Endometrioid Endometrial RNA Index Predicts Recurrence in Stage I Patients

被引:1
|
作者
Nief, Corrine A. [1 ,2 ]
Hammer, Phoebe M. [2 ]
Wang, Aihui [2 ]
Charu, Vivek [2 ]
Tanweer, Amina [2 ]
Litkouhi, Babak [4 ]
Kidd, Elizabeth [5 ]
Gentles, Andrew J. [2 ,3 ]
Howitt, Brooke E. [2 ]
机构
[1] Stanford Univ, Sch Med, Stanford, CA USA
[2] Stanford Univ, Dept Pathol, 300 Pasteur Dr,L235, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Gynecol Oncol, Stanford, CA USA
[4] Stanford Univ, Dept Biomed Data Sci, Stanford, CA USA
[5] Stanford Univ, Dept Radiat Oncol, Stanford, CA USA
关键词
CANCER; RISK; CLASSIFICATION;
D O I
10.1158/1078-0432.CCR-23-3158
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Risk prediction with genomic and transcriptomic data has the potential to improve patient outcomes by enabling clinicians to identify patients requiring adjuvant treatment approaches, while sparing low-risk patients from unnecessary interventions. Endometrioid endometrial carcinoma (EEC) is the most common cancer in women in developed countries, and rates of endometrial cancer are increasing. Experimental Design: We collected a 105-patient case-control cohort of stage I EEC comprising 45 patients who experienced recurrence less than 6 years after excision, and 60 F & eacute;d & eacute;ration Internationale de Gyn & eacute;cologie et d'Obst & eacute;trique grade-matched controls without recurrence. We first utilized two RNA-based, previously validated machine learning approaches, namely, EcoTyper and Complexity Index in Sarcoma (CINSARC). We developed Endometrioid Endometrial RNA Index (EERI), which uses RNA expression data from 46 genes to generate a personalized risk score for each patient. EERI was trained on our 105-patient cohort and tested on a publicly available cohort of 263 patients with stage I EEC. Results: EERI was able to predict recurrences with 94% accuracy in the training set and 81% accuracy in the test set. In the test set, patients assigned as EERI high-risk were significantly more likely to experience recurrence (30%) than the EERI low-risk group (1%) with a hazard ratio of 9.9 (95% CI, 4.1-23.8; P < 0.001). Conclusions: Tumors with high-risk genetic features may require additional treatment or closer monitoring and are not readily identified using traditional clinicopathologic and molecular features. EERI performs with high sensitivity and modest specificity, which may benefit from further optimization and validation in larger independent cohorts.
引用
收藏
页码:2801 / 2811
页数:11
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