Dose-volume relationship for laryngeal substructures and aspiration in patients with locally advanced head-and-neck cancer.


Journal

Radiation oncology (London, England)
ISSN: 1748-717X
Titre abrégé: Radiat Oncol
Pays: England
ID NLM: 101265111

Informations de publication

Date de publication:
18 Mar 2019
Historique:
received: 30 10 2018
accepted: 01 03 2019
entrez: 20 3 2019
pubmed: 20 3 2019
medline: 29 5 2019
Statut: epublish

Résumé

Literature has shown a significant relationship between radiation dose to the larynx and swallowing disorders. We prospectively studied the dose-volume relationship for larynx substructures and aspiration. Forty nine patients with stage III/IV head-and-neck (H&N) squamous cell carcinoma were prospectively enrolled in this IRB-approved, federally funded study. All patients received IMRT-based chemoradiation therapy (CRT) and were scheduled for videofluorography (VFG) prior to CRT and at 3, 6, 9, 12, and 24 months post-CRT. Twelve laryngeal substructures were contoured in each patient: thyroid cartilage, cricoid cartilage, total epiglottis, suprahyoid epiglottis, infrahyoid epiglottis, total larynx, supraglottic larynx, subglottic larynx, glottic larynx, arytenoids, aryepiglottic (AE) folds, and glossoepiglottic fold. After exclusions, 29 patients were included in the final analysis. Incidence of aspiration at 1 year following CRT was correlated with dose-volume data to laryngeal substructures using logistic regression. The median age was 54 years with 79% being non-smokers. Tumor sites included oropharynx (22), unknown primary (6), and hypopharynx (1). One year following CRT, 10/29 (34%) showed aspiration on VFG. Dose to the AE folds showed the highest correlation with aspiration at 12 months and was significant on multivariate analysis (p = 0.025). A mean dose cutpoint of 6500 cGy or higher to the AE folds was associated with an increased risk of aspiration at 1 year [positive likelihood ratio (+LR) 2.81, positive predictive value (PPV) 60%, negative predictive value (NPV) 92.9%, relative risk (RR) 8.4]. In this analysis, mean dose to the AE folds was associated with an increased risk of aspiration at 1 year. However, these are hypothesis-generating data that require further research and validation in a larger patient subset.

Sections du résumé

BACKGROUND BACKGROUND
Literature has shown a significant relationship between radiation dose to the larynx and swallowing disorders. We prospectively studied the dose-volume relationship for larynx substructures and aspiration.
METHODS METHODS
Forty nine patients with stage III/IV head-and-neck (H&N) squamous cell carcinoma were prospectively enrolled in this IRB-approved, federally funded study. All patients received IMRT-based chemoradiation therapy (CRT) and were scheduled for videofluorography (VFG) prior to CRT and at 3, 6, 9, 12, and 24 months post-CRT. Twelve laryngeal substructures were contoured in each patient: thyroid cartilage, cricoid cartilage, total epiglottis, suprahyoid epiglottis, infrahyoid epiglottis, total larynx, supraglottic larynx, subglottic larynx, glottic larynx, arytenoids, aryepiglottic (AE) folds, and glossoepiglottic fold. After exclusions, 29 patients were included in the final analysis. Incidence of aspiration at 1 year following CRT was correlated with dose-volume data to laryngeal substructures using logistic regression.
RESULTS RESULTS
The median age was 54 years with 79% being non-smokers. Tumor sites included oropharynx (22), unknown primary (6), and hypopharynx (1). One year following CRT, 10/29 (34%) showed aspiration on VFG. Dose to the AE folds showed the highest correlation with aspiration at 12 months and was significant on multivariate analysis (p = 0.025). A mean dose cutpoint of 6500 cGy or higher to the AE folds was associated with an increased risk of aspiration at 1 year [positive likelihood ratio (+LR) 2.81, positive predictive value (PPV) 60%, negative predictive value (NPV) 92.9%, relative risk (RR) 8.4].
CONCLUSIONS CONCLUSIONS
In this analysis, mean dose to the AE folds was associated with an increased risk of aspiration at 1 year. However, these are hypothesis-generating data that require further research and validation in a larger patient subset.

Identifiants

pubmed: 30885235
doi: 10.1186/s13014-019-1247-7
pii: 10.1186/s13014-019-1247-7
pmc: PMC6423881
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

49

Subventions

Organisme : NIDCD NIH HHS
ID : R01 DC007659
Pays : United States
Organisme : National Institutes of Health
ID : R01 DC007659

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Auteurs

Katarina G Petras (KG)

Department of Radiation Oncology, Northwestern University, Chicago, IL, USA.
Department of Radiation Oncology, NMH, 251 E. Huron Street, LC-178, Chicago, IL, 60611, USA.

Alfred W Rademaker (AW)

Biostatistics Department, Northwestern University, Chicago, IL, USA.
Department of Biostatistics & Preventative Medicine, 680 N. Lakeshore Drive, Suite 1400, Chicago, IL, 60611, USA.

Tamer Refaat (T)

Department of Clinical Oncology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Department of Radiation Oncology, Loyola University Medical Center, Maguire Center - Room 2944, 2160 S. 1st Avenue, Maywood, IL, 60153, USA.

Mehee Choi (M)

Rush Copley Medical Center, 2000 Ogden Avenue, Aurora, IL, 60504, USA.

Tarita O Thomas (TO)

Department of Radiation Oncology, Loyola University Medical Center, Maguire Center - Room 2944, 2160 S. 1st Avenue, Maywood, IL, 60153, USA.

Barbara R Pauloski (BR)

Department of Communication Sciences and Disorders, College of Health Sciences, University of Wisconsin-Milwaukee, Enderis Hall, Room 845, 2400 E. Hartford, Avenue, Milwaukee, WI, 53211, USA.

Bharat B Mittal (BB)

Department of Radiation Oncology, Northwestern University, Chicago, IL, USA. bharat.mittal@nm.org.
Department of Radiation Oncology, NMH, 251 E. Huron Street, LC-178, Chicago, IL, 60611, USA. bharat.mittal@nm.org.

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Classifications MeSH