Future options for first-line therapy of advanced ovarian cancer

被引:45
作者
Du Bois, A
Pfisterer, J
机构
[1] Dr Horst Schmidt Klin HSK, Dept Gynecol & Gynecol Oncol, D-65199 Wiesbaden, Germany
[2] Univ Klinikum Schleswig Holstein, Klin Gynakol & Geburtshilfe, Wiesbaden, Germany
关键词
advanced ovarian cancer; chemotherapy; future options;
D O I
10.1111/j.1525-1438.2005.15356.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The current standard of treatment for patients with advanced ovarian cancer has been established in light of the results from various clinical trials. After debulking surgery, a combination of carboplatin and paclitaxel is considered to be the best treatment option in terms of survival and quality of life. However, since most patients on this chemotherapy modality will experience relapse, several studies have explored, and continue to do so, various modifications and alternatives to standard therapy in order to attain improved efficacy. Various modifications of dose, schedule, or route of standard regimens have shown no benefit, apart from intraperitoneal therapy, which has produced mixed results and would benefit from a definitive trial. Studies of maintenance/consolidation therapy have been mainly negative, although a small number of trials have produced enough positive data to prompt two new studies powered to detect survival benefits. Various phase II trials have investigated "targeted therapies," but until now no positive results have been recorded. Translational studies are needed to identify patients who will benefit from such specific treatment strategies. The current most evaluated modification of standard therapy is the addition of a third non-cross-resistant drug to carboplatin and paclitaxel. Data for the addition of anthracyclines have either been negative (epirubicin) or not yet analyzed (pegylated liposomal doxorubicin), while evaluable data are shortly expected for the addition of topotecan. Data on the addition of gemcitabine are eagerly awaited from two phase III trials.
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收藏
页码:42 / 50
页数:9
相关论文
共 48 条
[1]   Intraperitoneal cisplatin plus intravenous cyclophosphamide versus intravenous cisplatin plus intravenous cyclophosphamide for stage III ovarian cancer [J].
Alberts, DS ;
Liu, PY ;
Hannigan, EV ;
OToole, R ;
Williams, SD ;
Young, JA ;
Franklin, EW ;
ClarkePearson, DL ;
Malviya, VK ;
DuBeshter, B ;
Adelson, MD ;
Hoskins, WJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (26) :1950-1955
[2]  
Armstrong DK, 2002, P AN M AM SOC CLIN, V21, p201a
[3]   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
[4]   Optimal therapy of advanced ovarian cancer: carboplatin and paclitaxel vs. cisplatin and paclitaxel (GOG158) and an update on GOG0 182-ICON5 [J].
Bookman, MA ;
Greer, BE ;
Ozols, RF .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2003, 13 (06) :735-740
[5]   Evaluation of monoclonal humanized anti-HER2 antibody, trastuzumab, in patients with recurrent or refractory ovarian or primary peritoneal carcinoma with overexpression of HER2: A phase II trial of the Gynecologic Oncology Group [J].
Bookman, MA ;
Darcy, KM ;
Clarke-Pearson, D ;
Boothby, RA ;
Horowitz, IR .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (02) :283-290
[6]   CHEMOTHERAPY VERSUS RADIOTHERAPY IN THE MANAGEMENT OF OVARIAN-CANCER PATIENTS WITH PATHOLOGICAL COMPLETE RESPONSE OR MINIMAL RESIDUAL DISEASE AT 2ND LOOK [J].
BRUZZONE, M ;
REPETTO, L ;
CHIARA, S ;
CAMPORA, E ;
CONTE, PF ;
ORSATTI, M ;
VITALE, V ;
RUBAGOTTI, A ;
ROSSO, R .
GYNECOLOGIC ONCOLOGY, 1990, 38 (03) :392-395
[7]  
CURE H, 2004, J CLIN ONCOL S14, V22
[8]   Topotecan compared with no therapy after response to surgery and carboplatin/paclitaxel in patients with ovarian cancer: Multicenter Italian trials in ovarian cancer (MITO-1) randomized study [J].
De Placido, S ;
Scambia, G ;
Di Vagno, G ;
Naglieri, E ;
Lombardi, AV ;
Biamonte, R ;
Marinaccio, M ;
Carteni, G ;
Manzione, L ;
Febbraro, A ;
de Matteis, A ;
Gasparini, G ;
Valerio, MR ;
Danese, S ;
Perrone, F ;
Lauria, R ;
De Laurentiis, M ;
Greggi, S ;
Gallo, C ;
Pignata, S .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (13) :2635-2642
[9]   A phase II study of paclitaxel, carboplatin, and gemcitabine in previously untreated patients with epithelial ovarian cancer FIGO stage IC-IV (AGO-OVAR protocol OVAR-8) [J].
du Bois, A ;
Belau, A ;
Wagner, U ;
Pfisterer, J ;
Schmalfeldt, B ;
Richter, B ;
Staehle, A ;
Jackisch, C ;
Lueck, HJ ;
Schroeder, W ;
Burges, A ;
Olbricht, S ;
Elser, G .
GYNECOLOGIC ONCOLOGY, 2005, 96 (02) :444-451
[10]   A randomized clinical trial of cisplatin/paclitaxel versus carboplatin/paclitaxel as first-line treatment of ovarian cancer [J].
du Bois, A ;
Lück, HJ ;
Meier, W ;
Adams, HP ;
Möbus, V ;
Costa, S ;
Bauknecht, T ;
Richter, B ;
Warm, M ;
Schröder, W ;
Olbricht, S ;
Nitz, U ;
Jackisch, C ;
Emons, G ;
Wagner, U ;
Kuhn, W ;
Pfisterer, J .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (17) :1320-1330