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MRI-Guided Reduced-Volume RT for Early-Stage Glottic Cancer: A Prospective Phase 1 Trial with Quantification of Laryngeal Motion

Journal
International journal of radiation oncology, biology, physics (Q1)
Published
26 August 2026
Study design
Phase 1 (first-in-human) trial
Evidence level
Level 4, Very Low (CEBM 4)
Authors
Jonathan E Leeman, Alexander D Droznin, Christopher D Dwyer, Kee-Young Shin, Douglas F Roth, Sejal Chirmade, et al.
PMID
42648578
DOI
10.1016/j.ijrobp.2026.08.048

Why clinicians should know about it

  • Picked for Otorhinolaryngology (paper of the day, 31 August 2026): MRI‑guided reduced‑volume RT feasible for early glottic cancer

Abstract

PURPOSE: Five to 7 weeks of whole-larynx radiation (RT) is standard for treatment of early-stage glottic cancer. Previous studies evaluated CT-guided hypofractionated/SBRT treatment to a smaller volume. Magnetic resonance-guided radiotherapy (MRgRT) allows real-time motion tracking and gating by continuously imaging the larynx. We performed the first prospective study of MRgRT in patients with early-stage glottic cancer with quantification of laryngeal motion. METHODS AND MATERIALS: This phase 1 trial evaluated MRgRT in patients with stage I/II squamous cell glottic cancer undergoing definitive RT. The RT prescription was either 42.5 Gy/5 fractions (treatment volume < 10cc, not actively smoking) or 58.08 Gy/16 fractions (treatment volume > 10cc / smokers). Treatment was delivered using gated 0.35 T MRgRT with continuous tracking. Coprimary endpoints were feasibility and safety (grade 3+ toxicity rate). Patient-reported outcome measures (PROMs), voice quality, MRgRT treatment parameters, and local control were assessed. Intrafraction cine-MRI quantified laryngeal motion. RESULTS: MRgRT was feasible in all patients. Median time on study was 10.9 months. Treatment was well tolerated with no acute or late grade 3+ toxicities. There was no change in PROMs over the course of the study. Two patients who received 42.5 Gy experienced locoregional failure, one in-field only and one in-field and nodal. MR tracking resulted in 20/94 (21%) of treatment fractions requiring ≥ 1 shift necessitating intra-fraction re-imaging. In 19/94 (20%) of treatment fractions, the beam was off more than 20% of the treatment time due to stochastic beam interruption events (BIEs). During BIEs, larynx displacement exceeded 3 mm in 53% of cine-MRI frames. CONCLUSIONS: MRgRT targeting gross disease instead of the whole larynx is feasible and safe for patients with early-stage glottic cancer with minimal treatment-associated toxicity and no detriment in PROMs. MRI guidance provides real-time verification of larynx position. Data regarding real-time intrafraction motion has important implications for patients receiving standard laryngeal RT.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.