A new clinical-genomic model to predict 10-year recurrence risk in primary operable breast cancer patients

被引:11
|
作者
Huang, Tzu-Ting [1 ]
Lei, Lei [2 ,3 ]
Chen, Ching-Hsuan Andre [4 ]
Lu, Tzu-Pin [4 ]
Jen, Chung-Wen [5 ]
Cheng, Skye Hung-Chun [5 ,6 ]
机构
[1] Koo Fdn, Sun Yat Sen Canc Ctr, Dept Res, Taipei, Taiwan
[2] Univ Chinese Acad Sci, Zhejiang Canc Hosp, Canc Hosp, Dept Breast Med Oncol, Hangzhou, Zhejiang, Peoples R China
[3] Univ Mississippi, Med Ctr, Jackson, MS 39216 USA
[4] Natl Taiwan Univ, Dept Publ Hlth, Epidemiol & Prevent Med, Taipei, Taiwan
[5] Koo Fdn, Sun Yat Sen Canc Ctr, Dept Radiat Oncol, Taipei, Taiwan
[6] Taitung Christian Hosp, Dept Radiat Oncol, Taitung Canc Ctr, Taitung, Taiwan
关键词
LOCOREGIONAL RECURRENCE; MASTECTOMY; SIGNATURES; STAGE;
D O I
10.1038/s41598-020-61535-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study aimed to validate the long-term prognostic value of a new clinical-genomic model, Distant Genetic Model-Clinical Variable Model 6 (DGM-CM6), developed in Asia as a prognostic panel for all subtypes of breast cancer. We included 752 operable stage I-III breast cancer patients representing all subtypes treated from 2005 to 2014 as the validation cohort. The median follow-up was 95.8 months. The low- and high-risk patients classified by DGM-CM6 (RI-DR) had significant differences in 10-year distant recurrence-free interval (DRFI) (94.1% vs. 85.0%, P < 0.0001) and relapse-free survival (RFS) (90.0% vs. 80.5%, P = 0.0003). External validation using EMTAB-365 dataset showed similar observation (P < 0.0001). DGM-CM6 was an independent prognostic factor by multivariate analysis with hazard ratios of 3.1 (1.6-6.0) for RFS (P = 0.0009) and 3.8 (1.6-9.0) for DRFI (P = 0.0028). Comparing the C-index of DGM-CM6 and PAM50-ROR scores, the former performed better than the latter in predicting long-term DRFI and RFS, especially in N0, ER/PR-positive, and HER2-negative patients.
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页数:10
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