4.6 Article

Identifying optimal candidates for local treatment of the primary tumor among patients with de novo metastatic nasopharyngeal carcinoma: a retrospective cohort study based on Epstein-Barr virus DNA level and tumor response to palliative chemotherapy

Journal

BMC CANCER
Volume 19, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12885-019-5281-5

Keywords

Metastatic nasopharyngeal carcinoma; Epstein-Barr virus DNA; Tumor response; Local treatment; Radiotherapy; Survival

Categories

Funding

  1. National Key R&D Program of China [2016YFC0902003, 2017YFC1309003, 2017YFC0908500]
  2. National Natural Science Foundation of China [81425018, 81672868, 81602371]
  3. Sun Yat-sen University Clinical Research 5010 Program [201707020039, 2014A020212103, 16zxyc02]
  4. Sci-Tech Project Foundation of Guangzhou City [201707020039]
  5. National Key Basic Research Program of China [2013CB910304]
  6. Special Support Plan of Guangdong Province [2014TX01R145]
  7. Sci-Tech Project Foundation of Guangdong Province [2014A020212103]
  8. Health & Medical Collaborative Innovation Project of Guangzhou City [201400000001]
  9. National Science & Technology Pillar Program [2014BAI09B10]
  10. Natural Science Foundation of Guangdong Province, China [2016A030310221]
  11. cultivation foundation for the junior teachers in Sun Yat Sen University [16ykpy28]
  12. Fundamental Research Funds for the Central Universities
  13. foundation for major project and new cross subject in Sun Yat Sen University [16ykjc38]

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To evaluate the clinical outcome in patients with de novo metastatic nasopharyngeal carcinoma (NPC) treated or not treated with locoregional radiotherapy (LRRT) based on plasma Epstein-Barr virus (EBV) DNA level and tumor response after palliative chemotherapy (PCT). From 2007 to 2016, 502 patients with de novo metastatic NPC were included in this study. All patients were treated with PCT and 315 patients received LRRT. Our primary study endpoint was overall survival (OS). EBV DNA was detected in 461 patients (91.8%) before treatment but was undetectable in 249 patients (49.6%) after PCT. Three hundred and seventeen patients (63.1%) achieved satisfactory response (complete response or partial response) to PCT. Both the post-PCT EBV DNA level and tumor response were independent prognostic factors. Among low-risk patients (patients with undetectable EBV DNA and satisfactory tumor response after PCT), the 3-year OS rate was 80.4% in LRRT-treated patients and 45.3% in patients not treated with LRRT (P < 0.001). Multivariate analyses demonstrated that LRRT was an independent prognostic factor of OS in the low-risk patients (P < 0.001). However, among the high-risk patients (patients with detectable EBV DNA and/or unsatisfactory response after PCT), no statistically significant survival differences were observed between the LRRT and non-LRRT groups. EBV DNA level and tumor response after PCT both correlate with the prognosis of de novo metastatic NPC. In such cases, LRRT may benefit the patients with undetectable EBV DNA levels and satisfactory tumor response after PCT.

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