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The Global, Regional, and National Burden of Adult Lip, Oral, and Pharyngeal Cancer in 204 Countries and Territories: A Systematic Analysis for the Global Burden of Disease Study 2019

,; Cunha, Amanda Ramos da; Compton, Kelly; Xu, Rixing; Mishra, Rashmi; Drangsholt, Mark Thomas; Antunes, Jose Leopoldo Ferreira; Kerr, Alexander R; Acheson, Alistair R; Lu, Dan; Wallace, Lindsey E; Kocarnik, Jonathan M; Fu, Weijia; Dean, Frances E; Pennini, Alyssa; Henrikson, Hannah Jacqueline; Alam, Tahiya; Ababneh, Emad; Abd-Elsalam, Sherief; Abdoun, Meriem; Abidi, Hassan; Abubaker Ali, Hiwa; Abu-Gharbieh, Eman; Adane, Tigist Demssew; Addo, Isaac Yeboah; Ahmad, Aqeel; Ahmad, Sajjad; Ahmed Rashid, Tarik; Akonde, Maxwell; Al Hamad, Hanadi; Alahdab, Fares; Alimohamadi, Yousef; Alipour, Vahid; Al-Maweri, Sadeq Ali; Alsharif, Ubai; Ansari-Moghaddam, Alireza; Anwar, Sumadi Lukman; Anyasodor, Anayochukwu Edward; Arabloo, Jalal; Aravkin, Aleksandr Y; Aruleba, Raphael Taiwo; Asaad, Malke; Ashraf, Tahira; Athari, Seyyed Shamsadin; Attia, Sameh; Azadnajafabad, Sina; Azangou-Khyavy, Mohammadreza; Badar, Muhammad; Baghcheghi, Nayereh; Banach, Maciej; Bardhan, Mainak; Barqawi, Hiba Jawdat; Bashir, Nasir Z; Bashiri, Azadeh; Benzian, Habib; Bernabe, Eduardo; Bhagat, Devidas S; Bhojaraja, Vijayalakshmi S; Bjørge, Tone; Bouaoud, Souad; Braithwaite, Dejana; Briko, Nikolay Ivanovich; Calina, Daniela; Carreras, Giulia; Chakraborty, Promit Ananyo; Chattu, Vijay Kumar; Chaurasia, Akhilanand; Chen, Meng Xuan; Cho, William C S; Chu, Dinh-Toi; Chukwu, Isaac Sunday; Chung, Eunice; Cruz-Martins, Natália; Dadras, Omid; Dai, Xiaochen; Dandona, Lalit; Dandona, Rakhi; Daneshpajouhnejad, Parnaz; Darvishi Cheshmeh Soltani, Reza; Darwesh, Aso Mohammad; Debela, Sisay Abebe; Derbew Molla, Meseret; Dessalegn, Fikadu Nugusu; Dianati-Nasab, Mostafa; Digesa, Lankamo Ena; Dixit, Shilpi Gupta; Dixit, Abhinav; Djalalinia, Shirin; El Sayed, Iman; El Tantawi, Maha; Enyew, Daniel Berhanie; Erku, Daniel Asfaw; Ezzeddini, Rana; Fagbamigbe, Adeniyi Francis; Falzone, Luca; Fetensa, Getahun; Fukumoto, Takeshi; Gaewkhiew, Piyada; Gallus, Silvano; Gebrehiwot, Mesfin; Ghashghaee, Ahmad; Gill, Paramjit Singh; Golechha, Mahaveer; Goleij, Pouya; Gomez, Ricardo Santiago; Gorini, Giuseppe; Guimaraes, Andre Luiz Sena; Gupta, Bhawna; Gupta, Sapna; Gupta, Veer Bala; Gupta, Vivek Kumar; Haj-Mirzaian, Arvin; Halboub, Esam S; Halwani, Rabih; Hanif, Asif; Hariyani, Ninuk; Harorani, Mehdi; Hasani, Hamidreza; Hassan, Abbas M; Hassanipour, Soheil; Hassen, Mohammed Bheser; Hay, Simon I; Hayat, Khezar; Herrera-Serna, Brenda Yuliana; Holla, Ramesh; Horita, Nobuyuki; Hosseinzadeh, Mehdi; Hussain, Salman; Ilesanmi, Olayinka Stephen; Ilic, Irena M; Ilic, Milena D; Isola, Gaetano; Jaiswal, Abhishek; Jani, Chinmay T; Javaheri, Tahereh; Jayarajah, Umesh; Jayaram, Shubha; Joseph, Nitin; Kadashetti, Vidya; Kandaswamy, Eswar; Karanth, Shama D; Karaye, Ibraheem M; Kauppila, Joonas H; Kaur, Harkiran; Keykhaei, Mohammad; Khader, Yousef Saleh; Khajuria, Himanshu; Khanali, Javad; Khatib, Mahalaqua Nazli; Khayat Kashani, Hamid Reza; Khazeei Tabari, Mohammad Amin; Kim, Min Seo; Kompani, Farzad; Koohestani, Hamid Reza; Kumar, G Anil; Kurmi, Om P; La Vecchia, Carlo; Lal, Dharmesh Kumar; Landires, Iván; Lasrado, Savita; Ledda, Caterina; Lee, Yo Han; Libra, Massimo; Lim, Stephen S; Listl, Stefan; Lopukhov, Platon D; Mafi, Ahmad R; Mahumud, Rashidul Alam; Malik, Ahmad Azam; Mathur, Manu Raj; Maulud, Sazan Qadir; Meena, Jitendra Kumar; Mehrabi Nasab, Entezar; Mestrovic, Tomislav; Mirfakhraie, Reza; Misganaw, Awoke; Misra, Sanjeev; Mithra, Prasanna; Mohammad, Yousef; Mohammadi, Mokhtar; Mohammadi, Esmaeil; Mokdad, Ali H; Moni, Mohammad Ali; Moraga, Paula; Morrison, Shane Douglas; Mozaffari, Hamid Reza; Mubarik, Sumaira; Murray, Christopher J L; Nair, Tapas Sadasivan; Narasimha Swamy, Sreenivas; Narayana, Aparna Ichalangod; Nassereldine, Hasan; Natto, Zuhair S; Nayak, Biswa Prakash; Negru, Serban Mircea; Nggada, Haruna Asura; Nouraei, Hasti; Nuñez-Samudio, Virginia; Oancea, Bogdan; Olagunju, Andrew T; Omar Bali, Ahmed; Padron-Monedero, Alicia; Padubidri, Jagadish Rao; Pandey, Anamika; Pardhan, Shahina; Patel, Jay; Pezzani, Raffaele; Piracha, Zahra Zahid; Rabiee, Navid; Radhakrishnan, Venkatraman; Radhakrishnan, Raghu Anekal; Rahmani, Amir Masoud; Rahmanian, Vahid; Rao, Chythra R; Rao, Sowmya J; Rath, Goura Kishor; Rawaf, David Laith; Rawaf, Salman; Rawassizadeh, Reza; Razeghinia, Mohammad Sadegh; Rezaei, Nazila; Rezaei, Negar; Rezaei, Nima; Rezapour, Aziz; Riad, Abanoub; Roberts, Thomas J; Romero-Rodríguez, Esperanza; Roshandel, Gholamreza; S, Manjula; S N, Chandan; Saddik, Basema; Saeb, Mohammad Reza; Saeed, Umar; Safaei, Mohsen; Sahebazzamani, Maryam; Sahebkar, Amirhossein; Salek Farrokhi, Amir; Samy, Abdallah M; Santric-Milicevic, Milena M; Sathian, Brijesh; Satpathy, Maheswar; Šekerija, Mario; Senthilkumaran, Subramanian; Seylani, Allen; Shafaat, Omid; Shahsavari, Hamid R; Shamsoddin, Erfan; Sharew, Mequannent Melaku; Sharifi-Rad, Javad; Shetty, Jeevan K; Shivakumar, K M; Shobeiri, Parnian; Shorofi, Seyed Afshin; Shrestha, Sunil; Siddappa Malleshappa, Sudeep K; Singh, Paramdeep; Singh, Jasvinder A; Singh, Garima; Sinha, Dhirendra Narain; Solomon, Yonatan; Suleman, Muhammad; Suliankatchi Abdulkader, Rizwan; Taheri Abkenar, Yasaman; Talaat, Iman M; Tan, Ker-Kan; Tbakhi, Abdelghani; Thiyagarajan, Arulmani; Tiyuri, Amir; Tovani-Palone, Marcos Roberto; Unnikrishnan, Bhaskaran; Vo, Bay; Volovat, Simona Ruxandra; Wang, Cong; Westerman, Ronny; Wickramasinghe, Nuwan Darshana; Xiao, Hong; Yu, Chuanhua; Yuce, Deniz; Yunusa, Ismaeel; Zadnik, Vesna; Zare, Iman; Zhang, Zhi-Jiang; Zoladl, Mohammad; Force, Lisa M; Hugo, Fernando N
IMPORTANCE/UNASSIGNED:Lip, oral, and pharyngeal cancers are important contributors to cancer burden worldwide, and a comprehensive evaluation of their burden globally, regionally, and nationally is crucial for effective policy planning. OBJECTIVE/UNASSIGNED:To analyze the total and risk-attributable burden of lip and oral cavity cancer (LOC) and other pharyngeal cancer (OPC) for 204 countries and territories and by Socio-demographic Index (SDI) using 2019 Global Burden of Diseases, Injuries, and Risk Factors (GBD) Study estimates. EVIDENCE REVIEW/UNASSIGNED:The incidence, mortality, and disability-adjusted life years (DALYs) due to LOC and OPC from 1990 to 2019 were estimated using GBD 2019 methods. The GBD 2019 comparative risk assessment framework was used to estimate the proportion of deaths and DALYs for LOC and OPC attributable to smoking, tobacco, and alcohol consumption in 2019. FINDINGS/UNASSIGNED:In 2019, 370 000 (95% uncertainty interval [UI], 338 000-401 000) cases and 199 000 (95% UI, 181 000-217 000) deaths for LOC and 167 000 (95% UI, 153 000-180 000) cases and 114 000 (95% UI, 103 000-126 000) deaths for OPC were estimated to occur globally, contributing 5.5 million (95% UI, 5.0-6.0 million) and 3.2 million (95% UI, 2.9-3.6 million) DALYs, respectively. From 1990 to 2019, low-middle and low SDI regions consistently showed the highest age-standardized mortality rates due to LOC and OPC, while the high SDI strata exhibited age-standardized incidence rates decreasing for LOC and increasing for OPC. Globally in 2019, smoking had the greatest contribution to risk-attributable OPC deaths for both sexes (55.8% [95% UI, 49.2%-62.0%] of all OPC deaths in male individuals and 17.4% [95% UI, 13.8%-21.2%] of all OPC deaths in female individuals). Smoking and alcohol both contributed to substantial LOC deaths globally among male individuals (42.3% [95% UI, 35.2%-48.6%] and 40.2% [95% UI, 33.3%-46.8%] of all risk-attributable cancer deaths, respectively), while chewing tobacco contributed to the greatest attributable LOC deaths among female individuals (27.6% [95% UI, 21.5%-33.8%]), driven by high risk-attributable burden in South and Southeast Asia. CONCLUSIONS AND RELEVANCE/UNASSIGNED:In this systematic analysis, disparities in LOC and OPC burden existed across the SDI spectrum, and a considerable percentage of burden was attributable to tobacco and alcohol use. These estimates can contribute to an understanding of the distribution and disparities in LOC and OPC burden globally and support cancer control planning efforts.
PMCID:10485745
PMID: 37676656
ISSN: 2374-2445
CID: 5611702

Virtual Tumor Boards for Remote Learning in Head and Neck Surgical Oncology

Papazian, Michael R; Chow, Michael; Weed, Donald; Liu, Jeffrey C; Bewley, Arnaud F; Moore, Michael G; Givi, Babak
IMPORTANCE/UNASSIGNED:In addition to their patient management value, multidisciplinary tumor boards have been recognized as effective learning tools. However, the value of using a virtual tumor board as a learning tool for head and neck surgical oncology fellows has not been studied. OBJECTIVE/UNASSIGNED:To describe the structure and content of the American Head and Neck Society (AHNS) Virtual Tumor Board and assess its educational value as perceived by attendees. DESIGN, SETTING, AND PARTICIPANTS/UNASSIGNED:All sessions of the AHNS Virtual Tumor Board from April 8, 2020, to June 1, 2022, were reviewed. Topics, presenters, participants, and viewership data were collected as of October 15, 2022, from session recordings posted to an online video sharing and social media platform. Additionally, an anonymous, 14-question online survey was designed to elicit feedback from head and neck surgery trainees on virtual tumor board engagement, strengths, and weaknesses. The survey was electronically distributed in June and July 2022 to the 101 fellows enrolled in AHNS-accredited programs between July 1, 2020, and June 30, 2022. MAIN OUTCOMES AND MEASURES/UNASSIGNED:The primary aim was to tabulate online viewership of the sessions. The secondary aim was to qualitatively assess the experience of head and neck trainees with the AHNS Virtual Tumor Board using a survey. RESULTS/UNASSIGNED:Forty-two sessions of the virtual tumor board were held between April 8, 2020, and June 1, 2022. Almost all sessions (41 [98%]) were case based. One hundred and sixteen cases were presented, representing 2 to 3 cases per session, by 75 unique faculty members. Each session was viewed a mean of 217 times (range, 64-2216 views). In the 2021 to 2022 academic year, a mean of 60 viewers (range, 30-92 viewers) attended each live session. In all, 29 survey responses were collected from 101 fellows in AHNS-accredited programs (29% response rate). Most respondents felt the format allowed for excellent teaching (18 of 26 respondents [69%]) and discussion (19 of 26 respondents [73%]). Most respondents (22 of 29 respondents [76%]) believed that practicing head and neck surgeons would benefit from the sessions. CONCLUSIONS AND RELEVANCE/UNASSIGNED:This survey study found that the AHNS Virtual Tumor Board was well-attended and well-reviewed by head and neck surgical oncology trainees. The virtual tumor board format could be used as model of remote learning for other organizations.
PMCID:10450583
PMID: 37615974
ISSN: 2168-619x
CID: 5599382

Dose-Dependent Glucocorticoid Regulation of Transcription Factors in Vocal Fold Fibroblasts and Macrophages

Nakamura, Ryosuke; Bing, Renjie; Gartling, Gary J; Garabedian, Michael J; Branski, Ryan C
OBJECTIVE:Variable outcomes of glucocorticoid (GC) therapy for laryngeal disease are putatively due to diverse interactions of the GC receptor (GR) with cell signaling pathways, limited consideration regarding concentration-dependent effects, and inconsistent selection of GCs. In the current study, we evaluated the concentration-dependent effects of three frequently administered GCs on transcription factors with an emphasis on the phosphorylation of GR at Ser203 and Ser211 regulating the nuclear translocation of GR. This study provides foundational data regarding the diverse functions of GCs to optimize therapeutic approaches. STUDY DESIGN:In vitro. METHODS:Human vocal fold fibroblasts and THP1-derived macrophages were treated with different concentrations of dexamethasone, methylprednisolone, and triamcinolone in combination with IFN-γ, TNF-α, or IL4. Phosphorylated STAT1, NF-κB family molecules, and phosphorylated STAT6 were analyzed by Western blotting. Ser211-phosphorylated GR (S211-pGR) levels relative to GAPDH and Ser203-phosphorylated GR (S203-pGR) were also analyzed. RESULTS:GCs differentially altered phosphorylated STAT1 and NF-κB family molecules in different cell types under IFN-γ and TNF-α stimuli. GCs did not alter phosphorylated STAT6 in IL4-treated macrophages. The three GCs were nearly equivalent. A lower concentration of dexamethasone increased S211-pGR/GAPDH ratios relative to increased S211-pGR/S203-pGR ratios regardless of cell type and treatment. CONCLUSION:The three GCs employed in two cell lines had nearly equivalent effects on transcription factor regulation. Relatively high levels of Ser203-phosphorylation at low GC concentrations may be related to concentration-dependent differential effects of GCs in the two cell lines. LEVEL OF EVIDENCE:NA Laryngoscope, 133:2704-2711, 2023.
PMCID:10406972
PMID: 36752581
ISSN: 1531-4995
CID: 5735082

Private Payer-Negotiated Rates for FDA-Approved Head and Neck Cancer Immunotherapy and Chemotherapy Agents

Talwar, Abhinav; Kim, Sooyoung; Yu, Shun; Samant, Sandeep; Tozan, Yesim; Givi, Babak
OBJECTIVE:To quantify the price that private payers pay hospitals for head and neck squamous cell carcinoma (HNSCC) treatments and identify hospital-level factors associated with price variation. STUDY DESIGN:Cross-sectional study. SETTING:Price transparency files. METHODS:Files from the top 50 hospitals in otolaryngology according to the US News and World Report were analyzed between December 2021 and June 2022. This study analyzed the following Food and Drug Administration-approved HNSCC therapies: pembrolizumab, nivolumab, cetuximab, cisplatin, carboplatin, and paclitaxel. RESULTS:Twenty-four (48%) hospitals reported prices for at least 1 medication in our sample. Newer biologics were significantly more expensive than traditional chemotherapeutic agents. Given approved medication regimens, all biologics in our sample have similar annual costs. Price markups over acquisition costs ranged between 109% (pembrolizumab, nivolumab) and 530% for carboplatin. Across hospitals, prices varied the most for paclitaxel, the cheapest medication in our sample, and prices varied the least for pembrolizumab the most expensive medication in our sample. Hospital 340B status and geographic location in the northeast/west are associated with lower price markups. CONCLUSION:Price nondisclosure remains a significant problem among hospitals. Newer biological medications are more expensive when compared to traditional chemotherapeutic agents. Prices vary significantly across hospitals, with lower price markups observed in 340B hospitals as well as hospitals located in the geographic northeast and west. It remains to be seen if price transparency will lead to more uniform pricing or lower costs of treatments.
PMID: 36856039
ISSN: 1097-6817
CID: 5707882

Paralysis Versus Non-Paralysis Anesthesia for Operative Laryngoscopy: A Randomized Controlled Trial

Yang, Jackie; Crosby, Tyler; Chen, Sophia; Ezeh, Uche C; Patil, Sachi; Kwak, Paul E; Chin, Wanda A; Amin, Milan R
OBJECTIVE:To compare outcomes between two standard-of-care anesthesia regimens for operative laryngoscopy: general anesthesia with a neuromuscular blocking agent (NMBA) versus remifentanil and propofol (non-NMBA). METHODS:This was a prospective, single-blinded, randomized controlled trial at a tertiary care center. Patients were randomized to either anesthesia using rocuronium (NMBA) or with remifentanil/propofol infusion alone (non-NMBA). Intraoperative impressions, anesthesia data, and post-operative patient surveys were collected. RESULTS:Sixty-one patients who underwent suspension laryngoscopy from 2020 to 2022 were included (25 female, 36 male, ranging 20-81 years). Thirty patients were enrolled in the NMBA arm and 31 patients in the non-NMBA arm. Heart rate and mean arterial pressure were higher in the NMBA (p < 0.01). Patients in the non-NMBA group were more likely to require vasopressors (p = 0.04, RR = 3.08 [0.86-11.05]). Surgeons were more frequently satisfied with conditions in the NMBA group (86.7%) compared to the non-NMBA group (58.1%, p < 0.01). Procedures were more likely to be paused due to movement in the non-NMBA group (45.1%) compared to the NMBA group (16.6%, p < 0.03, RR = 2.26 [1.02-4.99]). Patients in the non-NMBA group were more likely to endorse myalgia the week after surgery (44%) compared to the NMBA group (8.3%, p < 0.01) and reported higher average pain levels on a 0-10 pain scale (3.7) compared to the paralysis group (2.0). CONCLUSIONS:Anesthesia with rocuronium was associated with better intraoperative conditions and postoperative pain compared to anesthesia with remifentanil/propofol. Remifentanil/propofol were associated with lower blood pressure and suppression of laryngoscopy-associated tachycardia. LEVEL OF EVIDENCE/METHODS:Level 2 Laryngoscope, 2023.
PMID: 36715102
ISSN: 1531-4995
CID: 5419902

General Principles for the Safe Performance, Training, and Adoption of Ablation Techniques for Benign Thyroid Nodules: An American Thyroid Association Statement

Sinclair, Catherine F; Baek, Jung Hwan; Hands, Kathleen E; Hodak, Steven P; Huber, Timothy C; Hussain, Iram; Lang, Brian Hung-Hin; Noel, Julia E; Papaleontiou, Maria; Patel, Kepal N; Russ, Gilles; Russell, Jonathon; Spiezia, Stefano; Kuo, Jennifer H
PMCID:10611977
PMID: 37642289
ISSN: 1557-9077
CID: 5609202

Determinants of motor neuron functional subtypes important for locomotor speed

D'Elia, Kristen P; Hameedy, Hanna; Goldblatt, Dena; Frazel, Paul; Kriese, Mercer; Zhu, Yunlu; Hamling, Kyla R; Kawakami, Koichi; Liddelow, Shane A; Schoppik, David; Dasen, Jeremy S
Locomotion requires precise control of the strength and speed of muscle contraction and is achieved by recruiting functionally distinct subtypes of motor neurons (MNs). MNs are essential to movement and differentially susceptible in disease, but little is known about how MNs acquire functional subtype-specific features during development. Using single-cell RNA profiling in embryonic and larval zebrafish, we identify novel and conserved molecular signatures for MN functional subtypes and identify genes expressed in both early post-mitotic and mature MNs. Assessing MN development in genetic mutants, we define a molecular program essential for MN functional subtype specification. Two evolutionarily conserved transcription factors, Prdm16 and Mecom, are both functional subtype-specific determinants integral for fast MN development. Loss of prdm16 or mecom causes fast MNs to develop transcriptional profiles and innervation similar to slow MNs. These results reveal the molecular diversity of vertebrate axial MNs and demonstrate that functional subtypes are specified through intrinsic transcriptional codes.
PMCID:10600875
PMID: 37676768
ISSN: 2211-1247
CID: 5607632

De novo assembly and annotation of the singing mouse genome

Smith, Samantha K; Frazel, Paul W; Khodadadi-Jamayran, Alireza; Zappile, Paul; Marier, Christian; Okhovat, Mariam; Brown, Stuart; Long, Michael A; Heguy, Adriana; Phelps, Steven M
BACKGROUND:Developing genomic resources for a diverse range of species is an important step towards understanding the mechanisms underlying complex traits. Specifically, organisms that exhibit unique and accessible phenotypes-of-interest allow researchers to address questions that may be ill-suited to traditional model organisms. We sequenced the genome and transcriptome of Alston's singing mouse (Scotinomys teguina), an emerging model for social cognition and vocal communication. In addition to producing advertisement songs used for mate attraction and male-male competition, these rodents are diurnal, live at high-altitudes, and are obligate insectivores, providing opportunities to explore diverse physiological, ecological, and evolutionary questions. RESULTS:Using PromethION, Illumina, and PacBio sequencing, we produced an annotated genome and transcriptome, which were validated using gene expression and functional enrichment analyses. To assess the usefulness of our assemblies, we performed single nuclei sequencing on cells of the orofacial motor cortex, a brain region implicated in song coordination, identifying 12 cell types. CONCLUSIONS:These resources will provide the opportunity to identify the molecular basis of complex traits in singing mice as well as to contribute data that can be used for large-scale comparative analyses.
PMCID:10521431
PMID: 37749493
ISSN: 1471-2164
CID: 5606392

Sensory cortex plasticity supports auditory social learning

Paraouty, Nihaad; Yao, Justin D; Varnet, Léo; Chou, Chi-Ning; Chung, SueYeon; Sanes, Dan H
Social learning (SL) through experience with conspecifics can facilitate the acquisition of many behaviors. Thus, when Mongolian gerbils are exposed to a demonstrator performing an auditory discrimination task, their subsequent task acquisition is facilitated, even in the absence of visual cues. Here, we show that transient inactivation of auditory cortex (AC) during exposure caused a significant delay in task acquisition during the subsequent practice phase, suggesting that AC activity is necessary for SL. Moreover, social exposure induced an improvement in AC neuron sensitivity to auditory task cues. The magnitude of neural change during exposure correlated with task acquisition during practice. In contrast, exposure to only auditory task cues led to poorer neurometric and behavioral outcomes. Finally, social information during exposure was encoded in the AC of observer animals. Together, our results suggest that auditory SL is supported by AC neuron plasticity occurring during social exposure and prior to behavioral performance.
PMCID:10511464
PMID: 37730696
ISSN: 2041-1723
CID: 5609502

Validity of the American College of Radiology Thyroid Imaging Reporting and Data System in Children

Daniels, Kelly E; Shaffer, Amber D; Garbin, Steven; Squires, Judy H; Vaughan, Kevin G; Viswanathan, Pushpa; Witchel, Selma F; Mollen, Kevin P; Yip, Linwah; Monaco, Sara E; Duvvuri, Umamaheswar; Simons, Jeffrey P
OBJECTIVE:To assess the validity of the American College of Radiology Thyroid Imaging Reporting and Data System (ACR TI-RADS) for evaluating thyroid nodules in children. METHODS:Patients aged <19 years with thyroid nodule(s) evaluated by ultrasound (US) from 2007-2018 at a tertiary children's hospital were included. Two radiologists scored de-identified thyroid US images using ACR TI-RADS (from 1, "benign" to 5, "highly suspicious"). The radiologists recorded size and rated vascularity for each nodule. Ultrasound findings were compared to pathology results (operative cases, n = 91) and clinical follow-up without disease progression (non-operative cases, n = 15). RESULTS:Thyroid images from 115 patients were reviewed. Nine patients were excluded due to the absence of an evaluable nodule. Forty-seven benign and 59 malignant nodules were included. Median age at ultrasound was 15 years (range 0.9-18 years). Twenty (18.9%) patients were male. There was moderate agreement between TI-RADS levels assigned by the two raters (kappa = 0.57, p < 0.001). When the raters' levels were averaged, >3 as the threshold for malignancy correctly categorized the greatest percentage of nodules (68.9%). Eleven (18.6%) malignant nodules received a TI-RADS level of 2 (n = 3) or 3 (n = 8). Sensitivity, specificity, and positive and negative predictive values were 81.4%, 53.2%, 68.6%, and 69.4%, respectively. Although not part of TI-RADS, vascularity was similar between benign and malignant nodules (p = 0.56). CONCLUSION/CONCLUSIONS:In a pediatric population, TI-RADS can help distinguish between benign and malignant nodules with comparable sensitivity and specificity to adults. However, the positive and negative predictive values suggest TI-RADS alone cannot eliminate the need for FNA. LEVEL OF EVIDENCE/METHODS:3 Laryngoscope, 2022.
PMID: 36250584
ISSN: 1531-4995
CID: 5482452