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利用 F-FDG PET/CT 参数和 Epstein-Barr 病毒 DNA 载量对初治鼻咽癌患者进行早期疗效评估预测价值。

Value of early evaluation of treatment response using F-FDG PET/CT parameters and the Epstein-Barr virus DNA load for prediction of outcome in patients with primary nasopharyngeal carcinoma.

机构信息

Department of Nuclear Medicine, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan.

Department of Otorhinolaryngology, Linkou Chang Gung Memorial Hospital and Chang Gung University, Taoyuan, Taiwan.

出版信息

Eur J Nucl Med Mol Imaging. 2019 Mar;46(3):650-660. doi: 10.1007/s00259-018-4172-3. Epub 2018 Sep 27.

Abstract

PURPOSE

To determine the value of early evaluation of response to concurrent chemoradiotherapy (CCRT) using F-FDG PET-derived parameters and the Epstein-Barr virus (EBV) DNA titre in outcome prediction in patients with primary nasopharyngeal carcinoma (NPC).

METHODS

Sixty patients with primary NPC were prospectively enrolled. All patients underwent F-FDG PET/CT before and during CCRT. The plasma EBV DNA titre was measured along with the PET/CT-derived parameters. Changes in EBV DNA titre and PET/CT-derived parameters during CCRT were analysed in relation to response to treatment, recurrence-free survival (RFS) and overall survival (OS).

RESULTS

A total lesion glycolysis (TLG) reduction ratio of ≤0.6 and a detectable EBV DNA titre during CCRT were predictors of an unfavourable response to treatment, RFS and OS. In multivariate analysis, a TLG reduction ratio of ≤0.6 predicted incomplete remission (p = 0.002) and decreased RFS (p = 0.003). The proportion of patients with a TLG reduction ratio of >0.6 who achieved a complete response was more than twice that of patients with a TLG reduction ratio of ≤0.6. A detectable EBV DNA titre, a TLG reduction ratio of ≤0.6 and older age were independently associated with a poorer OS (p = 0.037, 0.009 and 0.016, respectively). A scoring system was developed based on these independent predictors of OS. Patients with a score of 1 and 2/3 had poorer survival outcomes than those with a score of 0 (hazard ratio 4.756, p = 0.074, and hazard ratio 18.973, p = 0.001, respectively). This scoring system appeared to be superior to the traditional TNM staging system (p < 0.001 versus p = 0.175).

CONCLUSION

Early evaluation of response to CCRT using F-FDG PET-derived parameters and the EBV DNA titre can predict outcome in patients with primary NPC. A combination of interim PET parameters and the EBV DNA titre enables better stratification of patients into subgroups with different survival rates.

摘要

目的

确定使用 F-FDG PET 衍生参数和 Epstein-Barr 病毒(EBV)DNA 载量评估同期放化疗(CCRT)早期反应在预测原发性鼻咽癌(NPC)患者结局中的价值。

方法

前瞻性纳入 60 例原发性 NPC 患者。所有患者在 CCRT 前和期间均进行 F-FDG PET/CT 检查。同时检测血浆 EBV DNA 载量和 PET/CT 衍生参数。分析 CCRT 期间 EBV DNA 载量和 PET/CT 衍生参数的变化与治疗反应、无复发生存(RFS)和总生存(OS)的关系。

结果

CCRT 期间总病灶糖酵解(TLG)降低率≤0.6 和可检测到 EBV DNA 载量是治疗反应不良、RFS 和 OS 的预测因素。多变量分析显示,TLG 降低率≤0.6 预测不完全缓解(p=0.002)和 RFS 降低(p=0.003)。TLG 降低率>0.6 的患者完全缓解的比例是 TLG 降低率≤0.6 的患者的两倍多。可检测到的 EBV DNA 载量、TLG 降低率≤0.6 和年龄较大与较差的 OS 独立相关(p=0.037、0.009 和 0.016)。根据 OS 的这些独立预测因素制定了评分系统。评分 1 和 2/3 的患者的生存结果比评分 0 的患者差(风险比 4.756,p=0.074,和风险比 18.973,p=0.001)。该评分系统似乎优于传统的 TNM 分期系统(p<0.001 与 p=0.175)。

结论

使用 F-FDG PET 衍生参数和 EBV DNA 载量早期评估 CCRT 反应可预测原发性 NPC 患者的结局。中期 PET 参数和 EBV DNA 载量的组合可更好地将患者分层为具有不同生存率的亚组。

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