A new prognostic model comprising p53, EGFR, and tumor grade in early stage epithelial ovarian carcinoma and avoiding the problem of inaccurate surgical staging

2004 ◽  
Vol 14 (2) ◽  
pp. 259-270 ◽  
Author(s):  
I. Skirnisdottir ◽  
T. Seidal ◽  
B. Sorbe
Author(s):  
Renée E.W.M. van de Vorst ◽  
Jacob P. Hoogendam ◽  
Maaike A. van der Aa ◽  
Petronella O. Witteveen ◽  
Ronald P. Zweemer ◽  
...  

Author(s):  
Shu-Feng Hsieh ◽  
Hei-Yu Lau ◽  
Hua-Hsi Wu ◽  
Heng-Cheng Hsu ◽  
Nae-Fang Twu ◽  
...  

We aimed to determine prognostic factors of early stage (I/II) epithelial ovarian carcinoma (EOC) including clinicopathologic and chemotherapeutic regimens. Four hundred and thirty-seven women who underwent primary staging surgery with adjuvant chemotherapy between January 1, 2000 and December 31, 2010 were retrospectively reviewed and analyzed from two medical centers. The prognostic factors were determined from multivariate survival analyses using Cox regression models. The majority of women were diagnosed with stage Ic (244/437, 55.8%). The histopathologic types were clear cell (37.5%), endometrioid (27.2%), serous (14.0%), and mucinous (13.3%). Fifty-seven percent (249/437) of the women received taxane-based (platinum plus paclitaxel) regimens and 43.0% received non-taxane (platinum plus cyclophosphamide) regimens as frontline adjuvant chemotherapy. Clear cell tumors (adjusted Hazard ratio (aHR) 0.37, 95% confidence interval (CI) 0.21–0.73, p = 0.001) showed better 5-year disease-free survival (DFS) than serous tumors. Women diagnosed at FIGO (International Federation of Gynecology and Obstetrics) stage II (aHR 5.97, 95% CI = 2.47–14.39, p < 0.001), grade 3 tumor without clear cell (aHR 2.28, 95% CI = 1.02–5.07, p = 0.004) and who received 3–5 cycles of non-taxane regimens (aHR 3.29, 95% CI = 1.47–7.34, p = 0.004) had worse 5-year overall survival (OS). Clear cell histology treated with taxane-based regimens showed significantly higher 5-year DFS (91.2% vs. 82.0%, aHR = 0.45, 95% CI = 0.21–0.93, p = 0.043) and 5-year OS (93.5% vs. 79.0%, aHR = 0.30, 95% CI = 0.13–0.70, p = 0.005) than those treated with non-taxane-based regimens. We conclude that stage, tumor grade, and chemotherapeutic regimens/cycles are independent prognostic factors for early stage ovarian cancer.


Author(s):  
Renée van de Vorst ◽  
Jacob Hoogendam ◽  
Maaike van der Aa ◽  
Petronella Oda Witteveen ◽  
Ronald Zweemer ◽  
...  

Background: Tumor positivity and upstaging rates from various surgical staging components performed in clinically early-stage epithelial ovarian carcinoma (EOC) vary widely in literature. Objectives: To quantify tumor positivity and upstaging rates for all staging surgery components in EOC patients. Differences between subgroups based on their clinical and histological characteristics are explored. Search strategy: A systematic search using synonyms of ‘ovarian cancer’, ‘neoplasm staging’, and ’neoplasm metastasis’ was conducted in PubMed, Embase, and the Cochrane Library. Selection criteria: Meta-analysis was performed on 23 included studies, comprising 5194 clinical stage I or II EOC patients who underwent comprehensive surgical staging. Data Collection and Analysis: Studies were assessed using the Newcastle-Ottawa Scale risk-of-bias tool. Pooled proportions and 95% confidence intervals were calculated using an inverse variance weighted random-effects model. Main Results: Overall upstaging rate of clinically early-stage EOC patients was 18.7% (95%CI: 14.1-23.4%). Serous histology or high grade EOC showed the highest upstaging rate at 35.3% (95%CI: 21.8-48.7%) and 40.9% (95%CI: 35.6-46.2%). Lymph node involvement resulted in an upstaging rate of 8.7% (95%CI: 6.2-11.3%). Tumor was identified in uterus, cytology, peritoneal biopsies, omentum and appendix in 6.2% (95%CI: 1.8-10.7%), 18.4% (95%CI: 13.8-22.9%), 9.7% (95%CI: 3.8-15.6%), 5.2% (95%CI: 1.7-8.8%) and 3.6% (95%CI: 0.0-7.5%) of EOC patients. The corresponding upstaging rates were 5.9% (95%CI: 1.4-10.4%), 8.5% (95%CI: 1.8-15.2%), 3.5% (95%CI: 1.0-6.0%), 3.9% (95%CI: 1.4-6.3%) and 1.6% (95%CI: 0.0-3.4%), respectively. Conclusion: The attributive value of comprehensive surgical staging in clinically early-stage EOC patients remains substantial, particularly in serous and high grade tumors.


2019 ◽  
Vol 154 (2) ◽  
pp. 308-313 ◽  
Author(s):  
E.M. Hengeveld ◽  
P.L.M. Zusterzeel ◽  
H. Lajer ◽  
C.K. Høgdall ◽  
M. Rosendahl

2002 ◽  
Vol 85 (2) ◽  
pp. 351-355 ◽  
Author(s):  
Tien Le ◽  
Allyson Adolph ◽  
G.V. Krepart ◽  
R. Lotocki ◽  
M.S. Heywood

2005 ◽  
Vol 23 (16_suppl) ◽  
pp. 5167-5167 ◽  
Author(s):  
J. A. García-Saénz ◽  
A. Casado ◽  
J. Puente ◽  
S. López-Tarruella ◽  
J. C. Camara ◽  
...  

1999 ◽  
Vol 74 (2) ◽  
pp. 252-254 ◽  
Author(s):  
T. Le ◽  
G.V. Krepart ◽  
R.J. Lotocki ◽  
M.S. Heywood

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