The addition of pretreatment plasma Epstein-Barr virus DNA into the eighth edition of nasopharyngeal cancer TNM stage classification

被引:73
|
作者
Lee, Victor Ho-Fun [1 ,2 ]
Kwong, Dora Lai-Wan [1 ,2 ]
Leung, To-Wai [1 ]
Choi, Cheuk-Wai [1 ]
O'Sullivan, Brian [2 ,3 ]
Lam, Ka-On [1 ,2 ]
Lai, Vincent [4 ]
Khong, Pek-Lan [4 ]
Chan, Sik-Kwan [1 ]
Ng, Chor-Yi [1 ]
Tong, Chi-Chung [1 ]
Ho, Patty Pui-Ying [1 ]
Chan, Wing-Lok [1 ]
Wong, Lai-San [1 ]
Leung, Dennis Kwok-Chuen [1 ]
Chan, Sum-Yin [1 ]
So, Tsz-Him [1 ]
Luk, Mai-Yee [1 ]
Lee, Anne Wing-Mui [1 ,2 ]
机构
[1] Univ Hong Kong, Li Ka Shing Fac Med, Dept Clin Oncol, Hong Kong, Peoples R China
[2] Univ Hong Kong, Clin Oncol Ctr, Shenzhen Hosp, Shenzhen, Peoples R China
[3] Univ Toronto, Dept Radiat Oncol, Princess Margaret Canc Ctr, Toronto, ON, Canada
[4] Univ Hong Kong, Li Ka Shing Fac Med, Dept Diagnost Radiol, Hong Kong, Peoples R China
关键词
nasopharyngeal carcinoma; plasma EBV DNA; stage classification; recursive partitioning analysis; survival prediction; MODULATED RADIATION-THERAPY; INTERNATIONAL COLLABORATION; CARCINOMA; RADIOTHERAPY; SYSTEM; PROGNOSTICATION; LOAD; ERA;
D O I
10.1002/ijc.31856
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The eighth edition of the American Joint Committee on Cancer (AJCC)/Union for International Cancer Control (UICC) stage classification (TNM) for nasopharyngeal carcinoma (NPC) was launched. It remains unknown if incorporation of nonanatomic factors into the stage classification would better predict survival. We prospectively recruited 518 patients with nonmetastatic NPC treated with radical intensity-modulated radiation therapy +/- chemotherapy based on the eighth edition TNM. Recursive partitioning analysis (RPA) incorporating pretreatment plasma Epstein-Barr virus (EBV) DNA derived new stage groups. Multivariable analyses to calculate adjusted hazard ratios (AHRs) derived another set of stage groups. Five-year progression-free survival (PFS), overall survival (OS) and cancer-specific survival (CSS) were: Stage I (PFS 100%, OS 90%, CSS 100%), II (PFS 88%, OS 84%, CSS 95%), III (PFS 84%, OS 84%, CSS 90%) and IVA (PFS 71%, OS 75%, CSS 80%) (p < 0.001, p = 0.066 and p = 0.002, respectively). RPA derived four new stages: RPA-I (T1-T4 N0-N2 & EBV DNA <500 copies per mL; PFS 94%, OS 89%, CSS 96%), RPA-II (T1-T4 N0-N2 & EBV DNA >= 500 copies per mL; PFS 80%, OS 83%, CSS 89%), RPA-III (T1-T2 N3; PFS 64%, OS 83%, CSS 83%) and RPA-IVA (T3-T4 N3; PFS 63%, OS 60% and CSS 68%) (all with p < 0.001). AHR using covariate adjustment also yielded a valid classification (I: T1-T2 N0-N2; II: T3-T4 N0-N2 or T1-T2 N3 and III: T3-T4 N3) (all with p < 0.001). However, RPA stages better predicted survival for PS and CSS after bootstrapping replications. Our RPA-based stage groups revealed better survival prediction compared to the eighth edition TNM and the AHR stage groups.
引用
收藏
页码:1713 / 1722
页数:10
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