Molecular classification defines outcomes and opportunities in young women with endometrial carcinoma

被引:101
作者
Britton, Heidi [1 ]
Huang, Leo [2 ]
Lum, Amy [2 ]
Leung, Samuel [2 ]
Shum, Kathryn [2 ]
Kale, Mruganka [1 ]
Burleigh, Angela [1 ]
Senz, Janine [2 ]
Yang, Winnie [2 ]
McConechy, Melissa [3 ]
Kommoss, Stefan [4 ]
Brucker, Sara [4 ]
Talhouk, Aline [5 ,6 ]
Gilks, C. Blake [2 ]
McAlpine, Jessica N. [7 ]
机构
[1] Univ British Columbia, Fac Med, Vancouver, BC, Canada
[2] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC, Canada
[3] Univ British Columbia, Contextual Genom Inc, Vancouver, BC, Canada
[4] Tubingen Univ Hosp, Dept Gynecol & Obstet, Div Gynecol Oncol, Tubingen, Germany
[5] Univ British Columbia, Dept Gynecol & Obstet, Vancouver, BC, Canada
[6] Univ British Columbia, Dept Stat, Vancouver, BC, Canada
[7] Univ British Columbia, Dept Gynecol & Obstet, Div Gynecol Oncol, Vancouver, BC, Canada
基金
加拿大健康研究院;
关键词
Endometrial cancer; Molecular classification; Young women; POLE; Lynch; Mismatch repair; FERTILITY-SPARING-MANAGEMENT; REPRODUCTIVE OUTCOMES; CANCER STATISTICS; RISK; ADENOCARCINOMA; MUTATIONS; PRESERVATION; OOPHORECTOMY; HYPERPLASIA; MORTALITY;
D O I
10.1016/j.ygyno.2019.03.098
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. Approximately 15% of endometrial carcinomas (ECs) arise in young women who may wish to avoid surgical menopause and/or preserve fertility. Our aim was to evaluate the prognostic significance of Proactive Molecular risk classifier for Endometrial Carcinoma (ProMisE) in young (<50 yo) women with EC. Methods. ProMisE was applied to a retrospective cohort of women with ECs <50 yo at diagnosis, and associations between the four ProMisE molecular subtypes (MMR deficient (MMRd), POLE mutated (POLE), p53 wild type (p53wt), and p53 abnormal (p53abn)) and clinicopathological parameters, including outcomes, were assessed. Results. Of 257 ECs, there were 48 (19%) MMRd, 34 (13%) POLE, 164 (64%) p53wt and 11 (4%) p53abn. ProMisE subtypes were associated with differences in all measured clinicopathological parameters except for presence of synchronous ovarian tumours and fertility. Age at diagnosis was youngest and BMI highest in women with p53wt ECs. MMRd and p53abn tumours were more likely to be advanced stage (III/IV), high-risk (ESMO), and receive chemotherapy. ProMisE subtypes were strongly associated with outcomes (overall, disease-specific, and progression-free survival (p < 0.0001 for all)). Advanced stage, grade, LVSI, myometrial invasion and ESMO risk groups showed associations with some but not all survival parameters. ProMisE maintained a strong association with OS and DSS on multivariable analysis. Conclusions. ProMisE molecular classification is prognostic in young women with EC, enabling early stratification and risk assignment to direct care. Further studies can assess response to therapy, fertility, and cancer-related outcomes within the framework of molecular subtype. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:487 / 495
页数:9
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