4.5 Article

Combination of Tumor Volume and Epstein-Barr Virus DNA Improved Prognostic Stratification of Stage II Nasopharyngeal Carcinoma in the Intensity Modulated Radiotherapy Era: A Large-Scale Cohort Study

期刊

CANCER RESEARCH AND TREATMENT
卷 50, 期 3, 页码 861-871

出版社

KOREAN CANCER ASSOCIATION
DOI: 10.4143/crt.2017.237

关键词

Nasopharyngeal carcinoma; Tumor burden; Epstein-Barr virus; Intensity modulated radiotherapy; Prognosis

类别

资金

  1. Ministry of Science and Technology of China [2011CB504300]
  2. National Natural Science Foundation of China [81025014, 81230045, 81201629, 91019015, 81071932, 30600755, 81072226]
  3. 863 Project [2012AA02A501]
  4. National Key Basic Research Program of China [2013CB910304]
  5. Sci-Tech Project Foundation of Guangdong Province [2011B080701034, 2011B031800161]
  6. Sci-Tech Project Foundation of Guangzhou City [2011J4300100]
  7. Sun Yat-sen University Clinical Research 5010 Program
  8. Sun Yat-sen University Cancer Center Clinical Research 308 Program
  9. Fundamental Research Funds for the Central Universities

向作者/读者索取更多资源

Purpose Little is known about combination of the circulating Epstein-Barr viral (EBV) DNA and tumor volume in prognosis of stage II nasopharyngeal carcinoma (NPC) patients in the intensity modulated radiotherapy (IMRT) era. We conducted this cohort study to evaluate the prognostic values of combining these two factors. Materials and Methods By Kaplan-Meier, we compare the differences of survival curves between 385 patients with different EBV DNA or tumor volume levels, or with the combination of two biomarkers mentioned above. Results Gross tumor volume of cervical lymph nodes (GTVnd, p < 0.001) and total tumor volume (GTVtotal, p < 0.001) were both closely related to pretreatment EBV DNA, while gross tumor volume of nasopharynx (GTVnx, p=0.047) was weakly related to EBV DNA. EBV DNA was significantly correlated with progress-free survival (PFS, p=0.005), locoregional-free survival (LRFS, p=0.039), and distant metastasis-free survival (DMFS, p=0.017), while GTVtotal, regardless of GTVnx and GTVnd, had a significant correlation with PFS and LRFS. The p-values of GTVtotal for PFS and LRFS were 0.008 and 0.001, respectively. According to GTVtotal and pretreatment EBV DNA level, patients were divided into a low-risk group (EBV DNA 0 copy/mL, GTVtotal < 30 cm(3); EBV DNA 0 copy/mL, GTVtotal. 30 cm(3); or EBV DNA > 0 copy/mL, GTVtotal < 30 cm(3)) and a high-risk group (EBV DNA > 0 copy/mL, GTVtotal. 30 cm(3)). When patients in the low-risk group were compared with those in the high-risk group, 3-year PFS (p=0.003), LRFS (p=0.010), and DMFS (p=0.031) rates were statistically significant. Conclusion Pretreatment plasma EBV DNA and tumor volume were both closely correlated with prognosis of stage II NPC patients in the IMRT era. Combination of EBV DNA and tumor volume can refine prognosis and indicate for clinical therapy.

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