scholarly journals Immunoexpression and prognostic role of p53 in different subtypes of epithelial ovarian carcinoma

2012 ◽  
Vol 26 (4) ◽  
Author(s):  
Lihong Chen ◽  
Lianxiang Li ◽  
Feng Chen ◽  
Dalin He
Oncogene ◽  
2016 ◽  
Vol 36 (21) ◽  
pp. 3025-3036 ◽  
Author(s):  
H Gurler Main ◽  
J Xie ◽  
G G Muralidhar ◽  
O Elfituri ◽  
H Xu ◽  
...  

Neoplasma ◽  
2010 ◽  
Vol 57 (6) ◽  
pp. 545-551 ◽  
Author(s):  
L. ZHANG ◽  
C. PENG ◽  
J. PENG ◽  
L. JIANG ◽  
M. NING ◽  
...  

2012 ◽  
Vol 18 (25) ◽  
pp. 3812-3815 ◽  
Author(s):  
Danijela Jelovac ◽  
Deborah K. Armstrong

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Marina Bagnoli ◽  
Giovanni L. Beretta ◽  
Laura Gatti ◽  
Silvana Pilotti ◽  
Paola Alberti ◽  
...  

Ovarian cancer is the main cause of death from gynaecological malignancies. In spite of the efficacy of platinum-paclitaxel treatment in patients with primary epithelial ovarian carcinoma, platinum-based chemotherapy is not curative and resistance remains one of the most important causes of treatment failure. Although ABC transporters have been implicated in cellular resistance to multiple drugs, the clinical relevance of these efflux pumps is still poorly understood. Thus, we examined the prognostic role of transporters of the MRP family (i.e., ABCC1/MRP1, ABCC4/MRP4) to gain insights into their clinical impacts. A case material of 127 patients with ovarian carcinoma at different stages and histotypes was used. The expression of MRP1 and MRP4 was examined by immunohistochemistry using tissue microarrays in tumor specimens collected at the time of initial surgery expression. We found an association between MRP1 expression and grading, and we observed that MRP4 displayed an unfavourable impact on disease relapse in multivariate analysis (HR = 2.05, 95% CI: 1.01–4.11;P=0.045). These results suggest that in epithelial ovarian cancer, MRP1 may be a marker for aggressiveness because its expression was associated with tumor grade and support that MRP4 may play an unfavourable role in disease outcome.


2017 ◽  
Vol 27 (4) ◽  
pp. 708-713 ◽  
Author(s):  
Edwina Coghlan ◽  
Tarek M. Meniawy ◽  
Aime Munro ◽  
Max Bulsara ◽  
Colin JR Stewart ◽  
...  

ObjectiveOur objective was to validate the prognostic role of the chemotherapy response score (CRS), which has been proposed for measuring tumor response to neoadjuvant chemotherapy in patients with high-grade serous tubo-ovarian carcinoma, in predicting progression-free survival (PFS) and overall survival (OS).MethodsA retrospective cohort study was conducted of patients with advanced high-grade serous tubo-ovarian carcinoma diagnosed between January 1, 2010, and December 31, 2014, and treated with neoadjuvant chemotherapy. Treatment-related tumor regression was determined according to the 3-tier CRS, and results were compared with standard clinicopathological variables. Survival analysis was performed using Cox proportional hazards models and the log-rank test.ResultsSeventy-one patients were eligible for analysis. Median OS was 25.5 months. Fifty-eight patients (82%) had disease recurrence and 32 (45%) had died at study census. Of the 71 patients, 19, 29, and 23 patients had a CRS of 1, 2, and 3, respectively. On univariate analysis, the CRS significantly predicted PFS (hazard ratio [HR], 3.77; 95% confidence interval [CI], 1.83–7.78; P = 0.000) and OS (HR, 2.81; 95% CI, 1.16–6.79; P = 0.022). In a multivariate model, the CRS was significantly associated with PFS (HR, 2.81; 95% CI, 1.16–6.79; P = 0.022) but not with OS (HR, 2.39; 95% CI, 0.47–3.08; P = 0.079). Patients with CRS of 1 and 2 combined were twice as likely to progress during the study period compared with patients with a CRS of 3 (HR, 2.0; 95% CI, 1.06–3.78; P = 0.032; median PFS, 16 vs 26 months). No significant association was observed for OS (CRS 1/2 vs 3; HR, 1.57; 95% CI, 0.68–3.65; P = 0.291).ConclusionsIn this study, the CRS showed independent prognostic significance for PFS but not for OS.


Sign in / Sign up

Export Citation Format

Share Document