Novel agents in ovarian cancer

被引:10
作者
Matei, Daniela
机构
[1] Indiana Univ, Sch Med, Div Hematol Oncol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Obstet & Gynecol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Indiana Univ Canc Ctr, Indianapolis, IN 46202 USA
[4] Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
关键词
angiogenesis; biological agents; clinical trials; ovarian cancer; Phase; 1; 11; targeted treatment;
D O I
10.1517/13543784.16.8.1227
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The standard treatment for epithelial ovarian cancer remains surgical debulking and chemotherapy with carboplatin and paclitaxel. However, the majority of patients relapse, and few, if any, achieve a cure. Future advancement in treatment should aim at targeting the biology of the disease, specifically mechanisms critical to tumor initiation and progression. Several Phase I and 11 clinical trials have identified novel opportunities for therapy. The most promising venues appear to be the antiangiogenic agents and the inhibitors of intracellular signaling. Novel modalities of delivering cytotoxics to tumor cells by exploiting ovarian cancer-specific biomarkers are also being tested, and appear promising. Immunomodulatory agents are being developed for consolidation therapy. Although devoid of the common side effects associated with chemotherapy, the use of targeted agents is associated with specific toxicities, related to the biological processes they block. The main challenge for future successful clinical development will be defining molecular markers predictive of response and judicious patient selection based on the biological features of the tumor. Individualized treatment driven by molecular characteristics will open the door to a new age in anticancer medicine.
引用
收藏
页码:1227 / 1239
页数:13
相关论文
共 149 条
[1]  
Adjei AA, 2003, CLIN CANCER RES, V9, P2520
[2]  
AGHAJANIAN PS, 2005, J CLIN ONCOL S, V23, P5047
[3]   Phase I clinical study of pertuzumab, a novel HER dimerization inhibitor, in patients with advanced cancer [J].
Agus, DB ;
Gordon, MS ;
Taylor, C ;
Natale, RB ;
Karlan, B ;
Mendelson, DS ;
Press, MF ;
Allison, DE ;
Sliwkowski, MX ;
Lieberman, G ;
Kelsey, SM ;
Fyfe, G .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2534-2543
[4]   Expression of platelet-derived growth factor and activated receptor in clinical specimens of epithelial ovarian cancer and ovarian carcinoma cell lines [J].
Apte, SM ;
Bucana, CD ;
Killion, JJ ;
Gershenson, DM ;
Fidler, IJ .
GYNECOLOGIC ONCOLOGY, 2004, 93 (01) :78-86
[5]  
AUERSPERG N, 1994, LAB INVEST, V71, P510
[6]   Current research and treatment for epithelial ovarian cancer - A Position Paper from the Helene Harris Memorial Trust [J].
Balkwill, F ;
Bast, RC ;
Berek, J ;
Chenevix-Trench, G ;
Gore, M ;
Hamilton, T ;
Jacobs, I ;
Mills, G ;
Souhami, R ;
Urban, N ;
Ursulic, S ;
Smyth, J .
EUROPEAN JOURNAL OF CANCER, 2003, 39 (13) :1818-1827
[7]   MOLECULAR ALTERATIONS OF THE AKT2 ONCOGENE IN OVARIAN AND BREAST CARCINOMAS [J].
BELLACOSA, A ;
DEFEO, D ;
GODWIN, AK ;
BELL, DW ;
CHENG, JQ ;
ALTOMARE, DA ;
WAN, MH ;
DUBEAU, L ;
SCAMBIA, G ;
MASCIULLO, V ;
FERRANDINA, G ;
PANICI, PB ;
MANCUSO, S ;
NERI, G ;
TESTA, JR .
INTERNATIONAL JOURNAL OF CANCER, 1995, 64 (04) :280-285
[8]  
BERCHUCK A, 1990, CANCER RES, V50, P4087
[9]   Advanced epithelial ovarian cancer:: 1998 consensus statements [J].
Berek, JS ;
Bertelsen, K ;
du Bois, A ;
Brady, MF ;
Carmichael, J ;
Eisenhauer, EA ;
Gore, M ;
Grenman, S ;
Hamilton, TC ;
Hansen, SW ;
Harper, PG ;
Horvath, G ;
Kaye, SB ;
Lück, HJ ;
Lund, B ;
McGuire, WP ;
Neijt, JP ;
Ozols, RF ;
Parmar, MKB ;
Piccart-Gebhart, MJ ;
van Rijswijk, R ;
Rosenberg, P ;
Rustin, GJS ;
Sessa, C ;
Thigpen, JT ;
Tropé, C ;
Tuxen, MK ;
Vergote, I ;
Vermorken, JB ;
Willemse, PHB .
ANNALS OF ONCOLOGY, 1999, 10 :87-92
[10]   Randomized, placebo-controlled study of oregovomab for consolidation of clinical remission in patients with advanced ovarian cancer [J].
Berek, JS ;
Taylor, PT ;
Gordon, A ;
Cunningham, MJ ;
Finkler, N ;
Orr, J ;
Rivkin, S ;
Schultes, BC ;
Whiteside, TL ;
Nicodemus, CF .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (17) :3507-3516