Intraperitoneal treatment and dose-intense therapy in ovarian cancer

被引:20
作者
Ozols, RF
Gore, M
Tropé, C
Grenman, S
机构
[1] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[2] Royal Marsden Hosp, Dept Med, London SW3 6JJ, England
[3] Norwegian Radium Hosp, N-0310 Oslo, Norway
[4] Turku Univ, Cent Hosp, Dept Obstet & Gynecol, Turku, Finland
关键词
ovarian cancer; dose intensity; peripheral stem cell transplantation; autologous bone marrow transplantation; intraperitoneal therapy;
D O I
10.1023/A:1008363519331
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There has been a longstanding controversy regarding the role of high-dose chemotherapy in patients with advanced ovarian cancer. Based on retrospective studies, it has been suggested that there will be improved results when doses of platinum compounds in particular are increased. High-dose therapy can be administered using an intraperitoneal route of drug delivery or with haematologic support in the form of autologous bone marrow transplantation (ABMT) or peripheral blood stem cell transfusions (PBSCT). Methods: Experienced clinical investigators reviewed published data available on high-dose chemotherapy and intraperitoneal drug delivery. In addition, ongoing clinical trials of ABMT or PBSCT were also reviewed. Results: Prospective randomised trials have failed to demonstrate that doubling the dose of platinum compounds increases survival in patients with advanced ovarian cancer. Intraperitoneal chemotherapy with cisplatin or paclitaxel remains an area of investigation and prospective randomised trials in previously untreated patients as well as part of consolidation therapy in patients achieving a complete remission are in progress. Phase II trials of high-dose chemotherapy with ABMT or PBSCT in previously treated patients with advanced ovarian cancer have produced higher response rates than achieved with conventional doses although there has been no proven impact upon survival. Prospective randomised trials in previously untreated patients are in progress. Until the completion of these trials, high-dose chemotherapy with ABMT or PBSCT and intraperitoneal chemotherapy should be considered investigational.
引用
收藏
页码:59 / 64
页数:6
相关论文
共 33 条
[1]   Phase II study of "dose-dense" high-dose chemotherapy treatment with peripheral-blood progenitor-cell support as primary treatment for patients with advanced ovarian cancer [J].
Aghajanian, C ;
Fennelly, D ;
Shapiro, F ;
Waltzman, R ;
Almadrones, L ;
O'Flaherty, C ;
O'Conner, K ;
Venkatraman, E ;
Barakat, R ;
Curtin, J ;
Brown, C ;
Reich, L ;
Wuest, D ;
Norton, L ;
Hoskins, W ;
Spriggs, DR .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (05) :1852-1860
[2]   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
[3]  
BELLA M, 1994, ANN ONCOL S8, V5, P23
[4]   Very high-dose chemotherapy with autologous peripheral stem cell support in advanced ovarian cancer [J].
BenedettiPanici, P ;
Greggi, S ;
Scambia, G ;
Salerno, MG ;
Baiocchi, G ;
Laurelli, G ;
Menichella, G ;
Pierelli, L ;
Foddai, ML ;
Serafini, R ;
Bizzi, B ;
Mancuso, S .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (12) :1987-1992
[5]  
COLOMBO N, 1993, P AN M AM SOC CLIN, V12, P255
[6]   High-dose versus low-dose cisplatin in combination with cyclophosphamide and epidoxorubicin in suboptimal ovarian cancer: A randomized study of the gruppo oncologico nord-ovest [J].
Conte, PF ;
Bruzzone, M ;
Carnino, F ;
Gadducci, A ;
Algeri, R ;
Bellini, A ;
Boccardo, F ;
Brunetti, I ;
Catsafados, E ;
Chiara, S ;
Foglia, G ;
Gallo, I ;
Iskra, L ;
Mammoliti, S ;
Parodi, G ;
Ragni, N ;
Rosso, R ;
Rugiati, S ;
Rubagotti, A .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (02) :351-356
[7]  
DEVRIES EGE, 1993, ANN ONCOL S, V4, pS57
[8]  
DITTRICH C, 1996, P AN M AM SOC CLIN, V15, P749
[9]  
ENRLICK CE, 1983, CLIN OSBTN GYNAECOL, V10, P325
[10]  
FENELLY D, 1995, J CLIN ONCOL, V13, P1160