Reduced‐volume radiotherapy versus conventional‐volume radiotherapy after induction chemotherapy in nasopharyngeal carcinoma: An open‐label, noninferiority, multicenter, randomized phase 3 trial.

Tang, Ling‐Long; Chen, Lin; Xu, Gui‐Qiong; Zhang, Ning; Huang, Cheng‐Long; Li, Wen‐Fei; Mao, Yan‐Ping; Zhou, Guan‐Qun; Lei, Feng; Chen, Lu‐Si; Huang, Shao Hui; Chen, Lei; Chen, Yu‐Pei; Zhang, Yuan; Liu, Xu; Xu, Cheng; Zhao, Yin; Li, Ji‐Bin; Liu, Na; Xie, Fang‐Yun

Background: Nearly 90% locoregionally advanced nasopharyngeal carcinoma (LANPC) responds to induction chemotherapy (IC) with significant tumor volume shrinkage. Radiotherapy always follows IC, and reduced volume has been proposed. However, the efficacy and safety of reduced‐volume radiotherapy is uncertain. Methods: In this multi‐center, noninferiority, randomized, controlled trial, patients with LANPC who completed IC were randomly assigned (1:1) to receive reduced‐volume radiotherapy based on post‐IC tumor volume (Post‐IC group) or conventional volume radiotherapy based on pre‐IC tumor volume (Pre‐IC group). The primary endpoint was locoregional relapse‐free survival, with a noninferiority margin of 8%. Secondary endpoints comprised adverse events, and quality of life (QoL). Results: Between August 7, 2020, and May 27, 2022, 445 patients were randomly assigned to Post‐IC (n = 225) or Pre‐IC (n = 220) groups. The average volume receiving radical dose was 66.6 cm3 in Post‐IC group versus 80.9 cm3. After a median follow‐up of 40.4 months, the 3‐year locoregional relapse‐free survival was 91.5% in the Post‐IC group versus 91.2%, with a difference of 0.3% (95% confidence interval −4.9% to 5.5%). The incidence of grade 3‐4 radiation‐related toxicity was lower in the Post‐IC group including: acute mucositis (19.8% vs 34.1%), late otitis media (9.5% vs 20.9%) and late dry month (3.6% vs 9.5%). The Post‐IC group had better QoL for global health status, physical functioning, emotional functioning, dry mouth and sticky saliva. Conclusions: In this trial, reduced‐volume radiotherapy was noninferior to conventional volume radiotherapy in locoregional relapse‐free survival, and was associated with lower toxicities and improved QoL. (ClinicalTrials.gov identifier NCT04384627).

CHINA; MUCOSITIS; OTITIS media; DOSE-response relationship (Radiation); RADIOTHERAPY; RESEARCH funding; ACADEMIC medical centers; STATISTICAL sampling; CLINICAL trials; RADIATION injuries; RANDOMIZED controlled trials; CANCER patients; FUNCTIONAL status; RESEARCH; QUALITY of life; NASOPHARYNX cancer; RADIATION doses; COMPARATIVE studies; PROGRESSION-free survival; INDUCTION chemotherapy

CA: A Cancer Journal for Clinicians, 2025, Vol 75, Issue 3, p203

0007-9235

Academic Journal

10.3322/caac.21881