Survival impact of complete cytoreduction to no gross residual disease for advanced-stage ovarian cancer: A meta-analysis

被引:397
作者
Chang, Suk-Joon [1 ]
Hodeib, Melissa [2 ]
Chang, Jenny [3 ]
Bristow, Robert E. [2 ]
机构
[1] Ajou Univ, Sch Med, Dept Obstet & Gynecol, Suwon 441749, South Korea
[2] Univ Calif Irvine, Sch Med, Dept Obstet & Gynecol, Div Gynecol Oncol, Orange, CA 92868 USA
[3] Univ Calif Irvine, Dept Epidemiol, Irvine, CA USA
关键词
Advanced ovarian cancer; Complete cytoreduction; Residual disease; PHASE-III TRIAL; INTRAVENOUS CISPLATIN PLUS; GYNECOLOGIC-ONCOLOGY-GROUP; 1ST-LINE TREATMENT; PROGNOSTIC-FACTORS; INTERGROUP TRIAL; INTRAPERITONEAL CISPLATIN; SURGICAL CYTOREDUCTION; RANDOMIZED-TRIAL; DES CANCERS;
D O I
10.1016/j.ygyno.2013.05.040
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objective. To quantify the impact of complete cytoreduction to no gross residual disease on overall survival among patients with advanced-stage ovarian cancer treated during the platinum-taxane era. Methods. PubMed and Cochrane Library databases were searched for all articles on primary cytoreductive surgery for advanced-stage ovarian cancer published from 1/1996 to 7/2011. A total of 18 relevant studies (13,257 patients) were identified for analysis. Simple and multiple linear regression analyses, with weighted correlation calculations, were used to assess the effect on median survival time of clinical and treatment-related factors. Results. The mean weighted median overall survival time for all cohorts was 44.4 months (range, 27.6-66.9 months). Simple linear regression analysis revealed that residual disease, stage IV disease, and use of intraperitoneal chemotherapy were significantly associated with median survival time. After controlling for other factors on multiple linear regression analysis, each 10% increase in the proportion of patients undergoing complete cytoreduction to no gross residual disease was associated with a significant and independent 2.3-month increase (95%Cl = 0.6-4.0, p = 0.011) in cohort median survival compared to a 1.8-month increase (95%Cl = 0.6-3.0, p = 0.004) in cohort median survival for optimal cytoreduction (residual disease 1 cm). Each 10% increase in the proportion of patients receiving intraperitoneal chemotherapy was associated with a significant and independent 3.9-month increase (95%C1 = 1.1-6.8, p = 0.008) in median cohort survival time. Conclusions. For advanced-stage ovarian cancer treated during the platinum-taxane era, the proportions of patients left with no gross residual disease and receiving intraperitoneal chemotherapy are independently significant factors associated with the most favorable cohort survival time. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:493 / 498
页数:6
相关论文
共 40 条
[1]
Aggressive surgical effort and improved survival in advanced-stage ovarian cancer [J].
Aletti, GD ;
Dowdy, SC ;
Gostout, BS ;
Jones, MB ;
Stanhope, CR ;
Wilson, TO ;
Podratz, KC ;
Cliby, WA .
OBSTETRICS AND GYNECOLOGY, 2006, 107 (01) :77-85
[2]
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
[3]
METAANALYSIS COMPARING CISPLATIN TOTAL-DOSE INTENSITY AND SURVIVAL [J].
BENDAVID, Y ;
ROSEN, B ;
FRANSSEN, E ;
EINARSON, T ;
SZYFER, I .
GYNECOLOGIC ONCOLOGY, 1995, 59 (01) :93-101
[4]
Evaluation of New Platinum-Based Treatment Regimens in Advanced-Stage Ovarian Cancer: A Phase III Trial of the Gynecologic Cancer InterGroup [J].
Bookman, Michael A. ;
Brady, Mark F. ;
McGuire, William P. ;
Harper, Peter G. ;
Alberts, David S. ;
Friedlander, Michael ;
Colombo, Nicoletta ;
Fowler, Jeffrey M. ;
Argenta, Peter A. ;
De Geest, Koen ;
Mutch, David G. ;
Burger, Robert A. ;
Swart, Ann Marie ;
Trimble, Edward L. ;
Accario-Winslow, Chrisann ;
Roth, Lawrence M. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (09) :1419-1425
[5]
Survival effect of maximal cytoreductive surgery for advanced ovarian carcinoma during the platinum era: A meta-analysis [J].
Bristow, RE ;
Tomacruz, RS ;
Armstrong, DK ;
Trimble, EL ;
Montz, FJ .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (05) :1248-1259
[6]
Evolution of surgical treatment paradigms for advanced-stage ovarian cancer: Redefining 'optimal' residual disease [J].
Chang, Suk-Joon ;
Bristow, Robert E. .
GYNECOLOGIC ONCOLOGY, 2012, 125 (02) :483-492
[7]
What is the optimal goal of primary cytoreductive surgery for bulky stage IIIC epithelial ovarian carcinoma (EOC)? [J].
Chi, D. S. ;
Eisenhauer, E. L. ;
Lang, J. ;
Huh, J. ;
Haddad, L. ;
Abu-Rustum, N. R. ;
Sonoda, Y. ;
Levine, D. A. ;
Hensley, M. ;
Barakat, R. R. .
GYNECOLOGIC ONCOLOGY, 2006, 103 (02) :559-564
[8]
Does aggressive surgery only benefit patients with less advanced ovarian cancer? Results from an international comparison within the SCOTROC-1 Trial [J].
Crawford, SC ;
Vasey, PA ;
Paul, J ;
Hay, A ;
Davis, JA ;
Kaye, SB .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (34) :8802-8811
[9]
Addition of epirubicin as a third drug to carboplatin-paclitaxel in first-line treatment of advanced ovarian cancer: A prospectively randomized gynecologic cancer intergroup trial by the Arbeitsgemeinschaft Gynaekologische Onkologie Ovarian Cancer Study Group and the Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens [J].
du Bois, A ;
Weber, B ;
Rochon, J ;
Meier, W ;
Goupil, A ;
Bricht, S ;
Barats, JC ;
Kuhn, W ;
Orfeuvre, H ;
Wagner, U ;
Richter, B ;
Lueck, HJ ;
Pfisterer, J ;
Costa, S ;
Schroeder, W ;
Kimmig, R ;
Pujade-Lauraine, E .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (07) :1127-1135
[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