4.8 Article

Liquid biopsy tracking during sequential chemo-radiotherapy identifies distinct prognostic phenotypes in nasopharyngeal carcinoma

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NATURE COMMUNICATIONS
卷 10, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-11853-y

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资金

  1. Pearl River Scholar Funded Scheme
  2. Special Support Program of Sun Yat-sen University Cancer Center [16zxtzlc06]
  3. Health & Medical Collaborative Innovation Project of Guangzhou City, China [201803040003, 201604020003]
  4. Natural Science Foundation of Guang Dong Province [2017A030312003]
  5. Innovation Team Development Plan of the Ministry of Education [IRT_17R110]
  6. Overseas Expertise Introduction Project for Discipline Innovation (111 Project) [B14035]
  7. National Natural Science Foundation of China [81802707]
  8. National Medical Research Council Singapore Clinician-Scientist Award [NMRC/CSA/0027/2018]
  9. Duke-NUS Oncology Academic Program Proton Research Program
  10. National Research Foundation [NRF-CRP17-2017-05]

向作者/读者索取更多资源

Liquid biopsies have the utility for detecting minimal residual disease in several cancer types. Here, we investigate if liquid biopsy tracking on-treatment informs on tumour phenotypes by longitudinally quantifying circulating Epstein-barr virus (EBV) DNA copy number in 673 nasopharyngeal carcinoma patients undergoing radical induction chemotherapy (IC) and chemo-radiotherapy (CRT). We observe significant inter-patient heterogeneity in viral copy number clearance that is classifiable into eight distinct patterns based on clearance kinetics and bounce occurrence, including a substantial proportion of complete responders (approximate to 30%) to only one IC cycle. Using a supervised statistical clustering of disease relapse risks, we further bin these eight subgroups into four prognostic phenotypes (early responders, intermediate responders, late responders, and treatment resistant) that are correlated with efficacy of chemotherapy intensity. Taken together, we show that real-time monitoring of liquid biopsy response adds prognostic information, and has the potential utility for risk-adapted treatment de-intensification/intensification in nasopharyngeal carcinoma.

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