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Four-Week Hypofractionated Radiotherapy for Early Glottic Cancer: A Prospective Study of Toxicity and Tolerance With
Georgios Moschos1, Alexia Theodoridou1, Areti Gkantaifi1
1Department of Radiation Oncology, American Hellenic Educational Progressive Association (AHEPA) University Hospital, Thessaloniki, GRC.
Cureus
|December 24, 2025
Summary
This study shows that hypofractionated radiotherapy using volumetric modulated arc therapy (VMAT) is a safe and effective treatment for early glottic carcinoma, achieving high local control rates with manageable toxicity.
Area of Science:
- Radiation Oncology
- Head and Neck Cancer
- Glottic Carcinoma Treatment
Background:
- Hypofractionated radiotherapy is increasingly used for early glottic cancer to improve tumor control and reduce treatment time.
- Limited data exists for hypofractionated regimens exceeding 2.5 Gy per fraction, especially for T2 glottic tumors.
Purpose of the Study:
- To evaluate the safety and efficacy of a hypofractionated radiotherapy regimen (55 Gy in 20 fractions) using VMAT for early glottic carcinoma.
- To assess toxicity and local control rates in patients with T1-T2N0M0 glottic cancer.
Main Methods:
- Prospective interventional study involving 23 patients with T1-T2N0M0 glottic carcinoma.
- Treatment delivered via volumetric modulated arc therapy (VMAT) at 55 Gy in 20 fractions (2.75 Gy/fraction) with daily image guidance.
- Primary endpoint: toxicity; Secondary endpoint: local control.
Main Results:
- A complete response was achieved in 95.7% of patients; one patient required salvage surgery.
- One-year local control rates were 91.7% for T1 and 85.7% for T2 disease, with overall 91.3%.
- Predominantly Grade 1-2 acute toxicities observed; Grade 3 events included hoarseness and dysphagia. Late toxicities were generally mild.
Conclusions:
- Hypofractionated VMAT (55 Gy/20 fractions) is a feasible and safe treatment for early glottic carcinoma.
- The regimen provides excellent tumor control for T1 disease and acceptable outcomes for T2 disease with low toxicity.
- Further research with longer follow-up and larger cohorts is needed to confirm long-term local control, particularly for T2 tumors.

