Prospective evaluation of plasma Epstein-Barr virus DNA clearance and fluorodeoxyglucose positron emission scan in assessing early response to chemotherapy in patients with advanced or recurrent nasopharyngeal carcinoma

被引:19
|
作者
Ma, Brigette [1 ,2 ]
Hui, Edwin P. [1 ,2 ]
King, Ann [3 ]
Leung, Sing F. [1 ,2 ]
Kam, Michael K. M. [1 ,2 ]
Mo, Frankie [1 ,2 ]
Li, Leung [1 ,2 ]
Wang, Ki [3 ]
Loong, Herbert [3 ]
Wong, Ashley [3 ]
Chan, Charles M. L. [1 ,2 ]
Chan, K. C. Allen [4 ]
Wong, S. C. Cesar [5 ]
Lo, Y. M. Dennis [4 ]
Chan, Anthony T. C. [1 ,2 ]
机构
[1] Chinese Univ Hong Kong, Hong Kong Canc Inst, Sir YK Pao Ctr Canc, State Key Lab Oncol South China,Dept Clin Oncol, Sha Tin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Sha Tin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Diagnost & Intervent Radiol, Sha Tin, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Chem Pathol, Sha Tin, Hong Kong, Peoples R China
[5] Polytech Univ, Dept Hlth Technol & Informat, Fac Hlth & Social Sci, Hong Kong, Hong Kong, Peoples R China
关键词
RANDOMIZED CONTROLLED-TRIAL; CONCURRENT CHEMORADIOTHERAPY; COLORECTAL-CANCER; RADIOTHERAPY; THERAPY; PET/CT; CHEMORADIATION; MULTICENTER; TOMOGRAPHY; MANAGEMENT;
D O I
10.1038/s41416-018-0026-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Plasma Epstein-Barr virus (pEBV) DNA and fluorodeoxyglucose positron emission (PET) reflect tumour burden in advanced NPC. This study hypothesised that a dual endpoint based on assessing pEBV DNA clearance and PET response could predict early drug response. METHODS: Eligible patients underwent a computed tomography (CT) scan and dual PET-CT at baseline, a PET-CT at 4 weeks, and then a CT scan at 10 weeks after starting palliative or induction chemotherapy. Plasma EBV DNA clearance was determined. RESULTS: Fifty-eight out of 70 enrolled patients completed all imaging and 50/58 had falling pEBV DNA level, which allowed calculation of the clearance. At a median follow-up of 29.1 months, the dual endpoint (pEBV DNA clearance <= 10 days and > 50% drop in sum of SUVmax of target lesions) was an independent indicator of overall survival (hazard ratio (HR) = 0.135, 95% CI = 0.039 to 0.466, p = 0.0015) and progression-free survival (HR = 0.136, 95% CI = 0.048 to 0.385, p = 0002). This dual endpoint could predict subsequent response by Response Evaluation Criteria In Solid Tumours (RECIST) criteria at 10 weeks after chemotherapy. CONCLUSIONS: Early PET-CT response and pEBV DNA clearance could predict survival and subsequent response. This dual endpoint is an innovative tool for assessing early drug response.
引用
收藏
页码:1051 / 1055
页数:5
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