Alfieri Salvatore, Romanò Rebecca, Marceglia Sara, Sciortino Carolina, Ferrari Bravo Walter, Zucchini Monica, Piscitelli Maria Luigia, Nuzzolese Imperia, Cavalieri Stefano, Bergamini Cristiana, Colombo Elena, Ottini Arianna, De Cecco Loris, Lenoci Deborah, Iacovelli Nicola Alessandro, Guzzo Marco, Orlandi Ester, Locati Laura Deborah, Bossi Paolo, Licitra Lisa, Taverna Francesca
Department of Head and Neck Medical Oncology, Fondazione IRCCS - Istituto Nazionale dei Tumori, Milano, Italy.
Department of Health Sciences, University of Milan, Milano, Italy.
Eur J Cancer. 2025 Aug 26;226:115625. doi: 10.1016/j.ejca.2025.115625. Epub 2025 Jul 9.
Plasma Epstein Barr Virus (EBV)-DNA is an established biomarker for endemic EBV-related nasopharyngeal carcinoma (NPC). Its relevance in non-endemic regions is less understood. This study longitudinally assessed plasma EBV-DNA (LEA study) throughout the curative management of non-endemic EBV-related NPC to evaluate its prognostic value.
Between 2012 and 2023, patients with non-endemic, non-metastatic, histologically confirmed EBER+ NPC treated at a tertiary center were retrospectively analyzed. Plasma EBV-DNA levels were measured at pre-treatment (T1), early (T2a, ≤6 weeks) and late (T2b, ≤14 weeks) post-treatment, during follow-up (T3), and after induction chemotherapy (T4), when applicable. EBV-DNA was analyzed for its association with recurrence-free survival (RFS).
At a median follow-up of 60 months (range: 9-134), 167 patients were included. Median age was 50 years (range: 22-75), with 72 % male; 84 % had stage III-IV disease (TNM VIII Edition). Pre-treatment EBV-DNA was detected in 96 % of patients, with no predictive cut-off (median RFS: 43 vs. 62 months for detectable vs. undetectable EBV-DNA). Post-treatment undetectable EBV-DNA correlated with better RFS, also with no cut-off. Follow-up EBV-DNA anticipated recurrence in 71 % of cases by a median of 38 days (range: 11-365). Persistently negative follow-up EBV-DNA was observed in 91 % of non-recurrent patients; isolated positive spikes lacked prognostic significance. Post-induction chemotherapy EBV-DNA demonstrated a 92 % negative predictive value for recurrence.
Plasma EBV-DNA is a valuable prognostic biomarker for non-endemic NPC. Pre- and post-treatment undetectable EBV-DNA holds a positive prognostic value. Post-induction EBV-DNA is the most informative timepoint. Longitudinal EBV-DNA monitoring is warranted in clinical practice.
血浆爱泼斯坦-巴尔病毒(EBV)-DNA是地方性EBV相关鼻咽癌(NPC)的一种既定生物标志物。其在非地方性地区的相关性尚鲜为人知。本研究在非地方性EBV相关NPC的根治性治疗过程中纵向评估血浆EBV-DNA(LEA研究),以评估其预后价值。
回顾性分析2012年至2023年期间在一家三级中心接受治疗的非地方性、非转移性、组织学确诊为EBER+ NPC患者。在治疗前(T1)、治疗后早期(T2a,≤6周)和晚期(T2b,≤14周)、随访期间(T3)以及适用时在诱导化疗后(T4)测量血浆EBV-DNA水平。分析EBV-DNA与无复发生存期(RFS)的相关性。
中位随访60个月(范围:9 - 134个月),纳入167例患者。中位年龄为50岁(范围:22 - 75岁),男性占72%;84%为III - IV期疾病(TNM第八版)。96%的患者在治疗前检测到EBV-DNA,无预测临界值(可检测与不可检测EBV-DNA的中位RFS分别为43个月和62个月)。治疗后EBV-DNA不可检测与更好的RFS相关联,也无临界值。随访EBV-DNA在71%的病例中预测复发,中位提前38天(范围:11 - 365天)。91%的未复发患者随访EBV-DNA持续为阴性;孤立的阳性峰值缺乏预后意义。诱导化疗后EBV-DNA对复发的阴性预测值为92%。
血浆EBV-DNA是用于非地方性NPC的有价值的预后生物标志物。治疗前和治疗后EBV-DNA不可检测具有良好的预后价值。诱导化疗后EBV-DNA是最具信息价值的时间点。临床实践中进行纵向EBV-DNA监测是必要的。