Progress in the management of endometrial cancer (subtypes, immunotherapy, alterations in PIK3CA pathway): data and perspectives

被引:15
|
作者
Oaknin, Ana [1 ]
Leon-Castillo, Alicia [2 ]
Lorusso, Domenica [3 ,4 ]
机构
[1] Vall dHebron Univ Hosp, Vall dHebron Inst Oncol VHIO, Med Oncol Dept, Barcelona, Spain
[2] Leiden Univ, Med Ctr, Dept Pathol, Leiden, Netherlands
[3] Fdn Policlin Univ A Gemelli IRCCS, Gynecol Oncol Unit, Rome, Italy
[4] Fdn Policlin Univ A Gemelli IRCCS, Sci Directorate, Rome, Italy
关键词
checkpoint blockade agents; endometrial cancer; mismatch repair protein status; molecular classification; phosphatidylinositol-3 kinase pathway; PHASE-II TRIAL; PI3K/AKT/MTOR PATHWAY; THERAPEUTIC TARGET; LYNCH SYNDROME; RECURRENT; CARCINOMA; CHEMOTHERAPY; TUMORS; MTOR; PI3K;
D O I
10.1097/CCO.0000000000000658
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review Changes in molecular classification together with a deeper knowledge of both immune disregulation and phosphatidylinositol-3 kinase (PI3K) pathway alterations are leading to a new endometrial cancer treatment paradigm. This review will address the cutting-edge data in this field. Recent findings This article will cover the updated data in endometrial cancer molecular classification and its correlation with the outcomes in randomized clinical trials (e.g., PORTEC-3). Moreover, we will review the latest data regarding checkpoint blockade molecules (CPB) in the recurrent setting and how they are changing the treatment landscape. In addition, the role of the PI3K inhibitors, their activity, and toxicity profile will be described. As result of the incorporation of molecular classification in our daily practice, the adjuvant treatment in endometrial cancer is rapidly evolving and leading to a new paradigm. The promising data observed with CPB in the recurrent setting have led to the food and drug administration approval of pembrolizumab as monotherapy and in combination with lenvatinib. Additionally, the current outcomes achieved with PI3K inhibitor agents encourage us to continue our clinical research to identify those patients who may benefit the most.
引用
收藏
页码:471 / 480
页数:10
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