Endometrial cancer: Predictive models and clinical impact

被引:11
作者
Bendifallah, Sofiane [1 ]
Ballester, Marcos [1 ,2 ]
Darai, Emile [1 ,2 ]
机构
[1] Univ Pierre & Marie Curie Paris 6, Hop Tenon, AP HP, Serv Gynecol Obstet & Med Reprod, 4 Rue Chine, F-75020 Paris, France
[2] Univ Pierre & Marie Curie Paris 6, INSERM, UMR S 938, F-75012 Paris, France
关键词
Endometrial cancer; Predictive modeling; Lymph node metastase; Recurrence; LYMPH-NODE METASTASIS; EXTERNAL VALIDATION; SCORING SYSTEM; HIGH-RISK; RANDOMIZED-TRIAL; NOMOGRAM; CARCINOMA; SURVIVAL; RADIOTHERAPY; MULTICENTER;
D O I
10.1016/j.bulcan.2017.06.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In France, in 2015, endometrial cancer (CE) is the first gynecological cancer in terms of incidence and the fourth cause of cancer of the woman. About 8151 new cases and nearly 2179 deaths have been reported. Treatments (surgery, external radiotherapy, brachytherapy and chemotherapy) are currently delivered on the basis of an estimation of the recurrence risk, an estimation of lymph node metastasis or an estimate of survival probability. This risk is determined on the basis of prognostic factors (clinical, histological, imaging, biological) taken alone or grouped together in the form of classification systems, which are currently insufficient to account for the evolutionary and prognostic heterogeneity of endometrial cancer. For endometrial cancer, the concept of mathematical modeling and its application to prediction have developed in recent years. These biomathematical tools have opened a new era of care oriented towards the promotion of targeted therapies and personalized treatments. Many predictive models have been published to estimate the risk of recurrence and lymph node metastasis, but a tiny fraction of them is sufficiently relevant and of clinical utility. The optimization tracks are multiple and varied, suggesting the possibility in the near future of a place for these mathematical models. The development of high-throughput genomics is likely to offer a more detailed molecular characterization of the disease and its heterogeneity.
引用
收藏
页码:1022 / 1031
页数:10
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