cancer. (c) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:303 / 314
页数:12
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