Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Ovarian cancer Stage III C. Consequences of treatment level on overall and progression-free survival
1Department of Operative Treatment, Gynaecology, The Norwegian Radium Hospital, Norway
2Medical faculty of the University of Oslo, Norway
3Office for Clinical Research, The Norwegian Radium Hospital and the Norwegian Cancer Association, Montebello, Norway
*Corresponding Author(s): H. OKSEFJELL E-mail:
Background: Maximum cytoreduction at primary surgery has been found to be one of the strongest prognostic factors for survival of ovarian cancer. The aim of the study was to investigate the influence of hospital level (primary vs secondary care centre), number and timing of surgery and chemotherapy on how radical the surgery was at primary treatment of epithelial ovarian cancer Stage IIIC.
Material and methods: A retrospective study based on record information from all patients with epithelial ovarian cancer Stage IIIC treated at the Norwegian Radium Hospital (NRH) 1985-2000, in total 776, subdivided into four groups: 1) Local primary surgery, no direct re-operation at NRH, no interval debulking; 2) local primary surgery, no direct re-operation, but interval debulking after 3-4 courses of chemotherapy at NRH; 3) local primary surgery, direct re-operation at NRH, no interval debulking; 4) primary surgery at NRH. Lymph node biopsies at re-operation in early stages and upgrading of stage where necessary were registered.
Results: Whether surgery was radical or not was an independent prognostic factor for overall and progression-free survival. The treatment group was an independent prognostic factor for overall, but not for progression-free survival. Group 3 had significantly the best overall and progression-free survival (p = 0.01 and 0.05). For macroscopically radical surgery both overall and progression-free survival were found significantly better for groups 3, 4 and 1 than for group 2. Most lymph node biopsies were performed during the last period and 28% were upgraded from Stage I and II to IIIC. More patients were referred for primary surgery at NRH during the last 5-year period during which overall survival and time to progression were significantly better.
Interpretation: Whether primary surgery is radical or not is a significant prognostic factor for survival and primary surgery is best performed by specialists in gynaecological oncology.
Ovarian cancer; Treatment level; Survival
H. OKSEFJELL,B. Sandstad,C. Trope. Ovarian cancer Stage III C. Consequences of treatment level on overall and progression-free survival. European Journal of Gynaecological Oncology. 2006. 27(3);209-214.
[1] Cancer in Norway 2001. The Cancer Registry of Norway. Oslo, Norway.
[2] Pecorelli S., Benedet J.L., Creasman W.T., Stephard J.H., Petterson F.: "Annual report on the results of treatment in gynecological cancer". Vol 23. Oxford, U.K., International Federation of Gynecology and Obstetrics, 1998.
[3] BjØrge T., Engeland A., SundfØr K., Trope C.: "Prognosis of 2800patients With epithelial ovarian canser diagnosed during1975-94 and treated at the Norwegian Radium Hospital". Acta Obstet. Gynecol. Scand., 1998, 77, 777.
[4] Griffith C.T.: "Surgical resection of tumor bulk in the primary treatment of ovarian carsinoma". Natl. Cancer Inst. Monogr., 1975, 42, 101.
[5] Aure J.C., Hoeg K., Kolstad P.: "Clinical and histologic studies of ovarian carsinoma. Long-term follow-up of 990 cases". Obstet. Gynecol., 1971, 37, 1.
[6] Bristow R.E., Tomacruz R.S., Armstrong D.K., Trimble LE., Montz F.J.: "Survival effect of maximal cytoreductive surgery for advanced ovarian carcinoma during the platinum era: a meta-analysis". J. Clin. Oncol., 2002, 20, 1248.
[7] Eisenkop S.M., Spirtos N.M., Friedman R.L. et al.: "Relative influences of tumor volume before surgery and the cytoreductive outcome on survival for patients with advanced ovarian canser: a prospective study". Gynecol. Oneal., 2003, 90, 390.
[8] van der Burg M.E., van Lent M., Buyse M. et al.: "The effect of debulking surgery after induction chemoterapi on the prognosis in advanced epitelial ovarian cancer". N. Engl. J. Med., 1995, 332, 629.
[9] Berek J.S.: "Intervall debulking of epithelial ovarian cancer: an interim measure". N. Eng. J. Med., 1995, 332, 675
[10] Rose P.G., Nerenstone S., Brady M.F. et al. for GOG: "Secondary surgical cytoreduction for advanced ovarian carcinoma". N. Engl. J. Med., 2004, 531, 24.
[11] Kehoe S., Powell J., Wilson S., Woodman C.: "The influence of the operating surgeon's spesialisation on patients survival in ovarian carsnoma". Br. J. Cancer, 1994, 70, 1014.
[12] Tingulstad S., Skjeldestad F.E., Hagen B.: "The effect of centralization of primary surgery on survival in ovarian cancer patients". Obstet Gynecol., 2003, 102, 499.
[13] Junor E.J., Hole D.J., McNulty L., Mason M., Young J.: "Spesialist gynecologists and survival outcome in ovarian cancer:a Scottish National Study of 1966 patients". Br. J. Obstet. Gynecol., 1999, 106, 1130.
[14] Olaitan A., Weeks J., Mocroft A., Smith J., Howe K., Murdich J.: "The surgical management of women with ovarian cancer in the south west of England". Br. J. Cancer, 2001, 85, 1824.
[15] Gillis C.R., Hole D.J., Still R.M., Davis J., Kaye Sb.: "Medical audit, cancer registration, and survival in ovarian cancer". Lancet, 1991, 337, 611.
[16] Paulsen T., Kjærheim K., Kæm J., Tretli S., Trope C.: "Improved short-term survival for advanced ovarian, tubar and peritonal cancerpatients operated at teaching hospitals". Int. J. Gynecol. Cancer, 2006, 16 (suppl. I), 11.
[17] Goldie J.H., Coldman A.J.: "A mathematic model for relating the drug sensitivity of tumors to their spontaneous mutation rate". Cancer Treat Rep., 1979, 63, 1727.
[18] Geide K.C., Kieser K., Dodge J., Rosen B.: "Who should operate on patients with ovarian cancer? An evidence-based review". Gynecol Oneal., 2005, 99, 447.
Top