Establishment and validation of M1 stage subdivisions for de novo metastatic nasopharyngeal carcinoma to better predict prognosis and guide treatment

医学 阶段(地层学) 比例危险模型 化疗 转移 鼻咽癌 肿瘤科 前瞻性队列研究 内科学 癌 放射科 癌症 放射治疗 生物 古生物学
作者
Xiong Zou,Rui You,Huai Liu,Yu-Xiang He,Guo-Feng Xie,Zhihai Xie,Jibin Li,Rou Jiang,Li-Zhi Liu,Li Li,Meng-Xia Zhang,You-Ping Liu,Yi-Jun Hua,Ling Guo,Chao-Nan Qian,Hai-Qiang Mai,Dong-Ping Chen,Ying Luo,Liang-Fang Shen,Ming‐Huang Hong
出处
期刊:European Journal of Cancer [Elsevier BV]
卷期号:77: 117-126 被引量:135
标识
DOI:10.1016/j.ejca.2017.02.029
摘要

Abstract

Background

To better manage patients with de novo metastatic NPC (mNPC) including easily identifying individuals' survival outcomes and accurately choosing the most suitable treatment.

Materials and methods

Three independent cohorts of mNPC patients (a training set of n = 462, an internal prospective validation set of n = 272 and an external prospective validation set of n = 243) were studied. The radiological characteristics of distant metastases, including number of metastatic locations, number of metastatic lesions and size of metastatic lesions, were carefully defined based on imaging data. These three factors and other potential prognostic factors were comprehensively analysed and were further integrated into new subdivisions of stage M1 using a Cox proportional hazards model.

Results

We successfully subdivided the M1 stage into three categories: M1a, oligo metastasis without liver involvement; M1b, multiple metastases without liver involvement; and M1c, liver involvement irrespective of metastatic lesions. The 3-year overall survival ranged from 54.5% to 72.8%, from 34.3% to 41.6% and from 22.6.0%–23.6% for M1a, M1b and M1c, respectively (P < 0.001). Systemic chemotherapy combined with radical loco-regional radiotherapy may benefit patients in M1a and M1b, not in M1c. Further aggressive treatment of metastatic lesions based on systemic chemotherapy and definitive loco-regional radiotherapy showed no survival benefit, even for patients in M1a (P > 0.05).

Conclusion

The subdividing of M1 provided promising prognostic value and could aid clinicians in choosing the most suitable treatment for de novo mNPC patients.
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