TY - JOUR
T1 - Beyond mean pharyngeal constrictor dose for beam path toxicity in non-target swallowing muscles
T2 - Dose-volume correlates of chronic radiation-associated dysphagia (RAD) after oropharyngeal intensity modulated radiotherapy
AU - MD Anderson Head and Neck Cancer Symptom Working Group
AU - Dale, Timothy
AU - Hutcheson, Katherine
AU - Mohamed, Abdallah S.R.
AU - Lewin, Jan S.
AU - Gunn, G. Brandon
AU - Rao, Arvind U.K.
AU - Kalpathy-Cramer, Jayashree
AU - Frank, Steven J.
AU - Garden, Adam S.
AU - Messer, Jay A.
AU - Warren, Benjamin
AU - Lai, Stephen Y.
AU - Beadle, Beth M.
AU - Morrison, William H.
AU - Phan, Jack
AU - Skinner, Heath
AU - Gross, Neil
AU - Ferrarotto, Renata
AU - Weber, Randal S.
AU - Rosenthal, David I.
AU - Fuller, Clifton D.
N1 - Funding Information:
Dr. Fuller received/receives grant and/or salary support from: National Science Foundation, Division of Mathematical Sciences Quantitative Approaches to Biomedical Big Data (QuBBD) Program (NSF 1557559); the National Institutes of Health/National Cancer Institute’s Paul Calabresi Clinical Oncology Award Program (K12 CA088084-06) and Clinician Scientist Loan Repayment Program (L30 CA136381-02); the SWOG/Hope Foundation Dr. Charles A. Coltman, Jr., Fellowship in Clinical Trials; a General Electric Healthcare/MD Anderson Center for Advanced Biomedical Imaging In-Kind Award; an Elekta AB/MD Anderson Department of Radiation Oncology Seed Grant; the Center for Radiation Oncology Research at MD Anderson Cancer Center; and the MD Anderson Institutional Research Grant Program. Drs. Lai, Mohamed, and Fuller are supported by a grant award from the National Institutes of Health/National Institute for Dental and Craniofacial Research (1R56DE025248-01). Dr. Hutcheson receives grant support from the MD Anderson Institutional Research Grant Program and the National Cancer Institute (R03 CA188162). This work was supported in part infrastructure support by National Institutes of Health Cancer Center Support (Core) Grant CA016672 to The University of Texas MD Anderson Cancer Center. These listed funders/supporters played no role in the study design, collection, analysis, interpretation of data, manuscript writing, or decision to submit the report for publication.
Publisher Copyright:
© 2016 Elsevier Ireland Ltd.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Purpose/objective(s) We sought to identify swallowing muscle dose-response thresholds associated with chronic radiation-associated dysphagia (RAD) after IMRT for oropharyngeal cancer. Materials/methods T1-4 N0-3 M0 oropharyngeal cancer patients who received definitive IMRT and systemic therapy were examined. Chronic RAD was coded as any of the following ≥12 months post-IMRT: videofluoroscopy/endoscopy detected aspiration or stricture, gastrostomy tube and/or aspiration pneumonia. DICOM-RT plan data were autosegmented using a custom region-of-interest (ROI) library and included inferior, middle and superior constrictors (IPC, MPC, and SPC), medial and lateral pterygoids (MPM, LPM), anterior and posterior digastrics (ADM, PDM), intrinsic tongue muscles (ITM), mylo/geniohyoid complex (MHM), genioglossus (GGM), masseter (MM), buccinator (BM), palatoglossus (PGM), and cricopharyngeus (CPM), with ROI dose-volume histograms (DVHs) calculated. Recursive partitioning analysis (RPA) was used to identify dose-volume effects associated with chronic-RAD, for use in a multivariate (MV) model. Results Of 300 patients, 34 (11%) had chronic-RAD. RPA showed DVH-derived MHM V69 (i.e. the volume receiving ≥ 69 Gy), GGM V35, ADM V60, MPC V49, and SPC V70 were associated with chronic-RAD. A model including age in addition to MHM V69 as continuous variables was optimal among tested MV models (AUC 0.835). Conclusion In addition to SPCs, dose to MHM should be monitored and constrained, especially in older patients (>62-years), when feasible.
AB - Purpose/objective(s) We sought to identify swallowing muscle dose-response thresholds associated with chronic radiation-associated dysphagia (RAD) after IMRT for oropharyngeal cancer. Materials/methods T1-4 N0-3 M0 oropharyngeal cancer patients who received definitive IMRT and systemic therapy were examined. Chronic RAD was coded as any of the following ≥12 months post-IMRT: videofluoroscopy/endoscopy detected aspiration or stricture, gastrostomy tube and/or aspiration pneumonia. DICOM-RT plan data were autosegmented using a custom region-of-interest (ROI) library and included inferior, middle and superior constrictors (IPC, MPC, and SPC), medial and lateral pterygoids (MPM, LPM), anterior and posterior digastrics (ADM, PDM), intrinsic tongue muscles (ITM), mylo/geniohyoid complex (MHM), genioglossus (GGM), masseter (MM), buccinator (BM), palatoglossus (PGM), and cricopharyngeus (CPM), with ROI dose-volume histograms (DVHs) calculated. Recursive partitioning analysis (RPA) was used to identify dose-volume effects associated with chronic-RAD, for use in a multivariate (MV) model. Results Of 300 patients, 34 (11%) had chronic-RAD. RPA showed DVH-derived MHM V69 (i.e. the volume receiving ≥ 69 Gy), GGM V35, ADM V60, MPC V49, and SPC V70 were associated with chronic-RAD. A model including age in addition to MHM V69 as continuous variables was optimal among tested MV models (AUC 0.835). Conclusion In addition to SPCs, dose to MHM should be monitored and constrained, especially in older patients (>62-years), when feasible.
KW - Dose-volume
KW - Dysphagia
KW - Geniohyoid
KW - Intensity-modulated radiation therapy
KW - Mylohyoid
KW - Oropharyngeal cancer
UR - http://www.scopus.com/inward/record.url?scp=84960214755&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84960214755&partnerID=8YFLogxK
U2 - 10.1016/j.radonc.2016.01.019
DO - 10.1016/j.radonc.2016.01.019
M3 - Article
C2 - 26897515
AN - SCOPUS:84960214755
SN - 0167-8140
VL - 118
SP - 304
EP - 314
JO - Radiotherapy and Oncology
JF - Radiotherapy and Oncology
IS - 2
ER -