Back to Search Start Over

Impact of lower uterine segment involvement in type II endometrial cancer and the unique mutational profile of serous tumors.

Authors :
Kogan L
Octeau D
Amajoud Z
Abitbol J
Laskov I
Ferenczy A
Pelmus M
Eisenberg N
Kessous R
Lau S
Yasmeen A
Gotlieb WH
Salvador S
Source :
Gynecologic oncology reports [Gynecol Oncol Rep] 2018 Mar 19; Vol. 24, pp. 43-47. Date of Electronic Publication: 2018 Mar 19 (Print Publication: 2018).
Publication Year :
2018

Abstract

Objective: Evaluation of the impact of lower uterine segment involvement (LUSI) in type II endometrial cancer, and mutational profile of uterine papillary serous carcinomas (UPSC).<br />Methods: Retrospective cohort study comparing patients with type II endometrial cancer with LUSI to patients without LUSI. Genes commonly implicated in carcinogenesis were analyzed in a subgroup of 42 patients with UPSC using next generation sequencing.<br />Results: 83 patients with type II endometrial cancer were included in the study, of these, LUSI was diagnosed in 31.3%. During a median follow-up of 45.5 months, patients with LUSI developed more local and distant recurrences (local: 19.2% vs. 3.5%, P  = .03; distant: 50% vs. 17.5%, P  = .004) and progression events (73.1% vs. 26.3%, P  < .001), with shorter mean progression-free survival (16 months compared to 26.5 months, P  < .01). In a multivariate analysis, LUSI was the only significant pathological factor, associated with a 2.9-fold increase in the risk of progression ( P  = .007), and a 2.6-fold increase in the risk of death ( P  = .02). In the subgroup of patients with UPSC, mutations were identified in 54 genes, including TP53 (80%), PPP2R1A (40%), and PTEN (22.5%). Frequent mutations in the PTEN-PI3K-AKT signaling pathway were found in patients with tumor in the upper uterine segment only ( P  = .04), with PTEN being mutated in 29% of the samples ( P  = .07).<br />Conclusion: Type II endometrial cancers presenting in the LUS have a significantly worse prognosis and this might be associated with a unique mutational profile.

Details

Language :
English
ISSN :
2352-5789
Volume :
24
Database :
MEDLINE
Journal :
Gynecologic oncology reports
Publication Type :
Academic Journal
Accession number :
29915797
Full Text :
https://doi.org/10.1016/j.gore.2018.03.004