Intraperitoneal chemotherapy in the first-line treatment of women with stage III epithelial ovarian cancer - A systematic review with melaanalyses

被引:100
作者
Elit, Laurie
Oliver, Thomas K.
Covens, Allan
Kwon, Janice
Fung, Michael -Kee Fung
Hirte, Holger W.
Oza, Amit M.
机构
[1] McMaster Univ, Canc Care Ontario, Program Evidence Based Care, Dept Clin Epidemiol & Biostat, Hamilton, ON L8S 4L8, Canada
[2] Hamilton Reg Canc Ctr, Dept Obstet & Gynecol, Hamilton, ON L8V 1C3, Canada
[3] Toronto Sunnybrook Reg Canc Ctr, Dept Obstet & Gynecol, Toronto, ON, Canada
[4] London Hlth Sci Ctr, Dept Obstet & Gynecol, London, ON, Canada
[5] Ottawa Hosp, Reg Canc Ctr, Dept Obstet & Gynecol, Ottawa, ON, Canada
[6] Ottawa Hosp, Reg Canc Ctr, Dept Surg, Ottawa, ON, Canada
[7] Princess Margaret Hosp, Dept Obstet & Gynecol, Toronto, ON M4X 1K9, Canada
关键词
ovarian neoplasms; intraperitoneal; drug therapy; chemotherapy; systematic review;
D O I
10.1002/cncr.22466
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Because women with advanced ovarian cancer have poor outcomes, it is imperative to continue exploring for novel therapies. The opportunity for intraperitoneal treatment, especially in the subgroup of patients with minimal residual disease, in which the intraperitoneal approach may have a biologic rationale for benefit over and above the standard intravenous route, needs to be explored to the fullest extent. The MEDLINE, EMBASE, and Cochrane Library databases were searched up to January 2006 for randomized trials that compared first-line intraperitoneal-containing chemotherapy with first-line intravenous chemotherapy in the treatment of women with stage III epithelial ovarian cancer. Seven randomized, controlled trials were identified, including 3 large Phase III trials and 4 smaller randomized trials. The 3 large Phase III trials detected statistically significant overall survival benefits with intraperitoneal cisplatin-containing chemotherapy compared with intravenous chemotherapy alone. The improvements in survival were 8 months, 11 months, and 16 months, respectively. Pooled analysis from 6 of the 7 randomized trials confirmed the survival effect with intraperitoneal chemotherapy compared with intravenous chemotherapy alone (relative risk, 0.88; 95% confidence interval, 0.81-0.95). Severe adverse events and catheter-related complications with intraperitoneal chemotherapy were significantly more common and often were dose-limiting. The results from this review indicated that cisplatin-containing intraperitoneal chemotherapy should be offered to patients on the basis of significant improvements in overall survival. The appropriate clinical and institutional multidisciplinary facilities are needed for the safe delivery of this treatment in optimally debulked patients. Further research is needed concerning specific aspects of the treatment, such as optimal agent, dose, and scheduling.
引用
收藏
页码:692 / 702
页数:11
相关论文
共 24 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]   Intraperitoneal therapy for stage III ovarian cancer: A therapy whose time has come! [J].
Alberts, DS ;
Markman, M ;
Armstrong, D ;
Rothenberg, ML ;
Muggia, F ;
Howell, SB .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (19) :3944-3946
[3]   Intraperitoneal cisplatin and paclitaxel in ovarian cancer [J].
Armstrong, DK ;
Bundy, B ;
Wenzel, L ;
Huang, HQ ;
Baergen, R ;
Lele, S ;
Copeland, LJ ;
Walker, JL ;
Burger, RA .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (01) :34-43
[4]   Pharmacokinetic problems in peritoneal drug administration: Tissue penetration and surface exposure [J].
Dedrick, RL ;
Flessner, MF .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (07) :480-487
[5]   METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188
[6]   Preliminary toxicity analysis of intraperitoneal carboplatin in combination with intravenous paclitaxel chemotherapy for patients with carcinoma of the ovary, peritoneum, or fallopian tube [J].
Fujiwara, K ;
Suzuki, S ;
Ishikawa, H ;
Oda, T ;
Aotani, E ;
Kohno, I .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2005, 15 (03) :426-431
[7]   First-line intraperitoneal carboplatin-based chemotherapy for 165 patients with epithelial ovarian carcinoma: results of long-term follow-up (vol 90, pg 637, 2003) [J].
Fujiwara, K ;
Sakuragi, N ;
Suzuki, S ;
Yoshida, N ;
Maehata, K ;
Nishiya, M ;
Koshida, T ;
Sawai, H ;
Aotani, E ;
Kohno, I .
GYNECOLOGIC ONCOLOGY, 2003, 91 (03) :662-662
[8]   Intraperitoneal versus intravenous cisplatin in combination with intravenous cyclophosphamide and epidoxorubicin in optimally cytoreduced advanced epithelial ovarian cancer: A randomized trial of the Gruppo Oncologico Noud-Ovest [J].
Gadducci, A ;
Carnino, F ;
Chiara, S ;
Brunetti, I ;
Tanganelli, L ;
Romanini, A ;
Bruzzone, M ;
Conte, PF .
GYNECOLOGIC ONCOLOGY, 2000, 76 (02) :157-162
[9]   Epithelial ovarian cancer: A review of current management [J].
Guppy, AE ;
Nathan, PD ;
Rustin, GJS .
CLINICAL ONCOLOGY, 2005, 17 (06) :399-411
[10]   A COMPARISON OF INTRAVENOUS VERSUS INTRAPERITONEAL CHEMOTHERAPY FOR THE INITIAL TREATMENT OF OVARIAN-CANCER [J].
KIRMANI, S ;
BRALY, PS ;
MCCLAY, EF ;
SALTZSTEIN, SL ;
PLAXE, SC ;
KIM, S ;
CATES, C ;
HOWELL, SB .
GYNECOLOGIC ONCOLOGY, 1994, 54 (03) :338-344