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        <datestamp>2026-09-30T04:47:51Z</datestamp>
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          <dc:title>Table 1_Local control after stereotactic radiation for thyroid cancer: a histology risk-stratified analysis.xlsx</dc:title>
          <dc:creator>Bin Gui (542725)</dc:creator>
          <dc:creator>Jayavignesh Sekar (25141509)</dc:creator>
          <dc:creator>Margaret Locke (25141512)</dc:creator>
          <dc:creator>Shyamali Saha (4611985)</dc:creator>
          <dc:creator>Mitchell Tulchinsky (25141515)</dc:creator>
          <dc:creator>Brianna Jones (25141518)</dc:creator>
          <dc:creator>Nagashree Seetharamu (18336717)</dc:creator>
          <dc:creator>Maged Ghaly (25141521)</dc:creator>
          <dc:subject>Oncology and Carcinogenesis not elsewhere classified</dc:subject>
          <dc:subject>biological equivalent dose</dc:subject>
          <dc:subject>histology -</dc:subject>
          <dc:subject>metastatic thyroid cancer</dc:subject>
          <dc:subject>SBRT (stereotactic body radiation therapy)</dc:subject>
          <dc:subject>thyroid cancer</dc:subject>
          <dc:description>Purpose/Objective(s)&lt;p&gt;Recurrent and metastatic non-anaplastic thyroid cancer has traditionally been considered relatively radioresistant. We evaluated whether anatomic site or histology risk group better predicts local control (LC) following stereotactic radiation therapy (SBRT/SRS).&lt;/p&gt;Materials/Methods&lt;p&gt;We retrospectively reviewed 32 patients with 66 treated lesions (42 skeletal, 24 non-skeletal) treated between 2012 and 2025. Histology was dichotomized into low-risk (papillary, follicular, medullary, Hürthle cell; n=61) and high-risk (poorly differentiated and squamous cell carcinoma; n=5). BED&lt;sub&gt;10&lt;/sub&gt; was calculated using α/β = 10 Gy. LC was defined per RECIST 1.1. Kaplan–Meier and log-rank tests were used. Intra-patient correlation was addressed via generalized estimating equations (GEE) and Cox shared frailty models. A multivariable GEE model included histology risk, site, BED&lt;sub&gt;10&lt;/sub&gt;, PTV volume, prior surgery, and age.&lt;/p&gt;Results&lt;p&gt;Median follow-up was 15.0 months. Six local failures occurred (crude LC 90.9%); 1- and 2-year LC were 96.5% and 87.1%. Histology risk was the dominant determinant: low-risk histology achieved 95.1% crude LC versus 40.0% for high-risk (log-rank p=0.002). In multivariable GEE analysis, low-risk histology was independently associated with LC (OR 158.0, 95% CI 1.72–14,479.7; p=0.028), whereas skeletal site was not (OR 1.07, 95% CI 0.02–51.8; p=0.974). BED&lt;sub&gt;10&lt;/sub&gt; was not associated with LC after adjustment (p=0.752). Skeletal and non-skeletal LC were similar after histology stratification (95.0% vs 95.2% among low-risk). Treatment was well tolerated; no Grade ≥3 radiation toxicity, myelopathy, or fractures occurred.&lt;/p&gt;Conclusion&lt;p&gt;In stereotactic radiation for metastatic non-anaplastic thyroid cancer, histology risk grouping—not anatomic site or dose escalation—is the dominant predictor of local control. These findings support histology-based risk stratification for SRT patient selection.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-30T04:47:51Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fonc.2026.1898567.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_1_Local_control_after_stereotactic_radiation_for_thyroid_cancer_a_histology_risk-stratified_analysis_xlsx/34029714</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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