Optimal primary therapy of ovarian cancer

被引:82
作者
Bookman, M. A. [1 ,2 ]
机构
[1] Arizona Oncol, 603 N Wilmot Rd,151, Tucson, AZ 85711 USA
[2] US Oncol Res, Tucson, AZ USA
关键词
ovarian cancer; neoadjuvant; cytoreductive surgery; intraperitoneal; OPEN-LABEL; PACLITAXEL; CARBOPLATIN; MORTALITY; TRIAL;
D O I
10.1093/annonc/mdw088
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Epithelial ovarian cancer continues to have the highest case-fatality ratio of all gynecologic cancers, in spite of ongoing advances in risk-assessment, genomics, tumor biology, cytoreductive surgery, chemotherapy, and molecular-targeted interventions. Primary treatment options for advanced-stage disease not only should reflect current best standards, but also need to be tailored for individual patients, with consideration of local resources. Methods: Formulation of recommendations for optimal primary therapy based on a selective review of data from completed randomized trials, analysis of ongoing trials, and integration with current tumor biology, within the context of individualized clinical care. Recommendations were presented for discussion during an international meeting of experts in ovarian cancer treatment. Results: Key recommendations include full adjuvant therapy for early-stage high-grade serous cancer; tailored utilization of neoadjuvant chemotherapy based on patient comorbidities, extent of disease, and likelihood of achieving optimal surgical cytoreduction; preferred utilization of carboplatin with weekly paclitaxel as primary therapy; consideration of intraperitoneal cisplatin-based therapy in appropriate patients; avoidance of maintenance chemotherapy; lack of necessity for bevacizumab during primary chemotherapy and primary maintenance; acknowledgement of research opportunities and priorities. Conclusions: Integrated multidisciplinary care, including cytoreductive surgery and platinum-based chemotherapy, remain central to the optimal management of women with advanced-stage ovarian cancer. However, even with recent technical advances, the impact on disease-related mortality is limited, and more attention will be focused on the early integration of research, particularly with neoadjuvant chemotherapy and interval cytoreductive surgery.
引用
收藏
页码:58 / 62
页数:5
相关论文
共 15 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]   Better Therapeutic Trials in Ovarian Cancer [J].
Bookman, Michael A. ;
Gilks, C. Blake ;
Kohn, Elise C. ;
Kaplan, Karen O. ;
Huntsman, David ;
Aghajanian, Carol ;
Birrer, Michael J. ;
Ledermann, Jonathan A. ;
Oza, Amit M. ;
Swenerton, Kenneth D. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2014, 106 (04)
[3]   Rethinking ovarian cancer II: reducing mortality from high-grade serous ovarian cancer [J].
Bowtell, David D. ;
Boehm, Steffen ;
Ahmed, Ahmed A. ;
Aspuria, Paul-Joseph ;
Bast, Robert C., Jr. ;
Beral, Valerie ;
Berek, Jonathan S. ;
Birrer, Michael J. ;
Blagden, Sarah ;
Bookman, Michael A. ;
Brenton, James D. ;
Chiappinelli, Katherine B. ;
Martins, Filipe Correia ;
Coukos, George ;
Drapkin, Ronny ;
Edmondson, Richard ;
Fotopoulou, Christina ;
Gabra, Hani ;
Galon, Jerome ;
Gourley, Charlie ;
Heong, Valerie ;
Huntsman, David G. ;
Iwanicki, Marcin ;
Karlan, Beth Y. ;
Kaye, Allyson ;
Lengyel, Ernst ;
Levine, Douglas A. ;
Lu, Karen H. ;
McNeish, Iain A. ;
Menon, Usha ;
Narod, Steven A. ;
Nelson, Brad H. ;
Nephew, Kenneth P. ;
Pharoah, Paul ;
Powell, Daniel J., Jr. ;
Ramos, Pilar ;
Romero, Iris L. ;
Scott, Clare L. ;
Sood, Anil K. ;
Stronach, Euan A. ;
Balkwill, Frances R. .
NATURE REVIEWS CANCER, 2015, 15 (11) :668-679
[4]  
Chan J, 2013, INT J GYNECOL CANCER, V23
[5]   The potential benefit of 6 vs. 3 cycles of chemotherapy in subsets of women with early-stage high-risk epithelial ovarian cancer: An exploratory analysis of a Gynecologic Oncology Group study [J].
Chan, John K. ;
Tian, Chunqiao ;
Fleming, Gini F. ;
Monk, Bradley J. ;
Herzog, Thomas J. ;
Kapp, Daniel S. ;
Bell, Jeffrey .
GYNECOLOGIC ONCOLOGY, 2010, 116 (03) :301-306
[6]   Does Aggressive Surgery Improve Outcomes? Interaction Between Preoperative Disease Burden and Complex Surgery in Patients With Advanced-Stage Ovarian Cancer: An Analysis of GOG 182 [J].
Horowitz, Neil S. ;
Miller, Austin ;
Rungruang, Bunja ;
Richard, Scott D. ;
Rodriguez, Noah ;
Bookman, Michael A. ;
Hamilton, Chad A. ;
Krivak, Thomas C. ;
Maxwell, G. Larry .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (08) :937-+
[7]   Long-term results of dose-dense paclitaxel and carboplatin versus conventional paclitaxel and carboplatin for treatment of advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer (JGOG 3016): a randomised, controlled, open-label trial [J].
Katsumata, Noriyuki ;
Yasuda, Makoto ;
Isonishi, Seiji ;
Takahashi, Fumiaki ;
Michimae, Hirofumi ;
Kimura, Eizo ;
Aoki, Daisuke ;
Jobo, Toshiko ;
Kodama, Shoji ;
Terauchi, Fumitoshi ;
Sugiyama, Toru ;
Ochiai, Kazunori .
LANCET ONCOLOGY, 2013, 14 (10) :1020-1026
[8]   Society of Gynecologic Oncology statement on risk assessment for inherited gynecologic cancer predispositions [J].
Lancaster, Johnathan M. ;
Powell, C. Bethan ;
Chen, Lee-may ;
Richardson, Debra L. .
GYNECOLOGIC ONCOLOGY, 2015, 136 (01) :3-7
[9]   A randomized phase III trial of IV carboplatin and paclitaxel x 3 courses followed by observation versus weekly maintenance low-dose paclitaxel in patients with early-stage ovarian carcinoma: A Gynecologic Oncology Group Study [J].
Mannel, Robert S. ;
Brady, Mark F. ;
Kohn, Elise C. ;
Hanjani, Parviz ;
Hiura, Masamichi ;
Lee, Roger ;
DeGeest, Koen ;
Cohn, David E. ;
Monk, Bradley J. ;
Michael, Helen .
GYNECOLOGIC ONCOLOGY, 2011, 122 (01) :89-94
[10]   Phase II trial of weekly paclitaxel (80 mg/m2) in platinum and paclitaxel-resistant ovarian and primary peritoneal cancers:: A Gynecologic Oncology Group study [J].
Markman, Maurie ;
Blessing, John ;
Rubin, Stephen C. ;
Connor, Joseph ;
Hanjani, Parviz ;
Waggoner, Steven .
GYNECOLOGIC ONCOLOGY, 2006, 101 (03) :436-440