The Cumulative Cisplatin Dose Affects the Long-Term Survival Outcomes of Patients with Nasopharyngeal Carcinoma Receiving Concurrent Chemoradiotherapy

被引:25
|
作者
Peng, Hao [1 ]
Chen, Lei [1 ]
Li, Wen-Fei [1 ]
Guo, Rui [1 ]
Mao, Yan-Ping [1 ]
Zhang, Yuan [1 ]
Zhang, Fan [1 ]
Liu, Li-Zhi [2 ]
Tian, Li [2 ]
Lin, Ai-Hua [3 ]
Sun, Ying [1 ]
Ma, Jun [1 ]
机构
[1] Sun Yat Sen Univ, Dept Radiat Oncol, State Key Lab Oncol Southern China, Collaborat Innovat Ctr Canc Med,Canc Ctr, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Imaging Diag & Intervent Ctr, State Key Lab Oncol Southern China, Collaborat Innovat Ctr Canc Med,Canc Ctr, Guangzhou, Peoples R China
[3] Sun Yat Sen Univ, Dept Med Stat & Epidemiol, Sch Publ Hlth, Guangzhou, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
COMPARING NEOADJUVANT CHEMOTHERAPY; RANDOMIZED-TRIAL; PHASE-III; ADJUVANT CHEMOTHERAPY; RADIATION-THERAPY; RADIOTHERAPY; CANCER; SYSTEM; LEVEL; GAIN;
D O I
10.1038/srep24332
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
The prognostic value of the cumulative cisplatin dose (CCD) remains controversial for patients with nasopharyngeal carcinoma (NPC) receiving only concurrent chemoradiotherapy (CCRT). We retrospectively reviewed 549 consecutive patients with non-metastatic, histologically-proven NPC treated using intensity-modulated radiotherapy (IMRT) at Sun Yat-sen university cancer center. Patient survival between different CCD groups were compared. The cut-off value of pre-treatment plasma EBV DNA (pre-DNA) and CCD based on disease-free survival (DFS) were 1460 copies/ml (AUC, 0.691; sensitivity, 0.717; specificity, 0.635) and 240 mg/m(2) (AUC, 0.506; sensitivity, 0.526; specificity, 0.538), respectively. Of the entire cohort, 92/549 (16.8%) patients received a CCD >= 240 mg/m(2) and 457 (83.2%) patients, <240 mg/m(2). For CCD >= 240 mg/m(2) vs. < 240 mg/m(2), the estimated 4-year DFS, overall survival (OS), locoregional-free survival (LRFFS) and distant metastasis-free survival (DMFS) rates were 89.1% vs. 81.3% (P = 0.097), 92.4% vs. 90.0% (P = 0.369), 95.6% vs. 91.2% (P = 0.156), and 91.3% vs. 88.4% (P = 0.375), respectively. For the whole cohort, multivariate analysis identified the CCD was an independent prognostic factor for DFS (HR, 0.515; 95% CI, 0.267-0.995; P = 0.048). However, CCD (>= 240 mg/m2) had no prognostic value in subgroup analysis with stratification by the cut-off value of pre-DNA (P > 0.05 for all rates).
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页数:8
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