Proposed modifications and incorporation of plasma Epstein-Barr virus DNA improve the TNM staging system for Epstein-Barr virus-related nasopharyngeal carcinoma.

Background: The prognosis of patients who have Epstein-Barr virus (EBV)-related nasopharyngeal carcinoma (NPC) in which the tumor tissues harbor EBV have a better prognosis than those without EBV-related NPC. Therefore, the eighth edition of the TNM staging system could be modified for EBV-related N...

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Publicado en:Cancer (0008543X) Vol. 125; no. 1; pp. 79 - 90
Autores principales: Guo, Rui, Tang, Ling‐Long, Mao, Yan‐Ping, Du, Xiao‐Jing, Chen, Lei, Zhang, Zi‐Chen, Liu, Li‐Zhi, Tian, Li, Luo, Xiao‐Tong, Xie, Yu‐Bin, Ren, Jian, Sun, Ying, Ma, Jun, Tang, Ling-Long, Mao, Yan-Ping, Du, Xiao-Jing, Zhang, Zi-Chen, Liu, Li-Zhi, Luo, Xiao-Tong, Xie, Yu-Bin
Formato: research Journal Article
Publicado: Wiley-Blackwell Jan2019
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan2019
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        133686969
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        133686969
        10.1002/cncr.31741
        NLM30351466
        133686969
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        atl: Proposed modifications and incorporation of plasma Epstein-Barr virus DNA improve the TNM staging system for Epstein-Barr virus-related nasopharyngeal carcinoma.
      aug:
        au:
          Guo, Rui
          Tang, Ling‐Long
          Mao, Yan‐Ping
          Du, Xiao‐Jing
          Chen, Lei
          Zhang, Zi‐Chen
          Liu, Li‐Zhi
          Tian, Li
          Luo, Xiao‐Tong
          Xie, Yu‐Bin
          Ren, Jian
          Sun, Ying
          Ma, Jun
          Tang, Ling-Long
          Mao, Yan-Ping
          Du, Xiao-Jing
          Zhang, Zi-Chen
          Liu, Li-Zhi
          Luo, Xiao-Tong
          Xie, Yu-Bin
        affil: Department of Radiation Oncology, Sun Yat‐sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangzhou China
      sug:
        subj:
          DNA Blood
          Epstein-Barr Virus Infections Pathology
          Epstein-Barr Virus
          Nasopharyngeal Neoplasms Pathology
          Prospective Studies
          DNA Radiation Effects
          Nasopharyngeal Neoplasms
          Male
          Nasopharyngeal Neoplasms Radiotherapy
          Radiotherapy, Conformal
          Survival Analysis
          Human
          Retrospective Design
          Female
          Epstein-Barr Virus Infections Radiotherapy
          Neoplasm Staging
          Treatment Outcomes
          Prognosis
          Epstein-Barr Virus Radiation Effects
          Validation Studies
          Comparative Studies
          Evaluation Research
          Multicenter Studies
          Funding Source
          Male
          Female
      ab: Background: The prognosis of patients who have Epstein-Barr virus (EBV)-related nasopharyngeal carcinoma (NPC) in which the tumor tissues harbor EBV have a better prognosis than those without EBV-related NPC. Therefore, the eighth edition of the TNM staging system could be modified for EBV-related NPC by incorporating the measurement of plasma EBV DNA.Methods: In total, 979 patients with NPC who received intensity-modulated radiotherapy (IMRT) were retrospectively reviewed. Recursive partitioning analysis was conducted based on tumor (T) classification, lymph node (N) classification, and EBV DNA measurement to derive objectively the proposed stage groupings. The validity of the proposed stage groupings was confirmed in a prospective cohort of 550 consecutive patients who also received with IMRT.Results: The pretreatment plasma EBV DNA level was identified as a significant, negative prognostic factor for progression-free survival and overall survival in univariate analysis (all P < .001) and multivariate analysis (all P < .05). Recursive partitioning analysis of the primary cohort to incorporate EBV DNA generated the following proposed stage groupings: stage RI (T1N0), RIIA (T2-T3N0 or T1-T3N1, EBV DNA ≤2000 copies/mL), stage RIIB (T2-T3N0 or T1-T3N1, EBV DNA >2000 copies/mL; T1-T3N2, EBV DNA ≤2000 copies/mL), stage RIII (T1-T3N2, EBV DNA >2000 copies/mL; T4N0-N2), and stage RIVA (any T and N3). In the validation cohort, the 5-year progression-free survival rate was 100%, 87.9%, 76.7%, 68.7%, and 50.4% for proposed stage RI, RIIA, RIIB, RIII, and RIV NPC, respectively (P < .001). Compared with the eighth edition TNM stage groupings, the proposed stage groupings incorporating EBV DNA provided better hazard consistency, hazard discrimination, outcome prediction, and sample size balance.Conclusions: The proposed stage groupings have better prognostic performance than the eighth edition of the TNM staging system. EBV DNA titers should be included in the TNM staging system to assess patients who have EBV-related NPC.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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