A multicenter retrospective analysis of recurrent/metastatic nasopharyngeal cancer from non-endemic areas: Results in the pre-immunotherapy era
- PMID: 40912138
- DOI: 10.1016/j.ejca.2025.115749
A multicenter retrospective analysis of recurrent/metastatic nasopharyngeal cancer from non-endemic areas: Results in the pre-immunotherapy era
Abstract
Aim of the study: The aim of the study is to describe clinical features, treatment approach and outcomes of recurrent/metastatic (R/M) NPC in non-endemic areas MATERIALS AND METHODS: This observational, retrospective and multicenter study was conducted within 36 referral hospital in non-endemic areas including Europe, Jordan, Kuwait, Turkey and United States of America. All NPC patients diagnosed between 2004 and 2016 and with a minimum 12 months of follow-up were included. Data entry started in January 2018 and closed in December 2023.
Results: A total of 454 patients with R/M NPC were included in this analysis. The most frequent histology was non-keratinizing carcinoma (87 %); de novo metastatic patients had an EBV-related disease in 93 % of the cases. Among those with relapsed disease, locoregional recurrence was the most frequent site of recurrence, while bone was the principal site of metastatic dissemination (58 % of cases). Regarding treatment strategies, patients with loco-regional relapse received re-irradiation more frequently than salvage surgery (43 % vs 38 %). Overall, most of the patients with R/M disease received at least one line of systemic therapy. Median PFS was 13 months, while the median OS was 30 months (range 1-180) with a three year-OS rate of 47 %.
Conclusions: This study reports the largest available clinical data defining the outcome of non-endemic patients with R/M NPC. In the context of rare cancers, these data represent the benchmark to define new therapeutic strategies and confirms a similar behaviour of NPC between endemic and non-endemic NPC when correlated with EBV status.
Keywords: Nasopharyngeal cancer; Non-endemic areas; Pre-immunotherapy outcomes; Recurrence/metastasis.
Copyright © 2025 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: PB reported the following conflict of interests in the past 3 years: Participation to advisory board or conference honoraria for Merck, Sanofi-Regeneron, Merck Sharp & Dohme, Sun Pharma, Angelini, Nestlè, Elevar. LL reported the following conflict of interests in the past 3 years: Research funds donated directly to the institution for clinical trials I have participated in from: Adlai Nortye, Astrazeneca, BMS, Debiopharm International SA, Eisai, Eli Lilly and Company, Exelixis, Hoffmann-La Roche ltd, Isa Therapeutics, Kura Oncology, Merck-Serono, MSD, Merck Sharp&Dome Corp, Nektar Therapeutics, Novartis, Regeneron, Roche, Sanofi, Syneos, Sun Pharmaceutica. Occasional fees for participation as a speaker at conferences/congresses or as a scientific consultant for advisory boards from: Adlai Nortye, Astrazeneca, Bicara Therapeutics, DRG (part of Clarivate), Genmab US, GlaxoSmithKline, Bayer, Mirati Therapeutics, MSD, Merck-Serono, Merck Healthcare KGaA, Neutron Therapeutics Inc, Seagen International BmbH. All other authors reported no conflict of interest.
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