TY - JOUR
T1 - Risk factors of 131I-induced salivary gland damage in thyroid cancer patients
AU - Hollingsworth, Brynn
AU - Senter, Leigha
AU - Zhang, Xiaoli
AU - Brock, Guy N.
AU - Jarjour, Wael
AU - Nagy, Rebecca
AU - Brock, Pamela
AU - Coombes, Kevin R.
AU - Kloos, Richard T.
AU - Ringel, Matthew D.
AU - Sipos, Jennifer
AU - Lattimer, Ilene
AU - Carrau, Ricardo
AU - Jhiang, Sissy M.
N1 - Funding Information:
This work was supported in part by National Institutes of Health (NIH) Grant P50CA168505 (project leader, Sissy Jhiang; principal investigator, Matthew D. Ringel). B.H. is a recipient of NIH/National Institute of Dental and Craniofacial Research Grant T32 DE014320. Current affiliation of R.K.: Department of Medical Affairs, Veracyte, Inc., 6000 Shoreline Court, Suite 300, South San Francisco, CA 94080. Current affiliation of R.N.: Guardant Health, Inc., 505 Penobscot Drive, Redwood City, CA 94063.
Publisher Copyright:
Copyright © 2016 by the Endocrine Society.
PY - 2016/11
Y1 - 2016/11
N2 - Context: Sialadenitis and xerostomia are major adverse effects of 131I therapy in thyroid cancer patients. The risk factors for these adverse effects, other than administered activity of 131I, have not been investigated. Objective: The aim of this study is to identify risk factors for 131I-induced salivary gland damage among follicular cell-derived thyroid cancer patients. Design: We enrolled 216 thyroid cancer patients who visited The Ohio State University Wexner Medical Center between April 2013 and April 2014. Symptoms of xerostomia and sialadenitis were identified via questionnaire and medical record search. To validate the findings in a large cohort, we retrospectively searched for ICD-9/10 codes for sialadenitis, xerostomia, and autoimmune disease associated with Sjögren's syndrome (AID-SS) in our existing database (n=1507). Demographic and clinical information was extracted from medical records. Multivariate analyses were performed to identify independent predictors for salivary gland damage. Results: 131I treatment associated with higher incidence of xerostomia and sialadenitis. Patients with xerostomia had 46 mCi higher mean cumulative 131I activity and 21 mCi higher mean firstadministered 131I activity than patients without xerostomia. Increased age associated with higher incidence of xerostomia, and females had a higher incidence of sialadenitis. Patients who experienced sialadenitis before 131I therapy had higher sialadenitis incidence after 131I therapy. 131Itreated patients diagnosed with AID-SS, whether before or after 131I treatment, had a higher incidence of xerostomia and sialadenitis among 131I-treated patients. Conclusion: Risk factors for 131I-induced salivary gland damage include administered 131I activity, age, gender, history of sialadenitis before 131I treatment, and AID-SS diagnosis. (J Clin Endocrinol Metab 101: 4085-4093, 2016).
AB - Context: Sialadenitis and xerostomia are major adverse effects of 131I therapy in thyroid cancer patients. The risk factors for these adverse effects, other than administered activity of 131I, have not been investigated. Objective: The aim of this study is to identify risk factors for 131I-induced salivary gland damage among follicular cell-derived thyroid cancer patients. Design: We enrolled 216 thyroid cancer patients who visited The Ohio State University Wexner Medical Center between April 2013 and April 2014. Symptoms of xerostomia and sialadenitis were identified via questionnaire and medical record search. To validate the findings in a large cohort, we retrospectively searched for ICD-9/10 codes for sialadenitis, xerostomia, and autoimmune disease associated with Sjögren's syndrome (AID-SS) in our existing database (n=1507). Demographic and clinical information was extracted from medical records. Multivariate analyses were performed to identify independent predictors for salivary gland damage. Results: 131I treatment associated with higher incidence of xerostomia and sialadenitis. Patients with xerostomia had 46 mCi higher mean cumulative 131I activity and 21 mCi higher mean firstadministered 131I activity than patients without xerostomia. Increased age associated with higher incidence of xerostomia, and females had a higher incidence of sialadenitis. Patients who experienced sialadenitis before 131I therapy had higher sialadenitis incidence after 131I therapy. 131Itreated patients diagnosed with AID-SS, whether before or after 131I treatment, had a higher incidence of xerostomia and sialadenitis among 131I-treated patients. Conclusion: Risk factors for 131I-induced salivary gland damage include administered 131I activity, age, gender, history of sialadenitis before 131I treatment, and AID-SS diagnosis. (J Clin Endocrinol Metab 101: 4085-4093, 2016).
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U2 - 10.1210/jc.2016-1605
DO - 10.1210/jc.2016-1605
M3 - Article
C2 - 27533304
AN - SCOPUS:84994887817
SN - 0021-972X
VL - 101
SP - 4085
EP - 4093
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 11
ER -