Association of Risk Factors With Patient-Reported Voice and Speech Symptoms Among Long-term Survivors of Oropharyngeal Cancer.


Journal

JAMA otolaryngology-- head & neck surgery
ISSN: 2168-619X
Titre abrégé: JAMA Otolaryngol Head Neck Surg
Pays: United States
ID NLM: 101589542

Informations de publication

Date de publication:
01 07 2021
Historique:
pubmed: 7 5 2021
medline: 21 10 2021
entrez: 6 5 2021
Statut: ppublish

Résumé

Voice and speech production are critical physiological functions that affect quality of life and may deteriorate substantially after oropharyngeal cancer (OPC) treatment. There is limited knowledge about risk factors associated with voice and speech outcomes among survivors of OPC. To identify the risk factors of voice and speech symptoms among long-term survivors of OPC. This retrospective cohort study with cross-sectional survivorship survey administration includes cancer-free survivors of OPC who were treated curatively between January 2000 and December 2013 at MD Anderson Cancer Center (Houston, Texas) who participated in a survey from September 2015 to July 2016. Of 906 survivors of OPC with a median survival duration at time of survey of 6 years (range, 1-16 years), patient-rated voice and speech outcomes for 881 were available and analyzed. The data were analyzed from June 30, 2020, to February 28, 2021. The primary outcome variable was patient-reported voice and speech scores that were measured using the MD Anderson Symptom Inventory-Head and Neck Cancer Module. Voice and speech scores of 0 to 4 were categorized as none to mild symptoms, and scores of 5 to 10 were categorized as moderate to severe symptoms. Risk factors for moderate to severe voice and speech symptoms were identified by multivariable logistic regression. Among 881 survivors of OPC (median [range] age, 56 [32-84] years; 140 women [15.5%]; 837 White [92.4%], 17 Black [1.9%], and 35 Hispanic individuals [3.8%]), 113 (12.8%) reported moderate to severe voice and speech scores. Increasing survival time (odds ratio [OR], 1.17; 95% CI, 1.06-1.30) and increasing total radiation dose (OR, 1.16; 95% CI, 1.00-1.34), Black race (OR, 3.90; 95% CI, 1.02-14.89), Hispanic ethnicity (OR, 3.74; 95% CI, 1.50-9.35), current cigarette smoking at the time of survey (OR, 3.98; 95% CI, 1.56-10.18), treatment with induction and concurrent chemotherapy (OR, 1.94; 95% CI, 1.06-3.57), and late (OR, 7.11; 95% CI, 3.08-16.41) and baseline lower cranial neuropathy (OR, 8.70; 95% CI, 3.01-25.13) were risk factors associated with moderate to severe voice and speech symptoms. Intensity-modulated radiotherapy split-field regimen (OR, 0.31; 95% CI, 0.12-0.80; P = .01) was associated with lower likelihood of moderate to severe voice and speech symptoms. This large OPC survivorship cohort study identified many treatment-related factors, including increasing total radiotherapy dose, multimodality induction and concurrent chemotherapy regimens, and continued smoking, as well as clinical and demographic factors, as risk factors that were associated with moderate to severe voice and speech symptoms. The key findings in this study were the protective associations of split-field radiation and that longer-term survivors, and those who continued to smoke, had worse voice and speech symptoms. These findings may inform research and effective targeted clinical voice and speech preservation interventions and smoking cessation interventions to maximize voice and speech function and address quality of life among patients with OPC.

Identifiants

pubmed: 33956062
pii: 2779628
doi: 10.1001/jamaoto.2021.0698
pmc: PMC8103354
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

615-623

Subventions

Organisme : NCI NIH HHS
ID : R01 CA258827
Pays : United States

Auteurs

Puja Aggarwal (P)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston.

Katherine A Hutcheson (KA)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Adam S Garden (AS)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Frank E Mott (FE)

Department of Thoracic Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Ryan P Goepfert (RP)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Amber Duvall (A)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Clifton D Fuller (CD)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Stephen Y Lai (SY)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

G Brandon Gunn (GB)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Erich M Sturgis (EM)

Department of Otolaryngology-Head and Neck Surgery, Baylor College of Medicine, Houston, Texas.

Ehab Y Hanna (EY)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Sanjay Shete (S)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston.
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston.
Division of Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston.

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