Expression of the PI3K/AKT/mTOR pathway as a prognostic factor in patients with advanced high grade serous ovarian carcinoma treated with neoadjuvant chemotherapy

被引:3
|
作者
Cierniak, S. [1 ]
Koktysz, R. [1 ]
Jesiotr, M. [1 ]
Gasowska-Bodnar, A. [2 ]
Bodnar, L. [3 ]
机构
[1] Mil Inst Med, Dept Pathol, Warsaw, Poland
[2] Mil Inst Med, Dept Gynecol & Gynecol Oncol, Warsaw, Poland
[3] Mil Inst Med, Dept Oncol, 128 Szaserow Str, PL-04141 Warsaw, Poland
关键词
High grade serous ovarian carcinoma; PI3K/AKT/mTOR pathway; Neoadjuvant chemotherapy; MTOR PATHWAY; PTEN; SURVIVAL;
D O I
10.12892/ejgo4575.2019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The aim of this study was to search biomarkers in patients with high grade serous ovarian carcinoma (HGSOC) treated with neoadjuvant chemotherapy (NACT) among the components of PI3K/AKT/mTOR pathway. Material and Methods: The authors assessed 49 patients with HGSOC (FIGO IIIC-IV) treated with NACT. The expression of PI3KCA, PTEN, pAKT473, mTOR, and p70S6K were assessed immunohistochemically. Results: The expression of PI3KCA and p70S6K in tumour tissue after NACT was significantly decreased compared to before chemotherapy (p = 0.0005 and p = 0.0256, respectively). Multivariate analysis demonstrated that high mTOR expression, suboptimal range of interval debulking surgery (IDS), platinum resistance, and the lack of paclitaxel in the NACT were independent adverse prognostic factors (HR=3.86, 95% CI (1.75-8.56); HR = 3.94, 95% CI (1.76-8.83); HR = 2.29, 95% CI (1.13-4.64); and HR- 4.76, 95% CI (1.80-12.59),p < 0.05). Conclusions: The mTOR expression may be an independent prognostic factor, but further investigations are needed.
引用
收藏
页码:744 / 751
页数:8
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