State Key Laboratory of Oncology in South China, Sir Y K Pao Centre for Cancer, Department of Clinical Oncology, Hong Kong Cancer Institute and Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong SAR.
Department of Diagnostic and Interventional Radiology, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong SAR.
Br J Cancer. 2018 Apr;118(8):1051-1055. doi: 10.1038/s41416-018-0026-9. Epub 2018 Mar 20.
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.
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.
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.
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.
血浆 EBV 病毒(pEBV)DNA 和氟代脱氧葡萄糖正电子发射断层扫描(PET)反映了晚期 NPC 的肿瘤负荷。本研究假设,基于评估 pEBV DNA 清除率和 PET 反应的双重终点可以预测早期药物反应。
符合条件的患者在基线时进行计算机断层扫描(CT)和双 PET-CT 检查,在开始姑息性或诱导化疗后 4 周进行 PET-CT 检查,然后在 10 周时进行 CT 扫描。测定血浆 EBV DNA 清除率。
70 名入组患者中有 58 名完成了所有影像学检查,50/58 例患者的 pEBV DNA 水平下降,可计算清除率。中位随访 29.1 个月后,双重终点(pEBV DNA 清除率≤10 天且靶病灶 SUVmax 总和下降>50%)是总生存期(风险比(HR)=0.135,95%CI=0.039 至 0.466,p=0.0015)和无进展生存期(HR=0.136,95%CI=0.048 至 0.385,p=0.0002)的独立预测指标。这一双重终点可以预测化疗后 10 周时实体瘤反应评估标准(RECIST)的后续反应。
早期 PET-CT 反应和 pEBV DNA 清除率可预测生存和后续反应。这一双重终点是评估早期药物反应的创新工具。