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Study identifier: NCT07154069 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Adaptive Immunotherapy for Nasopharyngeal Carcinoma

Condition: Nasopharyngeal Cancinoma (NPC)  ·  Sponsor: Sun Yat-sen University

PhasePhase 3
Planned participants802
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

1. To assess whether radiotherapy alone is non-inferior to concurrent chemoradiotherapy with respect to event-free survival and superior in reducing treatment-related nausea in low-risk locoregionally advanced nasopharyngeal carcinoma patients who achieve complete or partial response and undetectable serum EBV-DNA following induction chemoimmunotherapy. 2. To evaluate whether adjuvant capecitabine and immunotherapy after concurrent chemoradiotherapy improves event-free survival compared to adjuvant immunotherapy in high-risk locoregionally advanced nasopharyngeal carcinoma patients with stable disease or detectable serum EBV-DNA after induction chemoimmunotherapy.

This description comes directly from the study's public registry record.

Talk to the study team

Ling-Long Tang  ·  02087343840  ·  tangll@sysucc.org.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Sun Yat-sen University Cancer CenterGuangzhou, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07154069