Targeted therapies for gynecologic malignancies

被引:4
作者
Hyde J. [1 ]
McMeekin D.S. [1 ]
机构
[1] University of Oklahoma-HSC, Oklahoma City, OK 73190
关键词
Epidermal Growth Factor Receptor; Bevacizumab; Imatinib; Trastuzumab; Endometrial Cancer;
D O I
10.1007/s11864-005-0020-3
中图分类号
学科分类号
摘要
Despite the enormous promise that targeted therapies hold for patients with gynecologic malignancies, it is far too early to recommend any targeted therapy outside of a clinical trial. There remains considerable work to be done before targeted therapies will have a significant role in this patient population. We have learned that different tumor types express different targets, but that the mere expression of a target does not necessarily correlate with benefit from the use of the targeted agent. No less important is the challenge of determining how these agents should be studied in clinical trials, and what constitutes an active agent. To document efficacy, targeted agents would hopefully produce response (ie, shrinkage of measurable tumor), but as cytostatic agents, the ability to delay tumor growth or slow the development of symptoms would be clinically important. Combining targeted therapies with cytotoxic agents, radiation, or other targeted therapies may be important areas for study, but it is essential to demonstrate the additive or synergistic effect of the targeted therapy to an already established active one. This review covers strategies used to develop targeted agents, reviews available targeted therapies, and suggests potential roles in the treatment of gynecologic cancers. Copyright © 2005 by Current Science Inc.
引用
收藏
页码:121 / 132
页数:11
相关论文
共 49 条
[1]  
Cancer Statistics 2004, (2004)
[2]  
Savage D., Antman K., Imatinib mesylate- A new oral targeted therapy, New Engl. J. Med., 356, pp. 683-693, (2002)
[3]  
Ball H.G., Blessing J.A., Lentz S.S., Mutch D.G., A phase II trial of paclitaxel in patients with advanced or recurrent adenocarcinoma of the endometrium: A Gynecologic Oncology Group Study, Gynecol. Oncol., 62, pp. 278-281, (1996)
[4]  
McMeekin D.S., Sill M., Benbrook D., Et al., A phase II study of thalidomide in patients with recurrent or persistent endometrial carcinoma: A Gynecologic Oncology Group (GOG) Study, Gynecol. Oncol., 92, (2004)
[5]  
Eisenhauer E., Phase I and II trials of novel anticancer agents: Endpoints, efficacy, and existentialism, Ann. Oncol., 9, pp. 1047-1052, (1998)
[6]  
Fox E., Curt G., Balis F., Clinical trial design for target-based therapy, Oncologist, 7, pp. 401-409, (2002)
[7]  
Druker B., Molecularly targeted therapy: Have the floodgates opened?, Oncologist, 9, pp. 357-360, (2004)
[8]  
Rosner G., Ratain M., Randomized discontinuation design: Applications to cytostatic antineoplastic agents, J. Clin. Oncol., 20, pp. 4478-4484, (2002)
[9]  
Macnard S., Pupa S., Campiglio M., Tagliabue E., Biologic and therapeutic role of HER2 in cancer, Oncogene, 22, pp. 6570-6578, (2003)
[10]  
Cobleigh M.A., Vogel C.L., Tripathy D., Et al., Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2 overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease, J. Clin. Oncol., 17, pp. 2639-2648, (1999)