Journal article
SBRT for early-stage glottic larynx cancer-Initial clinical outcomes from a phase I clinical trial
PloS one, Vol.12(3), e0172055
2017
DOI: 10.1371/journal.pone.0172055
PMCID: PMC5333979
PMID: 28253270
Abstract
To confirm safety and feasibility of hypofractionated SBRT for early-stage glottic laryngeal cancer. Twenty consecutive patients with cTis-T2N0M0 carcinoma of glottic larynx were enrolled. Patients entered dose-fractionation cohorts of incrementally shorter bio-equivalent schedules starting with 50 Gy in 15 fractions (fx), followed by 45 Gy/10 fx and, finally, 42.5 Gy/5 fx. Maximum combined CTV-PTV expansion was limited to 5 mm. Patients were treated on a Model G5 Cyberknife (Accuray, Sunnyvale, CA). Median follow-up is 13.4 months (range: 5.6-24.6 months), with 12 patients followed for at least one year. Maximum acute toxicity consisted of grade 2 hoarseness and dysphagia. Maximum chronic toxicity was seen in one patient treated with 45 Gy/10 fx who continued to smoke >1 pack/day and ultimately required protective tracheostomy. At 1-year follow-up, estimated local disease free survival for the full cohort was 82%. Overall survival is 100% at last follow-up. We were able to reduce equipotent total fractions of SBRT from 15 to 5 without exceeding protocol-defined acute/subacute toxicity limits. With limited follow-up, disease control appears comparable to standard treatment. We continue to enroll to the 42.5 Gy/5 fx cohort and follow patients for late toxicity. ClinicalTrials.gov NCT01984502.
Details
- Title: Subtitle
- SBRT for early-stage glottic larynx cancer-Initial clinical outcomes from a phase I clinical trial
- Creators
- David L Schwartz - Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of AmericaAlan Sosa - Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of AmericaStephen G Chun - Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of AmericaChiuxiong Ding - Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of AmericaXian-Jin Xie - Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of AmericaLucien A Nedzi - Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of AmericaRobert D Timmerman - Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of AmericaBaran D Sumer - Department of Otolaryngology, Head and Neck Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America
- Resource Type
- Journal article
- Publication Details
- PloS one, Vol.12(3), e0172055
- DOI
- 10.1371/journal.pone.0172055
- PMID
- 28253270
- PMCID
- PMC5333979
- NLM abbreviation
- PLoS One
- ISSN
- 1932-6203
- eISSN
- 1932-6203
- Publisher
- United States
- Grant note
- DOI: 10.13039/100004917, name: CPRIT, award: RP150386; DOI: 10.13039/100004917, name: CPRIT, award: RP150485
- Language
- English
- Date published
- 2017
- Academic Unit
- Preventive and Community Dentistry; Biostatistics; Dental Research
- Record Identifier
- 9983917675202771
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